Kuru
Open accessAbstract
Kuru was the first human transmissible spongiform encephalopathy (TSE) or prion disease identified, occurring in the Fore linguistic group of Papua New Guinea. Kuru was a uniformly fatal cerebellar ataxic syndrome, usually followed by choreiform and athetoid movements. Kuru imposed a strong balancing selection on the Fore population, with individuals homozygous for the 129 Met allele of the gene (PRNP) encoding for prion protein (PrP) being the most susceptible. The decline in the incidence of kuru in the Fore has been attributed to the exhaustion of the susceptible genotype and ultimately by discontinuation of exposure via cannibalism. Neuropathologically, kuru-affected brains were characterized by widespread degeneration of neurons, astroglial and microglial proliferation, and the presence of amyloid plaques. These early findings have been confirmed and extended by recent immunohistochemical studies for the detection of the TSE-specific PrP (PrP). Confocal laser microscopy also showed the concentration of glial fibrillary acidic protein-positive astrocytic processes at the plaque periphery. The fine structure of plaques corresponds to that described earlier by light microscopy. The successful experimental transmission of kuru led to the awareness of its similarity to Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease and formed a background against which the recent epidemics of iatrogenic and variant Creutzfeldt-Jakob disease could be studied.
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Written from the paper’s full text.
TL;DR
Kuru is the first identified human prion disease, a uniformly fatal cerebellar ataxic syndrome in the Fore of Papua New Guinea, transmitted through endocannibalistic mortuary practices and shaped by strong balancing selection at PRNP codon 129. This review synthesizes genetic, anthropological, clinical, and neuropathological evidence showing that kuru behaves like sporadic CJD and that its decline reflected both cessation of exposure and depletion of susceptible genotypes.
Key findings
- Kuru was a uniformly fatal cerebellar ataxic syndrome with tremor and choreiform/athetoid movements, divided into ambulant, sedentary, and terminal stages; duration from prodromal signs to death was about 12 months (range, 3–23 months).
- PRNP codon 129 strongly influenced susceptibility: 129 Met/Met homozygotes had earlier onset and shorter incubation, whereas Met/Val and Val/Val carriers developed kuru later, after incubation periods of 20 years or longer, and many survived; survivors showed almost complete absence of the Met/Met genotype. In 1964–1988, 11 of 16 kuru cases had a 129 Val/Val genotype, and the last 11 known patients (1996–2004) had estimated minimum incubation periods of 34 to 41 years, with 8 of 10 heterozygous at codon 129.
- Experimental transmission succeeded: brain tissue from 3 kuru patients transmitted illness to chimpanzees in 1965; overall, 18 cases transmitted kuru with a transmission rate of 95%, slightly higher than sporadic CJD (87%). Kuru PrPTSE showed type 2 or type 3 patterns, and transgenic mice expressing human PrP 129 valine lacked a transmission barrier to kuru, with kuru behaving like sporadic CJD.
- Neuropathologically, kuru brains showed widespread neuronal degeneration, astroglial and microglial proliferation, and amyloid “kuru plaques” measuring 20–60 Hm (as printed) in diameter, most numerous in the cerebellar granular cell layer, basal ganglia, thalamus, and cerebral cortex; PrPTSE was present in plaques and synaptic/perineuronal sites, with spongiform change in deep cortical layers (III–V) of cingulate, entorhinal, and insular cortices and in the subiculum. The decline of kuru was attributed to discontinuation of exposure via cannibalism and exhaustion of the susceptible genotype, with strong balancing selection at PRNP.
Methods
- Design: This is a narrative review; it does not report primary data collection or systematic review methods.
- Data/sample: It synthesizes published clinical, genetic, anthropological, neuropathological, and transmission studies, including the Kuru Registry, stored brain tissue and DNA specimens, and case series such as 12 cases examined by Klatzo et al, 13 cases by Beck and Daniel, and 11 cases by McLean et al.
- Main analysis: Narrative synthesis and comparison of kuru with sporadic CJD, iatrogenic CJD, variant CJD, and Gerstmann-Sträussler-Scheinker disease; no formal meta-analysis or statistical methods are described.
Limitations
- Stated in the paper: systematic examinations of kuru brains have been performed on only a few dozen cases; ultrastructural data are extremely limited because of severe constraints on obtaining well-fixed material; results on GcAb-Ab genotype prevalence in kuru patients are very difficult to interpret; and the histogenesis of vacuoles is not well understood.
- Evident from the text: as a narrative review, there is no systematic search strategy or quantitative synthesis; conclusions rely on historical, observational, and anthropological accounts, with small case numbers and potential recall or selection biases in the cannibalism and genetic data.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
18 of 98 cited sources checked · 2 supported · 2 flagged · accuracy not yet measured
- Interpretationcitation
The loss of Met/Met genotype and accumulation of alternative alleles in the postepidemic Fore population was indicated by the finding that the PRNP V127V synonymous substitution that showed the highest frequency in the surviving elderly women is part of the 127GG-129VV haplotype.
“The loss of Met/Met genotype and accumulation of alternative alleles in the postepidemic Fore population was also indicated by the finding that the PRNP V127V synonymous substitution that showed the highest frequency in the surviving elderly women is part of the 127GG–129VV haplotype (38).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [38] Mead S Whitfield J Poulter M A novel protective prion protein variant that colocalizes with kuru exposure N Engl J Med 2009 361 2056 65 19923577 source
Split into 2 atoms — 0 confirmed, 1 partially supported, 1 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Premisecitation
In contrast to classical studies, modern PrP immunohistochemistry studies stressed the presence of typical spongiform change, as in sporadic CJD, in deep cortical layers (III-V) of the cingulate, entorhinal and insular cortices, and in the subiculum.
“In contrast to the classical studies described above, both articles stressed the presence of typical spongiform change present, as in sporadic CJD, in deep cortical layers (III–V) of the cingulate, entorhinal and insular cortices, and in the subiculum.”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [76] McLean CA Ironside JW Alpers MP Comparative neuropathology of kuru with the new variant of Creutzfeldt-Jakob disease: Evidence for strain of agent predominating over genotype of host Brain Pathol 1998 8 428 37 PMC8098151 9669694 source
The Abstract (page unavailable) says the authors compared kuru and variant CJD using PrP immunohistochemistry, but it does not describe spongiform change in cortical layers III–V or the named regions. Searches for those layers and regions returned only the Abstract and References; our indexed copy points to a separate PDF for the full text, so the decisive findings may be missing. (LLM, conf=0.74)
Experimental — accuracy not yet measured - cites [77] McLean CA The neuropathology of kuru and variant Creutzfeldt-Jakob disease Phil Trans R Soc 2008 363 3685 87 PMC2735511 18849282 source
The passage on the 11 archival kuru cases (section labeled Abstract; page unavailable) reports spongiform change across cortical areas but explicitly excepts the insular gyri, contrary to the claim of insular involvement. It also does not locate the changes in layers III–V or the subiculum. (LLM, conf=0.78)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Interpretationcitation
The Met/Met genotype depletion in survivors was associated with increased susceptibility of 129 Met/Met carriers, who became early victims of the epidemic and disproportionally died after the shortest incubation time.
“This phenomenon was associated with increased susceptibility of the 129 Met/Met carriers who became early victims of the epidemic, disproportionally dying of the disease after the shortest incubation time (24, 37).”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [24] Cervenakova L Goldfarb L Garruto R Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt-Jakob disease Proc Natl Acad Sci USA 1998 95 13239 41 9789072 PMC23768 source
The Results report that Met/Met kuru patients were overrepresented among younger cases, and the Discussion infers that homozygotes probably had shorter incubation periods than heterozygotes. The paper does not establish increased susceptibility or depletion of Met/Met survivors, and it presents the shorter incubation period as probable rather than measured. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [37] Lee H-S Brown P Cervenakova L Increased susceptibility to kuru of carriers of the PRNP 129 methionine/methionine genotype J Infect Dis 2001 183 192 96 11120925 source
- Findingcitation
Deficit of codon 129 homozygosity was found in elderly females who lived through the epidemic in high-exposure areas and attended multiple mortuary feasts.
“Deficit of codon 129 homozygosity was also found in analysis of elderly females who lived through the epidemic in the high-exposure areas and attended multiple mortuary feasts (38).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [38] Mead S Whitfield J Poulter M A novel protective prion protein variant that colocalizes with kuru exposure N Engl J Med 2009 361 2056 65 19923577 source
The Hardy-Weinberg Equilibrium section reports a marked deficit of codon 129 homozygosity in elderly women from midlevel- and high-exposure zones. The Study Sample and Exposure Index section says an earlier, smaller cohort of older women had attended multiple mortuary feasts, but it does not establish that the women in the expanded high-exposure analysis had each attended multiple feasts. Page numbers are not available in our copy. (LLM, conf=0.83)
Experimental — accuracy not yet measured
- Premisecitation
Neuronal alterations in kuru are totally nonspecific in nature.
“Neuronal alterations observed in many nuclei throughout the neuraxis, the anterior motor neurons of the spinal cord, brainstem, cerebellum, and cerebral cortex were totally nonspecific in nature (64);”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [64] Hainfellner J Liberski PP Guiroy DC Pathology and immunohistochemistry of a kuru brain Brain Pathol 1997 7 547 54 9034563 PMC8098557 source
The Abstract (page unavailable) reports neuronal loss and its distribution but does not say that neuronal alterations were nonspecific. Searches for “totally nonspecific” and for neuronal alterations returned no supporting passage. Our indexed copy points to a separate PDF for the full text, so the decisive discussion may be missing. (LLM, conf=0.74)
Experimental — accuracy not yet measured
- Premisecitation
The most striking neuropathologic feature of kuru is the presence of numerous amyloid plaques, known as kuru plaques.
“The most striking neuropathologic feature of kuru is the presence of numerous amyloid plaques described as “spherical bodies with a rim of radiating filaments” and found in 6 of 12 cases studied by Klatzo et al (62) and in “about three quarters” of the 13 cases of Beck and Daniel (68); they then became known as “kuru plaques” (67, 69–71).”
