The DOI matches its Crossref record; 66 of the 66 references it cites were found in a registry or an index; 27 of the 65 sources its claims cite were checked for support.
National Institute on Aging–Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach
Open accessAbstract
We present a practical guide for the implementation of recently revised National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease (AD). Major revisions from previous consensus criteria are: (1) recognition that AD neuropathologic changes may occur in the apparent absence of cognitive impairment, (2) an "ABC" score for AD neuropathologic change that incorporates histopathologic assessments of amyloid β deposits (A), staging of neurofibrillary tangles (B), and scoring of neuritic plaques (C), and (3) more detailed approaches for assessing commonly co-morbid conditions such as Lewy body disease, vascular brain injury, hippocampal sclerosis, and TAR DNA binding protein (TDP)-43 immunoreactive inclusions. Recommendations also are made for the minimum sampling of brain, preferred staining methods with acceptable alternatives, reporting of results, and clinico-pathologic correlations.
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11 No full text of the sources · 9 Partly supported · 4 Supported · 3 Supported so far · 1 Own interpretation · accuracy not yet measured
Every source the paper cites for this claim was checked and supports it.
In the paper
“recognition that AD neuropathologic changes may occur in the apparent absence of cognitive impairment”
- Also stated in: § CLINICO-PATHOLOGIC CORRELATION · plain
“Similar neuropathologic changes, albeit usually at lower levels, also occur in individuals who did not show cognitive or behavioral impairments during life [54].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > Abstract
What the sources say
- Supportedcites [54] Sperling RA, Aisen PS, Beckett LA et al (2011) Toward defining the preclinical stages of Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement 7:280–292 source
Section 6 reports that AD-related biomarker abnormalities can be detected before overt clinical symptoms and that Aβ accumulation occurs in clinically normal older adults. Section 2 also notes that some people have diagnostic AD neuropathological features at autopsy without having developed dementia during life. No page numbers are available in our copy. (LLM, conf=0.94)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § CLINICO-PATHOLOGIC CORRELATION · plain
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“LBs may be detected in neurons of medulla, pons and midbrain with hematoxylin and eosin (H&E)-stained sections; however, greater sensitivity can be achieved with immunohistochemistry for α-synuclein and this approach is strongly preferred [3,4,13].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > LEWY BODY DISEASE > Method
What the sources say
- Partly supportedcites [3] Alafuzoff I, Parkkinen L, Al-Sarraj S et al (2008) Assessment of alpha-synuclein pathology: a study of the BrainNet Europe Consortium. J Neuropathol Exp Neurol 67:125–143 sourceExperimental — accuracy not yet measured
The Introduction (p. 125) says consensus guidelines recommend α-synuclein immunohistochemistry for synucleinopathies, supporting the preference for that approach. The paper’s staining results and Discussion assess variation among immunohistochemical methods, but do not establish that immunohistochemistry detects Lewy bodies more sensitively than H&E; searches for H&E and hematoxylin–eosin found no such comparison. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites [4] Alafuzoff I, Pikkarainen M, Al-Sarraj S et al (2006) Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium. J Neuropathol Exp Neurol 65:740–757 source
- Partly supportedcites [13] Beach TG, White CL, Hamilton RL et al (2008) Evaluation of alpha-synuclein immunohistochemical methods used by invited experts. Acta Neuropathol 116:277–288 sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) calls α-synuclein immunohistochemistry the method of choice for diagnosing Lewy body disorders, supporting its preferred use. The paper compares immunohistochemical methods with one another, however, and does not establish that they detect Lewy bodies more sensitively than H&E staining. (LLM, conf=0.84)
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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- Partly supported
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In the paper
“one MVL identified in standard sections of brain (Table 1 regions shaded green) is of unclear relationship to cognitive function, while multiple MVLs in these regions are associated with increased likelihood of cognitive impairment or dementia [24,52,62].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > CEREBROVASCULAR DISEASE and VASCULAR BRAIN INJURY > Reporting
What the sources say
- Partly supportedcites [24] Gorelick PB, Scuteri A, Black SE et al (2011) Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 42:2672–2713 sourceExperimental — accuracy not yet measured
Section 3.2 (page not available in our copy) reports that some studies associate multiple microscopic infarcts with dementia, even after accounting for macroscopic infarcts. It does not establish the claim for MVLs generally or specify that the lesions were identified in standard brain sections. (LLM, conf=0.82)
- Not checked — no full text of the sourcecites [52] Sonnen JA, Larson EB, Crane PK et al (2007) Pathological correlates of dementia in a longitudinal, population-based sample of aging. Ann Neurol 62:406–413 source