Quote in the paperNot a substantial claim1 of 6 sources checked- cites [62] Klatzo I Gajdusek DC Pathology of kuru Lab Invest 1959 8 799 847 13665963
- cites [68] Beck E Daniel PM Kuru and scrapie compared: Are they examples of system degeneration? Gajdusek DC Gibbs CJ Jr Alpers MP Slow, Latent, and Temperate Virus Infections Washington, DC US Department of Health, Education, and Welfare 1965 85 93
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [67] Fowler M Robertson EG Observations on kuru. III. Pathological features in five cases Australas Ann Med 1959 8 16 26 13638205 source
- cites [69] Kakulas BA Lecours A-R Gajdusek DC Further observations on the pathology of kuru J Neuropathol Exp Neurol 1967 26 85 97 6022166 source
- cites [70] Scrimgeour EM Masters CL Alpers MP A clinicopathological study of case of kuru J Neurol Sci 1983 59 265 75 6854352 source
- cites [71] Sikorska B Liberski PP Sobów T Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: A comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease Neuropathol Appl Neurobiol 2009 35 46 59 18513219 source
The Introduction discusses kuru plaques, and the Results describe them as amyloid plaques with radiating fibrils. The paper does not establish that they are numerous in kuru or its most striking neuropathologic feature. The indexed passages provide section labels but no page numbers. (LLM, conf=0.83)
Experimental — accuracy not yet measured
- Premisecitation
The occipital cortex is variably affected in kuru.
“The occipital cortex is variably affected (77).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [77] McLean CA The neuropathology of kuru and variant Creutzfeldt-Jakob disease Phil Trans R Soc 2008 363 3685 87 PMC2735511 18849282 source
The passage labeled Abstract (page not provided) says the occipital cortex is an exception to the prominent cortical involvement seen in kuru. It does not say that occipital involvement varies between cases, so it supports differential involvement but not the claimed variability. (LLM, conf=0.79)
Experimental — accuracy not yet measured
- Premisecitation
The Fore still believe that kuru is caused by malicious sorcerers.
“The Fore still believe that kuru is caused by malicious sorcerers”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [52] Whitfield JP Pako WH Collinge J Mortuary rites of the South Fore and kuru Phil Trans R Soc B 2008 363 3721 24 18849288 PMC2581657 source
The Introduction discusses mortuary practices and kuru transmission, while section 3 mentions sorcerers only in describing a person's occult power. Neither passage says that the Fore still believe malicious sorcerers cause kuru. Searches for sorcery, current beliefs, and explanations of kuru found no passage establishing that claim; no page numbers are available in our copy. (LLM, conf=0.75)
Experimental — accuracy not yet measured
- Findingcitation
The fine structure of amyloid plaques from the "K" case corresponds to that described by light microscopy.
“The fine structure of plaques was surprisingly well preserved, and it corresponds to that described by light microscopy (71).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [71] Sikorska B Liberski PP Sobów T Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: A comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease Neuropathol Appl Neurobiol 2009 35 46 59 18513219 source
The Introduction (page unavailable) says the authors compared plaques by light and electron microscopy and proposed that ultrastructural differences in vCJD are reflected in their light-microscopic appearance. The Methods confirm that they examined a kuru case, but the passages found do not say that the fine structure of plaques from the “K” case corresponded to its light-microscopic description or was surprisingly well preserved. (LLM, conf=0.73)
Experimental — accuracy not yet measured
- Findingcitation
The PRNP codon 129 genotype frequency in kuru patients at the height of the epidemic deviated significantly from Fore survivors and non-Fore controls.
“The PRNP codon 129 genotype frequency in kuru patients at the height of the epidemic was found to deviate significantly from Fore survivors and non-Fore controls.”
Quote in the paperSubstantial claim - Findingcitation
The Met/Met genotype depletion in the group of survivors was significant as compared with the healthy population of non-Fore villages sampled during the same 1957-1959 period.
“The Met/Met genotype depletion in the group of survivors was significant as compared with the healthy population of non-Fore villages sampled during the same 1957–1959 period.”
Quote in the paperSubstantial claim - Findingcitation
A group of individuals who lived through the kuru epidemic and never developed the disease deviated from Hardy-Weinberg equilibrium because of almost complete absence of the Met/Met genotype at position 129.
“A group of individuals who lived through the kuru epidemic and never developed the disease was found to deviate from Hardy-Weinberg equilibrium because of almost complete absence of the Met/Met genotype at position 129 (37).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [37] Lee H-S Brown P Cervenakova L Increased susceptibility to kuru of carriers of the PRNP 129 methionine/methionine genotype J Infect Dis 2001 183 192 96 11120925 source
- Findingcitation
11 of 16 kuru cases that occurred in 1964-1988 had a 129 Val/Val genotype.
“Indeed, 11 of 16 kuru cases that occurred in 1964–1988 had a 129 Val/Val genotype (and unpublished data) (40–42).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [40] Mead S Stumpf MP Whitfield J Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics Science 2003 300 640 43 12690204 source
- cites [41] Hardy J Scholz S Evans W Prion genotypes in Central America suggest selection for the V129 allele Am J Med Genet B Neuropsychiatr Genet 2006 141B 33 35 16287045 source
- cites [42] Lindenbaum S Kuru Sorcery. Disease and Danger in the New Guinea Highlands Palo Alto, CA Mayfield Publishing Company 1979
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Findingcitation
The last 11 known kuru patients studied at the very end of the epidemic (1996-2004) had an estimated minimum incubation period of 34 to 41 years.
“The last 11 known kuru patients studied at the very end of the epidemic (1996–2004) had an estimated minimum incubation period of 34 to 41 years; 8 of 10 were heterozygous at the PRNP codon 129 (39).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [39] Collinge CJ Whitfield J McKintosh E Kuru in the 21st century—An acquired human prion disease with very long incubation periods Lancet 2006 367 2068 74 16798390 source
- Findingreasoning
Many Met/Val and Val/Val genotype carriers survived the kuru epidemic altogether.
“Many of the Met/Val and Val/Val genotype carriers survived the epidemic altogether, demonstrating a lower susceptibility to kuru.”
Quote in the paperSubstantial claim - Findingcitation
8 of 10 of the last known kuru patients studied at the very end of the epidemic (1996-2004) were heterozygous at the PRNP codon 129.
“The last 11 known kuru patients studied at the very end of the epidemic (1996–2004) had an estimated minimum incubation period of 34 to 41 years; 8 of 10 were heterozygous at the PRNP codon 129 (39).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [39] Collinge CJ Whitfield J McKintosh E Kuru in the 21st century—An acquired human prion disease with very long incubation periods Lancet 2006 367 2068 74 16798390 source
- Findingnone given
Larger confluent vacuoles were visible in the caudate nuclei.
“Larger confluent vacuoles were visible in the caudate nuclei.”
Quote in the paperNot a substantial claim - Findingnone given
We observed no colocalization of PrPd and β-amyloid precursor protein either inside the plaques or in the neuropil.
“We observed no colocalization of PrPd and β-amyloid precursor protein either inside the plaques or in the neuropil.”
Quote in the paperNot a substantial claim - Findingcitation
Vacuoles are formed relatively abruptly with no detectable transitional stages.
“We suggested that vacuoles are formed relatively abruptly with no detectable transitional stages (Gibson and Liberski, unpublished data).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Gibson and Liberski, unpublished data
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Findingown data
Immunochemistry using antibodies against phosphorylated epitopes of neurofilaments showed loss of axons in the cerebellum that was more severe than in other prion diseases.
“Immunochemistry using antibodies against phosphorylated epitopes of neurofilaments showed loss of axons in the cerebellum that was more severe than in other prion diseases.”
Quote in the paperNot a substantial claim - Findingown data
The fine structure of amyloid plaques from the "K" case was surprisingly well preserved.
“The fine structure of plaques was surprisingly well preserved, and it corresponds to that described by light microscopy (71).”
Quote in the paperNot a substantial claim - Findingown data
Confocal laser microscopy confirmed the concentration of GFAP-positive astrocytic processes at the plaque periphery.
“Confocal laser microscopy confirmed the concentration of GFAP-positive astrocytic processes at the plaque periphery.”
Quote in the paperNot a substantial claim - Findingown data
There was no colocalization of MAP-tau and PrPSc.
“There was no colocalization of MAP-tau and PrPSc.”
Quote in the paperNot a substantial claim - Findingown data
Immunohistochemistry for HLA-DR revealed the presence of positive cells around kuru plaques.
“Immunohistochemistry for HLA-DR revealed the presence of positive cells around kuru plaques.”
Quote in the paperNot a substantial claim - Findingnone given
In the cerebellum of a kuru case, plaques were seen in granular cell layers but were not that numerous.
“In the cerebellum, plaques were seen in granular cell layers but were not that numerous.”
Quote in the paperNot a substantial claim - Premisecitation
Two kuru patients were homozygous at position 129 of the PRNP gene.
“An incidental finding indicating that 2 kuru patients were homozygous at position 129 of the PRNP gene was reported (34) and subsequently confirmed (35), prompting further research on the susceptibility to kuru.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [34] Goldfarb LG Brown P Goldgaber D Patients with Creutzfeldt-Jakob disease and kuru lack the mutation in the PRIP gene found in Gersrmann-Sträussler syndrome, but they show a different double-allele mutation in the same gene Am J Hum Genet 1989 45 Suppl A189
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [35] Goldfarb LG Brown P Gajdusek DC The molecular genetics of human transmissible spongiform encephalopathy Prusiner SB Collinge J Powell J Anderton B Prion Diseases of Humans and Animals Chichester, UK Ellis Horwood 1992 139 53
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Many kuru victims were not closely related biologically but were considered by the Fore to be kin in a social sense.
“Many kuru victims were not closely related biologically but were considered by the Fore to be kin in what we would call a “social sense.””
Quote in the paperSubstantial claim - Interpretationreasoning
Met/Val and Val/Val genotype carriers have a lower susceptibility to kuru.
“Many of the Met/Val and Val/Val genotype carriers survived the epidemic altogether, demonstrating a lower susceptibility to kuru.”