- Not checked — no full text of the sourcecites [62] White L (2009) Brain lesions at autopsy in older Japanese-American men as related to cognitive impairment and dementia in the final years of life: a summary report from the Honolulu-Asia aging study. J Alzheimers Dis 18:713–725 source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Clinico-pathologic correlations for individuals without cognitive impairment should indicate that it is possible for AD neuropathologic change to predate onset of symptoms by years [54].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > AD NEUROPATHOLOGIC CHANGE > Reporting
What the sources say
- Supportedcites [54] Sperling RA, Aisen PS, Beckett LA et al (2011) Toward defining the preclinical stages of Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement 7:280–292 source
Section 2, “Redefining the earliest stages of AD,” says the pathological cascade may begin a decade or more before clinically evident impairment. Section 6 also describes AD-related abnormalities in cognitively normal individuals, supporting the claim that neuropathologic change can predate symptoms by years. (LLM, conf=0.94)
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“one MVL identified in standard sections of brain (Table 1 regions shaded green) is of unclear relationship to cognitive function, while multiple MVLs in these regions are associated with increased likelihood of cognitive impairment or dementia [24,52,62].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > CEREBROVASCULAR DISEASE and VASCULAR BRAIN INJURY > Reporting
What the sources say
- Partly supportedcites [24] Gorelick PB, Scuteri A, Black SE et al (2011) Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 42:2672–2713 sourceExperimental — accuracy not yet measured
Section 3.2 (page unavailable) says the number of infarcts needed for cognitive impairment is difficult to determine and reports that multiple microscopic infarcts may be related to dementia. It does not specifically assess the cognitive significance of one MVL identified in standard brain sections. (LLM, conf=0.82)
- Not checked — no full text of the sourcecites [52] Sonnen JA, Larson EB, Crane PK et al (2007) Pathological correlates of dementia in a longitudinal, population-based sample of aging. Ann Neurol 62:406–413 source
- Not checked — no full text of the sourcecites [62] White L (2009) Brain lesions at autopsy in older Japanese-American men as related to cognitive impairment and dementia in the final years of life: a summary report from the Honolulu-Asia aging study. J Alzheimers Dis 18:713–725 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“this may represent pre-clinical LBD [12,22,31].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > LEWY BODY DISEASE > Reporting
What the sources say
- Supportedcites [12] Beach TG, Adler CH, Sue LI et al (2008) Reduced striatal tyrosine hydroxylase in incidental Lewy body disease. Acta Neuropathol 115:445–451 source
The Introduction defines incidental Lewy body disease as Lewy bodies without clinically documented parkinsonism or dementia. The Results and discussion report reduced striatal tyrosine hydroxylase in these individuals and say this suggests ILBD is likely a precursor to Parkinson’s disease and/or dementia with Lewy bodies, supporting the citing sentence’s qualified “may represent” claim. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites [22] Dickson DW, Fujishiro H, DelleDonne A et al (2008) Evidence that incidental Lewy body disease is pre-symptomatic Parkinson’s disease. Acta Neuropathol 115:437–444 source
- Supportedcites [31] Jicha GA, Schmitt FA, Abner E et al (2010) Prodromal clinical manifestations of neuropathologically confirmed Lewy body disease. Neurobiol Aging 31:1805–1813 source
The Introduction (page unavailable) says Lewy body pathology has been found in autopsied people described as normal and suggests that DLB pathology may predate clinical diagnosis. The Discussion (page unavailable) also says the study’s subjects were cognitively and neurologically normal at enrollment. Together, these support the qualified suggestion that LBD without apparent cognitive or motor deficits may be pre-clinical. (LLM, conf=0.91)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“LBs are frequent in the setting of moderate-to-severe levels of AD neuropathologic change [27,59], including some early-onset familial AD cases [32,33].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > LEWY BODY DISEASE
What the sources say
- Supportedcites [32] Leverenz JB, Fishel MA, Peskind ER et al (2006) Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype. Arch Neurol 63:370–376 source
The Results report Lewy body pathology in the amygdala of 24 of 25 familial AD cases with PSEN1 mutations. The section on PSEN1-associated AD reports a mean age at onset of about 43 years in the groups it compares, supporting the early-onset qualifier. The indexed copy provides section labels but no page numbers. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites [33] Lippa CF, Duda JE, Grossman M et al (2007) DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Neurology 68:812–819 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Accumulation of Aβ plaques and NFTs follows distinct regional progressions across brain regions as AD advances.”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > AD NEUROPATHOLOGIC CHANGE
What the sources say