Quote in the paperSubstantial claim - Premisecitation
Body parts were allocated according to kinship rights and gender.
“Body parts were allocated according to kinship rights and gender.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
The relationship between kuru and cannibalism seemed to be confirmed by the rules for the consumption of human flesh, which tallied with the epidemiological evidence.
“The relationship between kuru and cannibalism seemed to be confirmed by the rules for the consumption of human flesh, which tallied with the epidemiological evidence.”
Quote in the paperSubstantial claim - Interpretationcitation
In the group of young Fore males just entering the age of risk, Met/Met individuals were preferentially affected with kuru.
“The results of this analysis demonstrate that in the group of young Fore males just entering the age of risk, the Met/Met individuals were preferentially affected with kuru (37).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [37] Lee H-S Brown P Cervenakova L Increased susceptibility to kuru of carriers of the PRNP 129 methionine/methionine genotype J Infect Dis 2001 183 192 96 11120925 source
- Premisecitation
The daughters-in-law of a deceased man or woman usually requested the head.
“the daughters-in-law of a deceased man or woman usually requested the head.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationnone given
The exposure to kuru disappeared because of an Australian "carrot-and-stick" approach to the practice of cannibalism rather than by any biological or medical reason.
“However, the exposure disappeared because of an Australian “carrot-and-stick” approach to the practice of cannibalism rather than by any biological or medical reason!”
Quote in the paperNot a substantial claim - Premisereasoning
Not all the Fore were cannibals.
“Significantly, not all the Fore were cannibals.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [46] Glasse RM Lindenbaum S Kuru at Wanitabe Hornabrook RW Essays on Kuru Berks. E. W. Classey Faringdon, Oxon, UK 1976 38 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Not all deceased persons were eaten.
“Not all deceased persons were eaten.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
South Fore children, living in houses with their mothers, ate what their mothers gave them.
“South Fore children, living in houses with their mothers, ate what their mothers gave them.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [46] Glasse RM Lindenbaum S Kuru at Wanitabe Hornabrook RW Essays on Kuru Berks. E. W. Classey Faringdon, Oxon, UK 1976 38 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
Kuru imposed a strong balancing selection on the Fore population.
“Kuru imposed a strong balancing selection on the Fore population (40).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [40] Mead S Stumpf MP Whitfield J Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics Science 2003 300 640 43 12690204 source
- Premisecitation
Kuru victims were viewed favorably, especially if the body was not emaciated.
“kuru victims were viewed favorably, especially if the body was not emaciated.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisenone given
Beyond the Fore, the practice was to consume enemies (exocannibalism), not deceased kin (endocannibalism), the Fore pattern.
“Beyond the Fore, the practice was to consume enemies (exocannibalism), not deceased kin (endocannibalism), the Fore pattern.”
Quote in the paperSubstantial claim - Interpretationreasoning
The kuru epidemic eventually began absorbing the less susceptible Met/Val and Val/Val genotypes prevailing in the region, after having used up the more susceptible Met/Met genotype.
“Having “used up” the more susceptible Met/Met genotype, the kuru epidemic eventually began absorbing the less susceptible Met/Val and Val/Val genotypes prevailing in the region.”
Quote in the paperSubstantial claim - Premisereasoning
Anthropological studies by Robert Glasse and Shirley Lindenbaum indicated that the genetic hypothesis for kuru was not tenable.
“Anthropological studies by Robert Glasse and Shirley Lindenbaum soon indicated that the genetic hypothesis was not tenable.”
Quote in the paperSubstantial claim - Interpretationcitation
Lack of 129 Met/Met individuals in the postepidemic population control may be explained by the massive loss of this genotype to kuru in a small population.
“Lack of the 129 Met/Met individuals in the postepidemic population control may be explained by the massive loss of this genotype to kuru in a small population (37).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [37] Lee H-S Brown P Cervenakova L Increased susceptibility to kuru of carriers of the PRNP 129 methionine/methionine genotype J Infect Dis 2001 183 192 96 11120925 source
- Interpretationreasoning
Male children had less exposure to the kuru agent than their sisters who continued to live with their mothers.
“Male children thus had less exposure to the kuru agent than their sisters who continued to live with their mothers.”
Quote in the paperNot a substantial claim - Premisecitation
Those who did eat human flesh avoided eating the bodies of women, the main kuru victims.
“those who did avoided eating the bodies of women, the main kuru victims.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [46] Glasse RM Lindenbaum S Kuru at Wanitabe Hornabrook RW Essays on Kuru Berks. E. W. Classey Faringdon, Oxon, UK 1976 38 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
All body parts were eaten except the gallbladder, which was considered too bitter.
“All body parts were eaten except the gallbladder, which was considered too bitter.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The first systematic examination of kuru neuropathology, comprising 12 cases, was published by Klatzo et al in 1959.
“The first systematic examination of kuru neuropathology (12 cases) was published by Klatzo et al (62) in 1959 (Table).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Klatzo et al (62)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
The position that cannibalism was not a socially approved custom in Papua New Guinea is no longer accepted.
“a position that is no longer accepted.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [53] Arens W The Man-Eating Myth New York, NY Oxford University Press 1979
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [54] Knauft BM Good Company and Violence. Sorcery and Social Action in a Lowland New Guinea Society Berkeley, CA University of California Press 1985
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [55] Gillison G Between Culture and Fantasy A New Guinea Highlands Mythology Chicago, IL Chicago University Press 1993
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
In the striatum of kuru cases, some neurons are vacuolated to a degree that they look "moth-eaten".
“In the striatum, some neurons were vacuolated to such a degree that they looked “moth-eaten” (“a group of bubbles” [69]).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [69] Kakulas BA Lecours A-R Gajdusek DC Further observations on the pathology of kuru J Neuropathol Exp Neurol 1967 26 85 97 6022166 source
- Interpretationcitation
Kuru first arose after a single individual with CJD was consumed.
“It is now thought that kuru first arose after a single individual with CJD was consumed”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [49] Alpers MP Rail L Kuru and Creutzfeldt-Jakob disease: Clinical and etiological aspects Proceedings of the Australian Association of Neurologists 1971 8 7 15 5005124
- Premisenone given
Systematic neuropathological examinations of kuru brains have been performed on only a few dozen cases.
“Surprisingly, systematic examinations of kuru brains have been performed on only a few dozen cases (Figs. 2–4).”
Quote in the paperNot a substantial claim - Interpretationcitation
The location of PrPTSE in the spinal cord substantia gelatinosa in kuru is reminiscent of that typical of iatrogenic CJD cases after peripheral inoculation.
“The latter location was reminiscent of that typical of iatrogenic CJD cases after peripheral inoculation (78).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [78] Goodbrand IA Ironside JW Nicolson D Prion protein accumulations in the spinal cords of patients with sporadic and growth hormone-associated Creutzfeldt-Jakob disease Neurosci Lett 1995 183 127 30 7746471 source
- Premisecitation
Kuru plaques were found in 6 of 12 cases studied by Klatzo et al.
“found in 6 of 12 cases studied by Klatzo et al (62)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [62] Klatzo I Gajdusek DC Pathology of kuru Lab Invest 1959 8 799 847 13665963
- Interpretationcitation
The latter kuru case is neuropathologically most similar to type 2 or 3 129 MV type of CJD of the Collinge et al classification or type 2 CJD of the Parchi et al classification.
“The latter case has been neuropathologically compared with known subtypes of CJD and it seems the most similar to type 2 or 3 129 MV type of CJD of the Collinge et al (80) classification or type 2 CJD of the Parchi et al (22) classification.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [80] Collinge J Sidle KCL Meads J Molecular analysis of prion strain variation and the etiology of new variant CJD Nature 1996 383 685 70 8878476 source
- cites [22] Parchi P Castellani R Capellari S Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease Ann Neurol 1996 39 767 78 8651649 source
- Interpretationown data
The finding of dispersed β-amyloid precursor protein-positive processes is consistent with the presence of dystrophic neurites at the periphery of kuru plaques in kuru and sporadic CJD, as seen by electron microscopy.
“This finding is consistent with the presence of dystrophic neurites at the periphery of kuru plaques in kuru and sporadic CJD, as seen by electron microscopy.”
Quote in the paperNot a substantial claim - Premisecitation
Lampert's work preceded the current view that autophagy is one of the most important phenomena observed in all prion diseases.
“Thus, Lampert’s work preceded the current view that autophagy is one of the most important phenomena observed in all prion diseases (87, 88).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [87] Liberski PP Sikorska B Bratosiewicz-Wasik J Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: From apoptosis to autophagy Int J Biochem Cell Biol 2004 36 2473 90 15325586 source
- cites [88] Arstila AU Trump BF Studies on cellular autophagocytosis. The formation of autophagic vacuoles in the liver after glucagon administration Am J Pathol 1968 53 687 733 4300890 PMC2013521
- Premisecitation
Field et al. used formalin-fixed brains of 5 kuru cases to demonstrate degeneration of Purkinje cells, torpedo formation, and proliferation of Bergmann glia.
“Field et al (81) used formalin-fixed brains of 5 kuru cases to demonstrate degeneration of Purkinje cells, torpedo formation, and proliferation of Bergmann glia.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [81] Field EJ Mathews JD Raine CS Electron microscopic observations on the cerebellar cortex in kuru J Neurol Sci 1969 8 209 24 4185060 source
- May combine two claims. 38
- Classified as probably not a substantial claim. 25
- The quote only partly states this claim. 2
May combine two claims.
Findingcitation129 Met/Val and Val/Val carriers developed kuru at a later age, after an incubation period of 20 years or longer, and many survived the epidemic.
“Based on representative statistics, it was concluded that individuals homozygous for the 129 Met allele had an earlier age of disease onset and a shorter incubation time, whereas 129 Met/Val and Val/Val carriers developed kuru at a later age, after an incubation period of 20 years or longer, and many survived the epidemic (24).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [24] Cervenakova L Goldfarb L Garruto R Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt-Jakob disease Proc Natl Acad Sci USA 1998 95 13239 41 9789072 PMC23768 source
The Results (page not provided) show that Met/Val patients were overrepresented in older age groups, and the Discussion infers that heterozygotes probably had longer incubation periods than homozygotes. The Results do not show later onset for Val/Val patients; Table 1 includes more Val/Val cases under age 15 than over age 30. The paper does not establish an incubation period of 20 years or longer or report that many carriers survived the epidemic. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
FindingcitationIndividuals homozygous for the 129 Met allele had an earlier age of disease onset and a shorter incubation time.
“Based on representative statistics, it was concluded that individuals homozygous for the 129 Met allele had an earlier age of disease onset and a shorter incubation time, whereas 129 Met/Val and Val/Val carriers developed kuru at a later age, after an incubation period of 20 years or longer, and many survived the epidemic (24).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [24] Cervenakova L Goldfarb L Garruto R Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt-Jakob disease Proc Natl Acad Sci USA 1998 95 13239 41 9789072 PMC23768 source
The Results report that Met/Met kuru patients were overrepresented at younger ages of onset, while the Discussion infers that homozygotes probably had a shorter incubation period than heterozygotes. The claim presents that inference as certain. The Results do not support grouping Val/Val carriers with Met/Val carriers as developing kuru later, and the paper does not establish a 20-year incubation period or that many carriers survived the epidemic. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationThe Fore did not talk about rubbing their bodies with brain tissue when describing earlier events and have recently denied the practice.
“However, the Fore did not talk about rubbing their bodies with brain tissue when describing earlier events and have recently denied the practice (52).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [52] Whitfield JP Pako WH Collinge J Mortuary rites of the South Fore and kuru Phil Trans R Soc B 2008 363 3721 24 18849288 PMC2581657 source
The Introduction (page unavailable) concludes that intentional rubbing of brain tissue on mourners did not occur, and §5 says it was never rubbed on their bodies. These passages support the paper’s account of the practice, but do not establish the specific claims that the Fore omitted it when describing earlier events or recently denied it. (LLM, conf=0.83)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationA recent investigation of Fore mortuary practices has shown that, by consuming deceased relatives, the Fore were ensuring that the souls of the departed reached the land of the dead, to be reborn as ancestors.
“A recent investigation of Fore mortuary practices has shown that, by consuming deceased relatives, the Fore were ensuring that the souls of the departed reached the land of the dead, to be reborn as ancestors (52).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [52] Whitfield JP Pako WH Collinge J Mortuary rites of the South Fore and kuru Phil Trans R Soc B 2008 363 3721 24 18849288 PMC2581657 source
May combine two claims.
PremisecitationKuru is a uniformly fatal and remarkably stereotyped cerebellar ataxic syndrome accompanied by tremor and choreiform and athetoid movements.
“Kuru is a uniformly fatal and remarkably stereotyped cerebellar ataxic syndrome accompanied by tremor and choreiform and athetoid movements (27, 39, 57–61)”
Quote in the paperNot a substantial claim2 of 7 sources checked- cites [27] Gajdusek DC Zigas V Degenerative disease of the central nervous system in New Guinea. The endemic occurrence of “kuru” in the native population N Engl J Med 1957 257 974 78 13483871 source
- cites [39] Collinge CJ Whitfield J McKintosh E Kuru in the 21st century—An acquired human prion disease with very long incubation periods Lancet 2006 367 2068 74 16798390 source
- cites [57] Alpers MP Kuru: Age and Duration Studies Adelaide Department of Medicine 1964 12
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [58] Beasley A Fore experiences on the kuru patrols Oceania 2009 79 34 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [59] Collinge CJ Whitfield J McKintosch E A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea Phil Trans R Soc B 2008 363 3725 39 18849289 PMC2581654 source
The Introduction (page unavailable) describes progressive cerebellar ataxia, a well-characterized clinical progression, usually present tremor, and eventual death. It says athetoid and choreiform movements *may occur*, rather than presenting them as invariable accompaniments of kuru. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [60] Collinge J Lessons of kuru research: Background to recent studies with some personal reflections Phil Trans R Soc B 2008 363 3689 96 18849283 PMC2577136 source
The paper’s Abstract describes people dying of kuru and notes clinical similarities between kuru and variant CJD. It does not describe kuru as a stereotyped cerebellar ataxic syndrome or specify tremor, choreiform movements, or athetoid movements; nor does it establish that the disease is uniformly fatal. (LLM, conf=0.72)
Experimental — accuracy not yet measured - cites [61] Prusiner SB Gajdusek DC Alpers MP Kuru with incubation periods exceeding two decades Ann Neurol 1982 12 1 9 7114816 source
May combine two claims.
PremisecitationImmunohistochemical studies revealed that PrPTSE is present not only as kuru plaques but also in synaptic and perineuronal sites and in the spinal cord within substantia gelatinosa in kuru.
“Immunohistochemical studies revealed that PrPTSE was present not only as kuru plaques but also in synaptic and perineuronal sites (64) and in the spinal cord within substantia gelatinosa.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [64] Hainfellner J Liberski PP Guiroy DC Pathology and immunohistochemistry of a kuru brain Brain Pathol 1997 7 547 54 9034563 PMC8098557 source
The Abstract (no page given) reports anti-PrP immunocytochemistry in a kuru brain and describes both diffuse synaptic-type deposits and plaques. Our copy does not report perineuronal deposits or PrP in the spinal cord’s substantia gelatinosa; searches for those sites returned no supporting passage. (LLM, conf=0.86)
Experimental — accuracy not yet measured
May combine two claims.
FindingcitationIn our previous study on amyloid plaques in prion diseases, we demonstrated that kuru plaques morphologically and ultrastructurally resemble those characteristic of sporadic CJD subtype 3 according to the Parchi and Gambetti classification but are remarkably different from florid plaques in variant CJD and multicentric plaques in GSS.
“In our previous study on amyloid plaques encountered in prion diseases (71), we demonstrated that kuru plaques morphologically and ultrastructurally resemble those that are characteristic of sporadic CJD subtype 3 according to the Parchi and Gambetti classification (22) but were remarkably different from florid plaques in variant CJD and multicentric plaques in GSS.”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [71] Sikorska B Liberski PP Sobów T Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: A comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease Neuropathol Appl Neurobiol 2009 35 46 59 18513219 source
- cites [22] Parchi P Castellani R Capellari S Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease Ann Neurol 1996 39 767 78 8651649 source
May combine two claims.
FindingcitationMost young Fore males who developed kuru in 1957-1959 were Met/Met homozygous, whereas survivors exposed at the same age completely lacked the Met/Met genotype.
“Most of the young Fore males who developed kuru in 1957–1959 were Met/Met homozygous, whereas survivors of the kuru epidemic who were exposed to the infection at the same age completely lacked the Met/Met genotype.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataIn the frontal cortex of a kuru case, spongiform change was of moderate intensity, and GFAP-immunoreactive astrocytes were present.
“In the frontal cortex, spongiform change was of moderate intensity, and glial fibrillary acidic protein (GFAP)–immunoreactive astrocytes were present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.
Findingown dataDystrophic neurites were occasionally seen in the vicinity of amyloid plaques.
“Occasionally, dystrophic neurites were seen in the vicinity.”
Quote in the paperNot a substantial claimThe quote only partly states this claim.
Findingown dataPrPTSE immunohistochemistry revealed mostly synaptic deposits and plaques of varying size and shape in the frontal cortex.
“The PrPTSE immunohistochemistry revealed mostly synaptic deposits and plaques of varying size and shape.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn kuru and sporadic CJD, minimal immunoreactivity of MAP-tau was observed at the periphery of the plaques; this pattern differs from variant CJD and GSS, in which MAP-tau expression was much more robust.
“In kuru and sporadic CJD, minimal immunoreactivity of MAP-tau was observed at the periphery of the plaques, that is, again, the pattern of MAP-tau immunoreactivity was different from that of variant CJD and GSS, in which the expression of this protein was much more robust.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn kuru, in contrast to plaques in variant CJD and GSS, GFAP-positive astrocytic cell processes are observed around plaques and at the peripheral part of plaques; this phenomenon is seen, albeit to a slightly lesser degree, in sporadic CJD.
“Moreover, in kuru, in contrast to plaques in variant CJD and GSS, we observed GFAP-positive astrocytic cell processes around plaques and at the peripheral part of plaques. This phenomenon was seen, albeit to a slightly lesser degree, in sporadic CJD.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataIn kuru and sporadic CJD, some distended β-amyloid precursor protein-positive processes were observed, but they were dispersed throughout the cortex and not around the plaques.
“In kuru and sporadic CJD, we also observed some distended β-amyloid precursor protein–positive processes, but they were dispersed throughout the cortex and not around the plaques.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingnone givenFrom examination of the chimpanzee infected with the "K" kuru brain, typical autophagic vacuoles were illustrated, but the process was not mentioned.
“From examination of the chimpanzee infected with the “K” kuru brain, the typical autophagic vacuoles were illustrated, but the process was not mentioned.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMultiple mutations in the PRNP gene have been linked to various phenotypes of hereditary, sporadic, and iatrogenic CJD.
“Multiple mutations in the PRNP gene have been linked to various phenotypes of hereditary, sporadic, and iatrogenic CJD (25, 26).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [25] Palmer MS Dryden AJ Hughes JT Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease Nature 1991 352 340 42 1677164 source
- cites [26] Collinge J Palmer MS Dryden AJ Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease Lancet 1991 337 1441 42 1675319 source
May combine two claims.
InterpretationreasoningThe decline of kuru incidence in the Fore was determined by the discontinuation of exposure and additionally by the exhaustion of the susceptible genotype.
“Apparently, the decline of kuru incidence in the Fore was determined by the discontinuation of exposure and additionally by the exhaustion of the susceptible genotype.”
Quote in the paperSubstantial claimMay combine two claims.
PremisereasoningCannibalism was no longer present in the 1960s, had been suppressed by the government and missions, but the Fore spoke openly about their practice of consuming deceased relatives.
“No longer present in the 1960s, cannibalism had been suppressed by the government and missions, but the Fore spoke openly about their practice of consuming deceased relatives.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationThe disease was judged to be too common and too fatal to be a purely genetic disorder, unless the hypothetical kuru gene was maintained at high frequency by a mechanism of balanced polymorphism for which, at that time, there was no evidence.