- Partly supportedcites [14] Braak H, Alafuzoff I, Arzberger T et al (2006) Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry. Acta Neuropathol 112:389–404 sourceExperimental — accuracy not yet measured
The staging-system section describes a predictable regional progression of neurofibrillary pathology, from transentorhinal and entorhinal regions to limbic and then neocortical areas. It does not describe a separate regional progression of Aβ plaques or compare that progression with NFTs. Its references to neuritic plaques occur in the context of tau-immunoreactive pathology, not an Aβ-plaque staging scheme. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [15] Braak H, Braak E (1991) Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82:239–259 source
- Not checked — no full text of the sourcecites [57] Thal DR, Rub U, Orantes M, Braak H (2002) Phases of A beta-deposition in the human brain and its relevance for the development of AD. Neurology 58:1791–1800 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“CVD and vascular brain injury (VBI) [50] commonly are encountered in the brains with AD neuropathologic change [25].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > CEREBROVASCULAR DISEASE and VASCULAR BRAIN INJURY
What the sources say
- Partly supportedcites [25] Grinberg LT, Thal DR (2010) Vascular pathology in the aged human brain. Acta Neuropathol 119:277–290 sourceExperimental — accuracy not yet measured
The ‘Cerebral amyloid angiopathy’ section (page unavailable) reports that around 80–100% of AD patients have CAA, supporting the claim that cerebrovascular disease commonly accompanies AD pathology. It identifies infarction and hemorrhage as possible complications of CAA, but does not establish that vascular brain injury itself is commonly found in AD brains. (LLM, conf=0.82)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“LBs are frequent in the setting of moderate-to-severe levels of AD neuropathologic change [27,59], including some early-onset familial AD cases [32,33].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > LEWY BODY DISEASE
What the sources say
- Not checked — no full text of the sourcecites [27] Hamilton RL (2000) Lewy bodies in Alzheimer’s disease: a neuropathological review of 145 cases using alpha-synuclein immunohistochemistry. Brain Pathol 10:378–384 source
- Supportedcites [59] Uchikado H, Lin WL, DeLucia MW, Dickson DW (2006) Alzheimer disease with amygdala Lewy bodies: a distinct form of alpha-synucleinopathy. J Neuropathol Exp Neurol 65:685–697 source
The Materials and Methods section (page unavailable) says all 347 cases met pathologic criteria for AD and had Braak NFT stage IV or greater, indicating advanced AD in almost all cases. The “Frequency of α-Synuclein Pathology in Alzheimer Disease” section (page unavailable) reports Lewy-body pathology in 62 AD/ALB and 149 AD/LBD cases, supporting that Lewy bodies are frequent in this setting. (LLM, conf=0.90)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 2
- Probably not a substantial claim. 1
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Relatively isolated HS may occur in very old individuals, and in this context it is associated with TDP-43-immunoreactive inclusions and with cognitive impairment [45,47].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > HIPPOCAMPAL SCLEROSIS and TAR DNA BINDING PROTEIN (TDP)-43 INCLUSIONS > Reporting
What the sources say
- Partly supportedcites [45] Nelson PT, Abner EL, Schmitt FA et al (2010) Modeling the association between 43 different clinical and pathological variables and the severity of cognitive impairment in a large autopsy cohort of elderly persons. Brain Pathol 20:66–79 sourceExperimental — accuracy not yet measured
The Discussion reports that hippocampal sclerosis (HS) was associated with lower MMSE scores and states that HS is associated with TDP-43 proteinopathy. The Results describe TDP-43-positive inclusions. Neither passage establishes these associations specifically for relatively isolated HS in very old individuals. (LLM, conf=0.86)
- Supportedcites [47] Nelson PT, Schmitt FA, Lin Y et al (2011) Hippocampal sclerosis in advanced age: clinical and pathological features. Brain 134:1506–1518 source
The Introduction describes hippocampal sclerosis in older individuals as unrelated to Alzheimer’s pathology and associated with significant cognitive dysfunction. The Discussion reports aberrant TDP-43 staining in approximately 90% of patients with hippocampal sclerosis, and Table 7 describes HS-Ageing as most prevalent in the oldest-old and associated with dementia. The association is not universal, but the citing sentence does not claim that it is. (LLM, conf=0.92)
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
In the paper
“Although not part of this classification scheme, it is important to realize that LBD also occurs frequently in the olfactory bulb in older adults and should be sampled when possible [20].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > LEWY BODY DISEASE > Method
What the sources say
- Not checked — no full text of the sourcecites [20] Del Tredici K, Rub U, De Vos RA et al (2002) Where does Parkinson disease pathology begin in the brain? J Neuropathol Exp Neurol 61:413–426 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“A subset of senile plaques called neuritic plaques appear closely associated with neuronal injury and are characterized by the occurrence of dystrophic neurites that frequently have phospho-tau immunoreactivity [19,36,37,55].”