“However, the disease was judged to be too common and too fatal to be a purely genetic disorder, unless the hypothetical kuru gene was maintained at high frequency by a mechanism of balanced polymorphism for which, at that time, there was no evidence (44).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [44] Mathews JD Kuru: A Puzzle in Culture and Environmental Medicine PhD thesis University of Melbourne Melbourne, Victoria, Australia 1971
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationThose who died of dysentery, leprosy, and possibly yaws were not consumed.
“Those who died of dysentery, leprosy, and possibly yaws were not consumed”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
InterpretationreasoningCannibalism continued longer in the south, the area with the highest incidence of kuru in the 1960s.
“Cannibalism thus continued longer in the south, the area with the highest incidence of kuru in the 1960s.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenThe first government patrols in the late 1940s had reported cannibalism to be customary throughout much of the region.
“The first government patrols in the late 1940s had also reported cannibalism to be customary throughout much of the region.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationInitiated youths moved to the men's house at approximately age 12 years, leaving behind the world of immaturity, femininity, and cannibalism.
“Initiated youths moved to the men’s house at approximately age 12 years, leaving behind the world of immaturity, femininity, and cannibalism.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationSmall children were never given meat and were also kept away from the ceremony.
“Small children were never given meat and were also kept away from the ceremony.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationBrain tissue mixed with wild green vegetables was cooked in bamboo tubes, which the daughters-in-law shared with other women.
“Brain tissue mixed with wild green vegetables was cooked in bamboo tubes, which the daughters-in-law shared with other women (45).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Classified as probably not a substantial claim.
Premisenone givenThe South Fore reported that some people had continued to hide and eat deceased kin until the road reached them.
“Nevertheless, the South Fore reported that some people had continued to hide and eat deceased kin until the road reached them.”
Quote in the paperSubstantial claimMay combine two claims.
PremisereasoningNearby or distant Fore immigrant groups were welcomed and, in time, were said to possess "one blood" and to stem from a common ancestor.
“Nearby or distant Fore immigrant groups were welcomed and, in time, were said to possess “one blood” and to stem from a common ancestor.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenThe Fore could name those who had died of kuru and those who had participated in the consumption of the deceased person, which allowed for an account of the appearance of the disease in particular hamlets some 4 to 20 years after ingestion.
“Moreover, the Fore could name those who had died of kuru and those who had participated in the consumption of the deceased person, which allowed for an account of the appearance of the disease in particular hamlets some 4 to 20 years after ingestion.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationAdult men in the North Fore consumed the dead more frequently than in the South, where adult men rarely ate human flesh.
“Adult men in the North Fore consumed the dead more frequently than in the South, where adult men rarely ate human flesh”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [46] Glasse RM Lindenbaum S Kuru at Wanitabe Hornabrook RW Essays on Kuru Berks. E. W. Classey Faringdon, Oxon, UK 1976 38 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationFemale relatives by marriage, who were the main consumers, could also request certain body parts.
“Female relatives by marriage, who were the main consumers, could also request certain body parts.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Whitfield JT Mortuary Practices, Genetics and Other Factors Relevant to the Transmission of Kuru in Papua New Guinea PhD dissertation University College London, UK 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationA balancing selection at the PRNP locus somewhat similar to what occurred in the Fore was discovered in some other world populations and has been interpreted as evidence of selection pressure from possible epidemics of prion diseases in prehistoric humans.
“Surprisingly, a balancing selection at the PRNP locus somewhat similar to what occurred in the Fore was discovered in some other world populations and has been interpreted as evidence of selection pressure from possible epidemics of prion diseases in prehistoric humans (40, 41).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [40] Mead S Stumpf MP Whitfield J Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics Science 2003 300 640 43 12690204 source
- cites [41] Hardy J Scholz S Evans W Prion genotypes in Central America suggest selection for the V129 allele Am J Med Genet B Neuropsychiatr Genet 2006 141B 33 35 16287045 source
May combine two claims.
PremisecitationFore genealogies gave legitimacy to ties based on culturally defined notions of kinship, providing a moral guide for living but were not reliable statements of genetic proximity.
“Fore genealogies gave legitimacy to ties based on culturally defined notions of kinship, providing a moral guide for living but were not reliable statements of genetic proximity (42).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [42] Lindenbaum S Kuru Sorcery. Disease and Danger in the New Guinea Highlands Palo Alto, CA Mayfield Publishing Company 1979
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe duration of kuru, as measured from the onset of prodromal signs and symptoms until death, was about 12 months (range, 3-23 months).
“The duration of kuru, as measured from the onset of prodromal signs and symptoms until death, was about 12 months (range, 3–23 months) (54, 62).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [54] Knauft BM Good Company and Violence. Sorcery and Social Action in a Lowland New Guinea Society Berkeley, CA University of California Press 1985
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [62] Klatzo I Gajdusek DC Pathology of kuru Lab Invest 1959 8 799 847 13665963
May combine two claims.
Premisenone givenDeep reflexes were increased, but the plantar reflex was still flexor and the Babinski sign has never been seen.
“Deep reflexes were increased, but the plantar reflex was still flexor and the Babinski sign has never been seen.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe Romberg sign was almost always negative (2 of 34 kuru cases in Alpers' series), but with disease progression, ataxia became marked and the Romberg sign became positive.
“The Romberg sign was almost always negative (2 of 34 kuru cases in Alpers’ series [63]), but with disease progression, ataxia became marked and the Romberg sign became positive.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Alpers MP Kuru: A Clinical Study Washington, DC US Department of Health, Education, and Welfare 1964 1 38
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
InterpretationreasoningThe infectious agent was then recycled through the consumption of those who had died of the disease, amplifying the infectious agent and resulting in the epidemic.
“The infectious agent was then recycled through the consumption of those who had died of the disease, amplifying the infectious agent and resulting in the epidemic.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationConsumption of human flesh and exposure to the infectious agent was limited to adult women, children of both sexes, and a few adult men, matching the epidemiology of kuru in the 1960s.
“Consumption of human flesh and exposure to the infectious agent was thus limited to adult women, children of both sexes, and a few adult men, matching the epidemiology of kuru in the 1960s (46).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [46] Glasse RM Lindenbaum S Kuru at Wanitabe Hornabrook RW Essays on Kuru Berks. E. W. Classey Faringdon, Oxon, UK 1976 38 52
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Premisenone givenIn the third stage, the patient was bedridden, incontinent, and covered with urine and feces, with dysphasia and primitive reflexes, and eventually succumbed in a state of severe emaciation, generalized muscle wasting, and fasciculation, spontaneous or evoked by tapping.
“In the third stage, the patient was bedridden, incontinent, and covered with urine and feces, with dysphasia and primitive reflexes, and eventually succumbed in a state of severe emaciation, generalized muscle wasting, and fasciculation, spontaneous or evoked by tapping.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationKuru plaques were found in about three quarters of the 13 cases of Beck and Daniel.
“in “about three quarters” of the 13 cases of Beck and Daniel (68)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [68] Beck E Daniel PM Kuru and scrapie compared: Are they examples of system degeneration? Gajdusek DC Gibbs CJ Jr Alpers MP Slow, Latent, and Temperate Virus Infections Washington, DC US Department of Health, Education, and Welfare 1965 85 93
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationFowler et al described severe demyelination in the lateral corticospinal tract and degeneration of dorsal and ventral spinocerebellar tracts in kuru.
“Fowler et al (67) described severe demyelination in the lateral corticospinal tract and degeneration of dorsal and ventral spinocerebellar tracts.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [67] Fowler M Robertson EG Observations on kuru. III. Pathological features in five cases Australas Ann Med 1959 8 16 26 13638205 source
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenKuru was divided into 3 clinical stages: ambulant, sedentary, and terminal.
“Kuru was divided into 3 clinical stages: ambulant, sedentary, and terminal.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationIntention tremor was detected in more than 50% of cases in Alpers' series in the first stage of kuru but was constantly present through the second stage.
“Intention tremor was detected in more than 50% of cases in Alpers’ series in the first stage of kuru but was constantly present through the second stage.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Alpers MP Kuru: A Clinical Study Washington, DC US Department of Health, Education, and Welfare 1964 1 38
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSwollen neurons are occasionally described in kuru.
“Swollen neurons were occasionally described (67, 68).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [67] Fowler M Robertson EG Observations on kuru. III. Pathological features in five cases Australas Ann Med 1959 8 16 26 13638205 source
- cites [68] Beck E Daniel PM Kuru and scrapie compared: Are they examples of system degeneration? Gajdusek DC Gibbs CJ Jr Alpers MP Slow, Latent, and Temperate Virus Infections Washington, DC US Department of Health, Education, and Welfare 1965 85 93
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationIn kuru, neurons are shrunken and either hyperchromatic or pale, with dispersion of the Nissl substance or intracytoplasmic vacuoles similar to those in scrapie.
“Neurons were shrunken and either hyperchromatic or pale, with dispersion of the Nissl substance or contained intracytoplasmic vacuoles similar to those that had been described in scrapie (66).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [66] Innes JRM Saunders LZ Comparative Neuropathology New York, NY Academic Press 1962 839
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBeck and Daniel noticed "small spongy spaces" in 7 of 13 kuru cases.
“but “small spongy spaces” were noticed in 7 of 13 cases studied by Beck and Daniel (68).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [68] Beck E Daniel PM Kuru and scrapie compared: Are they examples of system degeneration? Gajdusek DC Gibbs CJ Jr Alpers MP Slow, Latent, and Temperate Virus Infections Washington, DC US Department of Health, Education, and Welfare 1965 85 93
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationWell-documented accounts of the practice in Papua New Guinea have recently been published.
“well-documented accounts of the practice in Papua New Guinea have recently been published (54, 55).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [54] Knauft BM Good Company and Violence. Sorcery and Social Action in a Lowland New Guinea Society Berkeley, CA University of California Press 1985
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [55] Gillison G Between Culture and Fantasy A New Guinea Highlands Mythology Chicago, IL Chicago University Press 1993
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenSpongiform change is poorly visible in thick celloidin blocks stained with Nissl stain, as opposed to paraffin blocks stained with hematoxylin and eosin.
“It must be stressed, however, that the spongiform change is poorly visible in thick celloidin blocks stained with Nissl stain, as opposed to paraffin blocks stained with hematoxylin and eosin.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenThe discovery of transmissibility of kuru and subsequent transmission of CJD set the stage for the timely discovery of variant CJD almost 50 years later, without which its cause might have remained a mystery for a very long time.
“Also, the discovery of transmissibility of kuru and subsequent transmission of CJD would set the stage for the timely discovery of variant CJD almost 50 years later, without which its cause might have remained a mystery for a very long time.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenThe amount of ultrastructural data on kuru-affected brains is extremely limited, probably because of severe constraints on obtaining well-fixed material.
“The amount of ultrastructural data on kuru-affected brains is extremely limited probably because of severe constraints on obtaining well-fixed material.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationField et al. described a typical fine structure of amyloid plaques and numerous Hirano bodies in kuru brains.
“They described a typical fine structure of amyloid plaques as well as numerous Hirano bodies.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [81] Field EJ Mathews JD Raine CS Electron microscopic observations on the cerebellar cortex in kuru J Neurol Sci 1969 8 209 24 4185060 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationPeat and Field reported cytoplasmic lamellar bodies, which were subsequently shown to be normal cell constituents.
“Peat and Field (82) reported on “cytoplasmic lamellar bodies,” which subsequently were shown to be perfectly normal cell constituents (83).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAs early as 1969, Lampert et al. suggested that spongiform change is related to autophagy.
“It is of utmost interest that as early as 1969, Lampert et al (having cited an earlier article by Arstila et al [88]) suggested that the spongiform change is somehow related to autophagy (84).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [84] Lampert PW Earle KM Gibbs CJ Jr Experimental kuru encephalopathy in chimpanzees and spider monkey J Neuropathol Exp Neurol 1969 28 353 70 4978020 source
- cites [88] Arstila AU Trump BF Studies on cellular autophagocytosis. The formation of autophagic vacuoles in the liver after glucagon administration Am J Pathol 1968 53 687 733 4300890 PMC2013521
Probably not a substantial claim: may not pass S4 (based).
Premisenone givenKuru was the first slow virus disease of humans discovered in a remote tribe of Papua New Guinea.
“Kuru was the first slow virus disease of humans discovered in a remote tribe of Papua New Guinea.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Premisenone givenThe new type of human infectious pathogen called "a slow virus" was discovered through the work of D. Carleton Gajdusek and subsequent collaborators and followers.
“Through the insight, endurance, persistence, and genius of D. Carleton Gajdusek and subsequent collaborators and followers, the new type of human infectious pathogen, called “a slow virus,” was discovered.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based).
InterpretationreasoningThat discovery opened a new field of neurodegenerations viewed as protein conformational disorders.
“That discovery opened a new field of neurodegenerations viewed as protein conformational disorders.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationBeck et al. confirmed the pioneer data and reported membrane lamination observed before full-blown pathology could be appreciated.
“Those pioneer data were confirmed by Beck et al (89), who also reported membrane lamination observed before full-blown pathology could be appreciated.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [89] Beck E Bak IJ Christ JF Experimental kuru in the Spider monkey: Histopathological and ultrastructural studies of the brain during early stages of incubation Brain 1975 98 595 612 814967 source
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenThe histogenesis of vacuoles is not well understood, and most ultrastructural studies cannot detect the subcellular organelles from which vacuoles originate.
“The histogenesis of vacuoles is not well understood, and most of the ultrastructural studies have an inability to detect subcellular organelles from which vacuoles originate.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Premisenone givenWith the passage of time, the slow virus concept became a "prion."
“With the passage of time, the slow virus changed clothes to become a “prion.””
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataOur immunohistochemistry confirmed the presence of microglial cells, astrocytic processes, and dystrophic neurites at the periphery of kuru plaques and a striking resemblance of the amyloid plaques in kuru with those in the plaque subtype of sporadic CJD.
“Our immunohistochemistry confirmed the presence of microglial cells, astrocytic processes, and dystrophic neurites at the periphery of kuru plaques and a striking resemblance of the amyloid plaques in kuru with those in the plaque subtype of sporadic CJD.”
Quote in the paperSubstantial claim
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BackgroundUnconventional Viruses and the Origin and Disappearance of Kuru
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BackgroundResultExperimental Transmission of a Kuru-like Syndrome to Chimpanzees
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“In 1965, brain tissue from 3 kuru patients he had inoculated 2 years earlier transmitted the illness to chimpanzees (1, 12) and later to Rhesus monkeys (13), marmosets (14), and Gibbon and Sooty Mangabey monkeys (15).”
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BackgroundSelf-citationCreutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee
Gibbs, C. J., Gajdusek, D. C., Asher, D. M., Alpers, M. P., Beck, E., Daniel, P. M., & Matthews, W. B. (1968) · Science · doi:10.1126/science.161.3839.388 · Cited by 777 · see citing works
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“The methionine/valine (Met/ Val) variation at position 129 does not by itself cause the disease but dramatically influences the phenotype resulting from other PRNPmutations (23) and influences susceptibility/ resistance to kuru and iatrogenic and sporadic forms of CJD (24Y26).”
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“Kuru and Cannibalism When kuru was first reported as occurring in certain families and hamlets, confined to the Fore and adjacent people with whom they intermarried, and showing a predilection for young children and adult women (27), a genetic or hormonal explanation seemed to provide a key.”
BackgroundResultGenetic predisposition to iatrogenic Creutzfeldt-Jakob disease
Collinge, J., Palmer, M. S., & Dryden, A. J. (1991) · The Lancet · doi:10.1016/0140-6736(91)93128-v · Cited by 556 · cited 1× · see citing works
“Multiple mutations in the PRNP gene have been linked to various phenotypes of hereditary, sporadic, and iatrogenic CJD (25, 26).”
BackgroundCREUTZFELDT-JAKOB DISEASE VIRUS ISOLATIONS FROM THE GERSTMANN-STRÄUSSLER SYNDROME
Masters, C. L., Gajdusek, D. C., & Gibbs, C. J. (1981) · Brain · doi:10.1093/brain/104.3.559 · Cited by 527 · cited 1× · see citing works
“Indeed, GSS was transmitted to nonhuman primates in 1981 (74).”
BackgroundKuru in the 21st century—an acquired human prion disease with very long incubation periods
Collinge, J., Whitfield, J., McKintosh, E., Beck, J., Mead, S., Thomas, D. J., & Alpers, M. P. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68930-7 · Cited by 427 · see citing works
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Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics
Mead, S., Stumpf, M. P. H., Whitfield, J., Beck, J. A., Poulter, M., Campbell, T., Uphill, J. B., Goldstein, D., Alpers, M., Fisher, E. M. C., et al. (2003) · Science · doi:10.1126/science.1083320 · Cited by 394 · cited 2× · see citing works
“However, the exposure disappeared because of an Australian ‘‘carrot-and-stick’’ approach to the practice of cannibalism rather than by any biological or medical reason! Surprisingly, a balancing selection at the PRNP locus somewhat similar to what occurred in the Fore was discovered in some other world populations and…”
BackgroundLampert, P. W. (1967) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-196707000-00001 · Cited by 387 · cited 1× · see citing works
“Lampert, who had already published an article of degenerating neurites (85), also mentioned these structures that are now considered to be related to autophagy (86).”
BackgroundScrapie infectivity, fibrils and low molecular weight protein
Diringer, H., Gelderblom, H., Hilmert, H., Özel, M., Edelbluth, C., & Kimberlin, R. H. (1983) · Nature · doi:10.1038/306476a0 · Cited by 340 · cited 1× · see citing works
“This question remained open until the ‘‘protein-only’’ theory was formulated (18, 19), a protein that copurified with the infectivity was found (20), and S.”
Background(1968) · PubMed Central · Cited by 332 · see citing works
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Kuru Sorcery: Disease and Danger in the New Guinea Highlands
Lindenbaum, S. (1978) · Medical Entomology and Zoology · Cited by 231 · see citing works
Self-citationA Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure
Mead, S., Whitfield, J., Poulter, M., Shah, P., Uphill, J., Campbell, T., Al-Dujaily, H., Hummerich, H., Beck, J., Mein, C. A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0809716 · Cited by 206 · cited 2× · see citing works
“The loss of Met/Met genotype and accumulation of alternative alleles in the postepidemic Fore population was also indicated by the finding that the PRNP V127V synonymous substitution that showed the highest frequency in the surviving elderly women is part of the 127GGY129VV haplotype (38).”
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Sustainable agriculture and plant diseases: an epidemiological perspective
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Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt–Jakob disease
Cervenáková, L., Goldfarb, L. G., Garruto, R., Lee, H.-S., Gajdusek, D. C., & Brown, P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.22.13239 · Cited by 160 · cited 3× · see citing works
“This phenomenon was associated with increased susceptibility of the 129 Met/Met carriers who became early victims of the epidemic, disproportionally dying of the disease after the shortest incubation time (24, 37).”
BackgroundMethodSelf-citationGood Company and Violence: Sorcery and Social Action in a Lowland New Guinea Society
Valeri, V., & Knauft, B. M. (1987) · Journal for the Scientific Study of Religion · doi:10.2307/1385856 · Cited by 144 · see citing works
Increased Susceptibility to Kuru of Carriers of the <i>PRNP</i> 129 Methionine/Methionine Genotype
Lee, H., Brown, P., Cervenáková, L., Garruto, R. M., Alpers, M. P., Gajdusek, D. C., & Goldfarb, L. G. (2001) · The Journal of Infectious Diseases · doi:10.1086/317935 · Cited by 140 · cited 6× · see citing works
“The results of this analysis demonstrate that in the group of young Fore males just entering the age of risk, theMet/Met individuals were preferentially affected with kuru (37).”