§ National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach > AD NEUROPATHOLOGIC CHANGE
What the sources say
- Not checked — no full text of the sourcecites [19] DeKosky ST, Scheff SW (1990) Synapse loss in frontal cortex biopsies in Alzheimer’s disease: correlation with cognitive severity. Ann Neurol 27:457–464 source
- Not checked — no full text of the sourcecites [36] Masliah E, Mallory M, Deerinck T et al (1993) Re-evaluation of the structural organization of neuritic plaques in Alzheimer’s disease. J Neuropathol Exp Neurol 52:619–632 source
- Not checked — no full text of the sourcecites [37] Masliah E, Terry RD, Mallory M et al (1990) Diffuse plaques do not accentuate synapse loss in Alzheimer’s disease. Am J Pathol 137:1293–1297
- Not checked — no full text of the sourcecites [55] Terry RD, Masliah E, Salmon DP et al (1991) Physical basis of cognitive alterations in Alzheimer’s disease: synapse loss is the major correlate of cognitive impairment. Ann Neurol 30:572–580 source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper relies on this without support.
Many other neurodegenerative disorders can cause dementia and may be co-morbid with AD neuropathologic change, especially in the elderly.
“There are many other neurodegenerative disorders that can cause dementia in addition to those discussed here, and any may be co-morbid with AD neuropathologic change, especially in the elderly.”
The paper relies on this without support.
Multiple diseases in the cerebrum can conspire to worsen cognitive symptoms.
“Multiple diseases in cerebrum can conspire to worsen cognitive symptoms; however, it often is difficult to judge the extent to which each disease observed at autopsy may have contributed to a given patient’s cognitive state.”
The paper relies on this without support.
Abnormal neuropil and neuronal cytoplasmic α-synuclein immunoreactivity are usually present with Lewy bodies but will not be apparent by H&E; in some instances, these changes occur in the absence of Lewy bodies.
“Abnormal neuropil and neuronal cytoplasmic α-synuclein immunoreactivity are usually present with LBs but will not be apparent by H&E; in some instances, these changes occur in the absence of LBs.”
The paper relies on this without support.
Diffuse white matter injury is a form of VBI but it is more difficult to judge objectively and is not specific to VBI.
“Diffuse white matter injury is a form of VBI but it is more difficult to judge objectively and is not specific to VBI.”
The paper relies on this without support.
Hippocampal sclerosis can be observed in the context of AD neuropathologic change, FTLD, and VBI, likely reflecting a heterogeneous etiology.
“HS can be observed in the context of AD neuropathologic change, frontotemporal lobar degeneration (FTLD), and VBI, likely reflecting a heterogeneous etiology.”
The paper relies on this without support.
Hippocampal sclerosis can be focal, so its absence in the recommended screening section does not rule out the possibility of HS elsewhere in the hippocampal formation.
“HS can be focal, thus its absence in the recommended screening section does not rule out the possibility of HS elsewhere in the hippocampal formation.”
The paper relies on this without support.
Hippocampal sclerosis can occur in several different diseases and has varying clinical implications in different settings.