BackgroundResultInfluentialSelf-citationStudies on cellular autophagocytosis
Arstila, A. U., Nuuja, I., & Trump, B. F. (1974) · Experimental Cell Research · doi:10.1016/0014-4827(74)90477-7 · Cited by 138 · see citing works
Liberski, P. P., Sikorska, B., Bratosiewicz-Wasik, J., Carleton Gajdusek, D., & Brown, P. (2004) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.04.016 · Cited by 125 · cited 1× · see citing works
“Thus, Lampert’s work preceded the current view that autophagy is one of the most important phenomena observed in all prion diseases (87, 88).”
BackgroundSelf-citationCollinge, J., Whitfield, J., McKintosh, E., Frosh, A., Mead, S., Hill, A. F., Brandner, S., Thomas, D., & Alpers, M. P. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0068 · Cited by 110 · see citing works
Electron microscopic observations on the cerebellar cortex in Kuru
Field, E. J., Mathews, J. D., & Raine, C. S. (1969) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(69)90111-7 · Cited by 89 · cited 1× · see citing works
“Field et al (81) used formalinfixed brains of 5 kuru cases to demonstrate degeneration of Purkinje cells, torpedo formation, and proliferation of Bergmann glia.”
MethodWadsworth, J. D. F., Joiner, S., Linehan, J. M., Desbruslais, M., Fox, K., Cooper, S., Cronier, S., Asante, E. A., Mead, S., Brandner, S., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800190105 · Cited by 89 · cited 3× · see citing works
“In contrast, inocula characterized by the type 2 PrP pattern change to the type 3 pattern on transmission (21).”
BackgroundArens, W. (1979) · Cited by 81 · see citing works
Pathology and Immunocytochemistry of a Kuru Brain
Hainfellner, J. A., Liberski, P. P., Guiroy, D. C., Cervénaková, L., Brown, P., Gajdusek, D. C., & Budka, H. (1997) · Brain Pathology · doi:10.1111/j.1750-3639.1997.tb01072.x · Cited by 78 · see citing works
Self-citationMathews, J., Glasse, R., & Lindenbaum, S. (1968) · The Lancet · doi:10.1016/s0140-6736(68)90482-0 · Cited by 74 · cited 2× · see citing works
“After the successful transmission by intracerebral inoculation of brain tissue homogenate in 1966 (1) and a publication proposing the cannibal connection (47), he presented his view more firmly that ‘‘even today, we have no evidence that eating bodies caused the spread.”
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EXPERIMENTAL KURU ENCEPHALOPATHY IN CHIMPANZEES AND SPIDER MONKEYS: ELECTRON— MICROSCOPIC STUDIES
LAMPERT, P. W., EARLE, K. M., GIBBS, C. J., & GAJDUSEK, D. C. (1969) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-196907000-00001 · Cited by 71 · see citing works
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“We were privileged to examine a case of a young male kuru patient named ‘‘K’’ from the South Fore region whose brain tissue had transmitted the disease to chimpanzees, and McLean et al (76, 77) examined a series of 11 cases of kuru.”
Self-citationGenetic susceptibility, evolution and the kuru epidemic
Mead, S., Whitfield, J. T., Poulter, M., Shah, P. R., Uphill, J. B., Beck, J. A., Campbell, T., Al-Dujaily, H., Hummerich, H., Alpers, M. P., et al. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0087 · Cited by 66 · cited 1× · see citing works
“Kuru is currently said to have exerted a strong selection pressure on the human PrP gene in the context of the Fore practice of endocannibalism (56).”
BackgroundKuru with incubation periods exceeding two decades
Prusiner, S. B., Gajdusek, D. C., & Alpers, M. P. (1982) · Annals of Neurology · doi:10.1002/ana.410120102 · Cited by 63 · see citing works
Between culture and fantasy: a New Guinea highlands mythology
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A possible genetic basis for kuru.
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NOBEL LECTURE: NMR Studies of Structure and Function of Biological Macromolecules
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NEUROPATHOLOGIC FINDINGS IN EXOTIC NEUROLOGIC DISORDERS AMONG NATIVES OF THE HIGHLANDS OF NEW GUINEA
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OBSERVATIONS ON KURU. III : PATHOLOGICAL FEATURES IN FIVE CASES
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“Fowler et al (67) described severe demyelination in the lateral corticospinal tract and degeneration of dorsal and ventral spinocerebellar tracts.”
BackgroundPROCEEDINGS OF THE AUSTRALIAN ASSOCIATION OF NEUROLOGISTS
Russell, W. R. (1969) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.32.1.69 · Cited by 39 · see citing works
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A clinico-pathological study of a case of kuru
Scrimgeour, E. M., Masters, C. L., Alpers, M. P., Kaven, J., & Gajusek, D. C. (1983) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(83)90044-8 · Cited by 37 · see citing works
Mortuary rites of the South Fore and kuru
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“A recent investigation of Fore mortuary practices has shown that, by consuming deceased relatives, the Fore were ensuring that the souls of the departed reached the land of the dead, to be reborn as ancestors (52).”
BackgroundGenetic studies in relation of kuru. I. Cultural, historical, and demographic background.
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Transmission of Kuru from Man to Rhesus Monkey (Macaca mulatta) 8½ Years after Inoculation
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Genetic Studies in Relation to Kuru: An Overview
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“DNA was recovered from frozen brain tissue, brain suspensions previously used in transmission studies, blood clots, serum samples, and other tissues stored in tissue banks (24, 36).”
MethodSelf-citationOBSERVATIONS ON KURU : I. A POSSIBLE GENETIC BASIS
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Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar?
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Self-citationThe neuropathology of kuru and variant Creutzfeldt–Jakob disease
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“We were privileged to examine a case of a young male kuru patient named ‘‘K’’ from the South Fore region whose brain tissue had transmitted the disease to chimpanzees, and McLean et al (76, 77) examined a series of 11 cases of kuru.”
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Transmission of Kuru and Creutzfeldt-Jakob Disease to Marmoset Monkeys
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Disease‐specific particles without prion protein in prion diseases – phenomenon or epiphenomenon?
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Self-citationAn unusual structure in Kuru brain
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“Field et al (81) used formalinfixed brains of 5 kuru cases to demonstrate degeneration of Purkinje cells, torpedo formation, and proliferation of Bergmann glia.”
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Prion genotypes in Central America suggest selection for the V129 allele
Hardy, J., Scholz, S., Evans, W., Goldfarb, L., & Singleton, A. (2006) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30248 · Cited by 7 · cited 1× · see citing works
“However, the exposure disappeared because of an Australian ‘‘carrot-and-stick’’ approach to the practice of cannibalism rather than by any biological or medical reason! Surprisingly, a balancing selection at the PRNP locus somewhat similar to what occurred in the Fore was discovered in some other world populations and…”
BackgroundSelf-citationFrontier Journeys. Fore Experiences on the Kuru Patrols.
Beasley, A. (2009) · Oceania · doi:10.1002/j.1834-4461.2009.tb00049.x · Cited by 6 · see citing works
Cerebellar lamellar bodies in two strains of murine scrapie
Liberski, P. P., & Gibson, P. H. (1987) · Journal of Comparative Pathology · doi:10.1016/0021-9975(87)90028-4 · Cited by 5 · cited 1× · see citing works
“Peat and Field (82) reported on ‘‘cytoplasmic lamellar bodies,’’ which subsequently were shown to be perfectly normal cell constituents (83).”
BackgroundSelf-citationWhitfield, J. T. (2011) · UCL Discovery (University College London) · Cited by 1 · see citing works
Flagged first, then by citations
Research works printed but not linked: 7
- Bennett, 1959, Am J Hum Genet, 11, 169
- Gajdusek, 1972, Am J Hum Gen, 24, 1
- Wiesenfeld, 1975, Am J Hum Gen, 27, 498
- Lindenbaum, 2009, Folia Neuropathol, 47, 138
- Klatzo, 1959, Lab Invest, 8, 799
- Seitelberger, 1962, Wien Klein Wochen, 74, 687
- Arstila, 1968, Am J Pathol, 53, 687
Cited by
Sorted by citations
Kuru, the First Human Prion Disease
Liberski, P. P., Gajos, A., Sikorska, B., & Lindenbaum, S. (2019) · Viruses · doi:10.3390/v11030232 · Cited by 69 · see citing works
Self-citationSporadic and Infectious Human Prion DiseasesPreprint
Will, R. G., & Ironside, J. W. (2016) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a024364 · Cited by 61 · see citing works
“Kuru occurred as an epidemic within the Fore tribe; its transmission was associated with ritualistic endocannibalism in the tribe, during which the brain was most often handled or consumed by women and children (Liberski et al. 2012).”
BackgroundMechanisms of prion-induced neurodegeneration
Saá, P., Harris, D. A., & Červen̆áková, L. (2016) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2016.8 · Cited by 50 · see citing works
Human Prion Diseases: From Kuru to Variant Creutzfeldt-Jakob Disease
Sikorska, B., & Liberski, P. P. (2012) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-5416-4_17 · Cited by 50 · see citing works
“to chimpanzee (Gajdusek 1977; Liberski et al. 2012).”
BackgroundSelf-citationHistorical overview of prion diseases: a view from afar.
Liberski, P. P. (2012) · PubMed · Cited by 49 · see citing works
Self-citationCharacteristics of Microbes Most Likely to Cause Pandemics and Global Catastrophes
Adalja, A. A., Watson, M., Toner, E. S., Cicero, A. J., & Inglesby, T. V. (2019) · Current topics in microbiology and immunology · doi:10.1007/82_2019_176 · Cited by 42 · see citing works
“Kuru, a geographically restricted prion disease, was spread via human cannibalism in Papua New Guinea, and the outbreak abated once that practice was ended in the 1960s (Liberski et al.”
BackgroundPrion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?
Ritchie, D. L., & Barria, M. A. (2021) · Biomolecules · doi:10.3390/biom11020207 · Cited by 39 · see citing works
Infectious prion diseases in humans: Cannibalism, iatrogenicity and zoonoses
Haı̈k, S., & Brandel, J. (2014) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2014.06.010 · Cited by 34 · see citing works
“The cardinal neuropathologic feature is the presence of amyloid plaques that are abundant notably in the granular cell layer of the cerebellum, the striatum, the thalami and the cerebral cortex (Liberski et al., 2012).”
BackgroundJankovská, N., Olejár, T., & Matěj, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010007 · Cited by 33 · see citing works
Kuru: A Journey Back in Time from Papua New Guinea to the Neanderthals’ Extinction
Liberski, P. P. (2013) · Pathogens · doi:10.3390/pathogens2030472 · Cited by 31 · see citing works
Self-citationDifferential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases
Lambert, Z. J., Greenlee, J. J., Cassmann, E. D., & Greenlee, M. H. W. (2021) · Viruses · doi:10.3390/v13122453 · Cited by 16 · see citing works
Emerging perspectives of copper-mediated transcriptional regulation in mammalian cell development
Fitisemanu, F. M., & Padilla‐Benavides, T. (2024) · Metallomics · doi:10.1093/mtomcs/mfae046 · Cited by 14 · see citing works
Spreading fun: Comic zombies, Joker viruses and COVID-19 jokes
Jürgens, A., Fiadotava, A., Tscharke, D. C., et al. (2021) · Journal of Science & Popular Culture · doi:10.1386/jspc_00024_1 · Cited by 14 · see citing works
Sun, X., Xu, Z., Wang, Y., et al. (2020) · Food Science and Human Wellness · doi:10.1016/j.fshw.2020.04.004 · Cited by 13 · see citing works
Prion, prionoids and infectious amyloid
Liberski, P. P. (2013) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(13)70021-x · Cited by 13 · see citing works
Self-citationDermatology Eponyms – sign –Lexicon (L)
Brzeziński, P., Chiriac, A. E., Arenas, R. G., et al. (2014) · Our Dermatology Online · doi:10.7241/ourd.20142.58 · Cited by 9 · see citing works
Tsou, A., Chen, P.-J., Tsai, K., Hu, W., & Lu, K. (2022) · Viruses · doi:10.3390/v14020408 · Cited by 9 · see citing works
Thellung, S., Gatta, E., Pellistri, F., Villa, V., Corsaro, A., Nizzari, M., Robello, M., & Florio, T. (2017) · Neurotoxicity Research · doi:10.1007/s12640-017-9749-2 · Cited by 8 · see citing works
Singer, A., Trigo, F. F., Vinel, L., et al. (2025) · The Journal of Physiology · doi:10.1113/jp285949 · Cited by 7 · see citing works
“Both Creutzfeldt–Jacob disease (Lafarga et al. 1993) and kuru (Liberski et al. 2012) were reported to go along with a conspicuous proliferation of FCs.”
Wısnıewskı, T., & Goñi, F. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63945-5.00023-4 · Cited by 6 · see citing works
Dermatology Eponyms – sign –Lexicon (K)
Brzeziński, P., Fiorentino, D. F., Arunachalam, P., et al. (2014) · Our Dermatology Online · doi:10.7241/ourd.20141.26 · Cited by 5 · see citing works
Liberski, P. P., & Ironside, J. W. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-398270-4.00023-9 · Cited by 5 · see citing works
Self-citationKuru Disease: Bridging the Gap Between Prion Biology and Human Health
Kothekar, H., & Chaudhary, K. (2024) · Cureus · doi:10.7759/cureus.51708 · Cited by 4 · see citing works
Pros and cons in prion diseases abatement: Insights from nanomedicine and transmissibility patterns
Chandrasekaran, M., Manivannan, P., & Muralitharan, G. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.12.150 · Cited by 3 · see citing works
Prionopathies and Prionlike Protein Aberrations in Neurodegenerative Diseases
Anderson, K. N., Overcast, W. B., Brosch, J. R., Graner, B. D., & Veronesi, M. C. (2021) · Neurographics · doi:10.3174/ng.2000035 · Cited by 1 · see citing works
The cannibalistic trade-off: Why human cannibalism emerges and why taboos suppress it
Misiak, M., & Tureček, P. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2605120123 · Cited by 1 · see citing works
Amyloidy i prionoidy – czy jest już czas, żeby się obawiać?
Liberski, P. P. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 1 · see citing works
Self-citationBelay, E. D., & Bartz, J. C. (2014) · Springer eBooks · doi:10.1007/978-1-4899-7448-8_47 · Cited by 1 · see citing works
Liberski, P. P., Ritchie, D. L., & Sikorska, B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85654-6.00004-6 · Cited by 1 · see citing works
Self-citationEnfermedades priónicas y enfermedades similares a priones
Juárez, J. C. C., Batres-Godoy, S. S., Calderón, M. J., Solís-Aguilar, R., Palencia, A. E., & Silva-Arévalo, G. (2022) · Neurología, Neurocirugía y Psiquiatría · doi:10.35366/108765 · Cited by 1 · see citing works
Liberski, P. P. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 1 · see citing works
Self-citationTwenty-year-old African American woman with prion disease associated with the G114V PRNP variant
Margolesky, J. H., & Saporta, M. (2018) · Neurology Genetics · doi:10.1212/nxg.0000000000000229 · Cited by 1 · see citing works
“It is interesting to note that such lability (including the inappropriate euphoria described early in her disease course) had been noted in Kuru, leading to the euphemisms “laughing disease” or “laughing death.(1)” Clonazepam was started to help with myoclonus, anxiety, and irritability.”
BackgroundRojas-Marcos, I., Díaz, L. F., Polo, R. Á., et al. (2014) · Elsevier eBooks · doi:10.1016/b978-84-9022-484-7.00016-1 · Cited by 1 · see citing works
Winter, G. (2015) · British Journal of Neuroscience Nursing · doi:10.12968/bjnn.2015.11.5.219
Kuru: Introduction to Prion Diseases
Liberski, P. P., & Gajos, A. (2017) · Neuromethods · doi:10.1007/978-1-4939-7211-1_1
Self-citationSorcery and Science: Honoring the Work of Shirley Lindenbaum
Gaines, A. D. (2017) · Culture Medicine and Psychiatry · doi:10.1007/s11013-017-9556-5
Sikorska, B., Gajos, A., Bogucki, A., Zielonka, E., Sigurdson, C. J., & Liberski, P. P. (2017) · Prion · doi:10.1080/19336896.2017.1384109
Self-citationAntemortem Diagnostics in Prion Disease
Gushue, D. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r34f1mv51
Ilman, A. (2021) · Archives in Neurology & Neuroscience · doi:10.33552/ann.2020.09.000717
“Random and unreasonable Laughing and brain working system complications [26] and Coma(in serious and final feature- not always happens) are the impacts on heal human body [27].”
BackgroundX-ray crystallographic fragment screening against the human prion protein
Rangel, V. L. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.60.2021.tde-27092021-150052
Belay, E. D., & Appleby, B. S. (2022) · Springer eBooks · doi:10.1007/978-1-4939-9544-8_47-1
Overview of human transmissible spongiform encephalopathies
Benavente, R., Catumbela, C. S. G., & Morales, R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-19130-5.00034-4
Prion Diseases of Animals and Humans
Steadman, B. S., & Bartz, J. C. (2024) · Springer eBooks · doi:10.1007/978-3-031-68237-7_29
Movement Disorders in Infectious Dementias
Cardoso, F., & Caramelli, P. (2014) · Springer eBooks · doi:10.1007/978-1-4471-6365-7_15
Thompson, A. G. B. (2014) · UCL Discovery (University College London)
A synthesis-based mapping of the landscape of neurodegenerative diseases
Winalai, C., & Bicout, D. (2026) · NeuroImage · doi:10.1016/j.neuroimage.2026.121700
Maladies neurodégénératives et stress oxydant
Lévy, E. (2020) · theses.fr (ABES) · doi:10.70675/75371581z194fz4cb4zb457z91bf72dc0320 · Cited by 4 · see citing works
Preclinical Models of Neurodegenerative Diseases
Cendelín, J., & Tuma, J. (2026) · Contemporary clinical neuroscience · doi:10.1007/978-3-032-18296-8_3
- Authors
- Liberski, P. P., Sikorska, B., Lindenbaum, S., Goldfarb, L. G., McLean, C., Hainfellner, J. A., & Brown, P.
- Affiliations
- Medical University of Lodz (PL)
- The Graduate Center, CUNY (US)
- National Institutes of Health (US)
- The Alfred Hospital (AU)
- University of Vienna (AT)
- Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR)
- Corresponding author
- Liberski, Pawel P.
- Venue
- Journal of Neuropathology & Experimental Neurology
- Publisher
- Oxford University Press (OUP)
- Published
- 2012-02
- Volume
- 71
- Issue
- 2
- Pages
- 92-103
- ISSN
- 0022-3069 (ISSN-L)
- PMC
- PMC5120877
- OpenAlex
- W2081414459
- Semantic Scholar
- d01baf15727a534490ed223183eef44688ef9ae1
- Cited by
- 50
- References
- 74
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 5 · 2022: 4 · 2021: 6 · 2020: 3 · 2019: 4 · 2018: 2 · 2017: 4 · 2016: 3 · 2015: 1 · 2014: 8 · 2013: 4 · 2012: 2
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuropathology & Experimental Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion)
- Funders
- Österreichische Agentur für Internationale Mobilität und Kooperation in Bildung, Wissenschaft und Forschung
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (ZIANS002973)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Prion Diseases and Protein Misfolding
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Amyloidosis: Diagnosis, Treatment, Outcomes
- Keywords
- kuru, prion disease, Fore people, cannibalism, balancing selection, cerebellar ataxia, choreiform movements, amyloid plaques, astrocyte proliferation, glial fibrillary acidic protein, Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker disease, variant Creutzfeldt-Jakob disease, experimental transmission
- MeSH terms
- Brain, Cannibalism, Glial Fibrillary Acidic Protein, Humans, Creutzfeldt-Jakob Syndrome, Kuru, Prions, Gerstmann-Straussler-Scheinker Disease
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-17.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-17.
Cited sources are checked by gpt-6-sol.
Statistics and arithmetic are recomputed, not judged.
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