“Clinico-pathological correlations need to recognize that HS can occur in several different diseases and has varying clinical implications in different settings.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The new NIA criteria use the same combination of NPs and Braak stage as the minimum lesion density necessary for attributing the cause of dementia to AD (39, 40).”
From Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005–2010 (2012) · cites this paper as [40]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The definitive diagnosis of AD requires microscopic examination of multiple brain regions employing staining methods that can detect Alzheimer type neuropathologic change [24], with diagnosis based upon the morphology and density of lesions and their topographic distribution.”
From The neuropathological diagnosis of Alzheimer's disease (2019) · cites this paper as [24]
The cited source says what the claim attributes to it.
In the citing paper
“This finding is highlighted by the fact that nearly one third of patients with pathological findings of high likelihood Alzheimer’s disease [24] were thought to other disorders, and 3% were considered clinically normal at the time of their last clinical exam (Table 2).”
From The neuropathological diagnosis of Alzheimer's disease (2019) · cites this paper as [24]
The cited source says what the claim attributes to it.
In the citing paper
“However, both Aβ and paired helical filament (PHF) tau deposits are required to fulfill neuropathologic criteria for AD [105,106]”
From NIA‐AA Research Framework: Toward a biological definition of Alzheimer's disease (2018) · cites this paper as [105]
The cited source says what the claim attributes to it.
In the citing paper
“Autopsy analyses classified the level of ADNC from “none” to “high” using an established scoring system when available.”
From Automatic classification of AD pathology in FTD phenotypes using natural speech (2024) · cites this paper as [30]
The cited source says what the claim attributes to it.
In the citing paper
“Participants in the Confirmed-AD group (n ¼ 1854) were diagnosed with primary or contributing ADdementia at their last UDS visit before death and met our criteria for ADNC: moderate to frequent neuritic plaques and Braak stages III through VI, which loosely aligns with NIA-AA criteria for intermediate or high ADNC (13).”
From Concordance of Clinical Alzheimer Diagnosis and Neuropathological Features at Autopsy (2020) · cites this paper as [13]
The cited source says what the claim attributes to it.
In the citing paper
“The shortcomings of the NIA-Reagan criteria have been recognized and a revised set of criteria are currently in press (39, 40).”
From Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005–2010 (2012) · cites this paper as [40]
The cited source says what the claim attributes to it.
In the citing paper
“In the revision of the 1997 criteria, combinations of plaque and tangle pathologies considered sufficient to cause dementia and qualify for the neuropathological diagnosis of AD are explicitly stated (40, 41).”
From Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005–2010 (2012) · cites this paper as [40]
The cited source says what the claim attributes to it.
In the citing paper
“Neuropathologic diagnosis of AD was in accordance with current NIA-AA guidelines (Hyman et al., 2012; Montine et al., 2012).”
From Cholesterol and matrisome pathways dysregulated in astrocytes and microglia (2022) · cites this paper as Montine et al., 2012
In the citing paper
“Neuropathological assessment was performed by 2 authors (T.G.B. and T.J.M.) blinded to clinical and imaging results and using NIA–AA diagnostic scoring guidelines.5,40”
From Positron Emission Tomography Imaging With [ 18 F]flortaucipir and Postmortem Assessment of Alzheimer Disease Neuropathologic Changes (2020) · cites this paper as [40]
In the citing paper
“Additional changes that may also occur in the brains of AD patients include amyloid angiopathy, age-related brain atrophy, synaptic pathology, white matter rarefaction, granulovacuolar degeneration, neuron loss, TDP-43 proteinopathy, and neuroinflammation (20-26), which may contribute to cognitive impairment; however, these are not considered pathognomonic features of AD (3).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [3]
In the citing paper
“In contrast, dense and extensive neocortical NFTs are very consistently associated with dementia and thus, according to new diagnostic criteria, these are required to constitute high burden of AD neuropathologic change (3).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [3]
In the citing paper
“The current revision of the National Institute on Aging–Alzheimer’s Association guidelines for the neuropathologic assessment of AD stipulate that subjects with moderately dense neuritic AβPs may be regarded as having an intermediate level of AD neuropathologic change and that other potential contributors to cognitive impairment and dementia should be sought (3).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [3]
In the citing paper
“There is no universally applied rubric for CVD pathologic diagnosis, although the recent National Institute on Aging–Alzheimer’s Association criteria attempted to systematize neuropathologic assessment of this complex form of brain injury (3).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [3]
In the citing paper
“Alzheimer's disease cases met criteria for a high likelihood of AD (Montine et al., 2012).”
From Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue (2020) · cites this paper as Montine et al., 2012
Citations
Cites
McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack, C. R., Kawas, C. H., Klunk, W. E., Koroshetz, W. J., Manly, J. J., Mayeux, R., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.005 · Cited by 18,657 · cited 1×
“‘‘Alzheimer’s disease’’ refers to a constellation of cognitive and behavioral changes that are typical for patients who have substantial amounts of its hallmark lesions [6, 39].”
Self-citationNeuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123 · cited 8×
“‘‘Intermediate’’ or ‘‘High’’ AD neuropathologic change (italicized) is considered sufficient explanation for dementia a NFT stage should be determined by the method of Braak [14, 15] b Ab/amyloid plaque score should be determined by the method of Thal et al.”
InfluentialStaging of brain pathology related to sporadic Parkinson’s disease
Braak, H., Tredici, K. D., Rüb, U., de Vos, R. A. I., Jansen Steur, E. N. H., & Braak, E. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00065-9 · Cited by 10,777 · cited 2×
“Given our focus on cognitive impairment and dementia rather than movement disorders [16], we recommend a modification of Fig.”
Albert, M. S., DeKosky, S. T., Dickson, D., Dubois, B., Feldman, H. H., Fox, N. C., Gamst, A., Holtzman, D. M., Jagust, W. J., Petersen, R. C., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.008 · Cited by 10,152 · cited 1×
“‘‘Alzheimer’s disease’’ refers to a constellation of cognitive and behavioral changes that are typical for patients who have substantial amounts of its hallmark lesions [6, 39].”
Self-citationSperling, R. A., Aisen, P. S., Beckett, L. A., Bennett, D. A., Craft, S., Fagan, A. M., Iwatsubo, T., Jack, C. R., Kaye, J., Montine, T. J., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.003 · Cited by 7,155 · cited 2×
“Similar neuropathologic changes, albeit usually at lower levels, also occur in individuals who did not show cognitive or behavioral impairments during life [54].”
Self-citationDiagnosis and management of dementia with Lewy bodies: Third report of the DLB consortium
McKeith, I. G., Dickson, D. W., Lowe, J., Emre, M., O'Brien, J. T., Feldman, H., Cummings, J., Duda, J. E., Lippa, C., Perry, E. K., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000187889.17253.b1 · Cited by 5,069
Self-citationMirra, S. S., Heyman, A., McKeel, D., Sumi, S. M., Crain, B. J., Brownlee, L. M., Vogel, F. S., Hughes, J. P., Belle, G. V., Berg, L., et al. (1991) · Neurology · doi:10.1212/wnl.41.4.479 · Cited by 4,961 · cited 11×
“Region Stain for A /amyloid plaques [57] Stain for NFTs [14,15] Stain for NPs [41] Stain for LBs H&E”
InfluentialSelf-citationDeJesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., Nicholson, A. M., Finch, N. A., Flynn, H., Adamson, J., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.011 · Cited by 4,936 · cited 1×
“With the exception of individuals with mutations in TARDBP, GRN, VCP or c9ORF72 [10, 18], it is not clear whether TDP-43 proteinopathy in these other neurodegenerative diseases is”
Self-citationTerry, R. D., Masliah, E., Salmon, D. P., Butters, N., DeTeresa, R., Hill, R., Hansen, L. A., & Katzman, R. (1991) · Annals of Neurology · doi:10.1002/ana.410300410 · Cited by 4,397 · cited 1×
“frequently have phospho-tau immunoreactivity [19, 36, 37, 55].”
Self-citationGorelick, P. B., Scuteri, A., Black, S. E., DeCarli, C., Greenberg, S. M., Iadecola, C., Launer, L. J., Laurent, S., Lopez, O. L., Nyenhuis, D., et al. (2011) · Stroke · doi:10.1161/str.0b013e3182299496 · Cited by 3,811
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Sorted by citations
Items 1,601–1,700 of 2,854
Sakurai, K., Iwase, T., Kaneda, D., Uchida, Y., Inui, S., Morimoto, S., Kimura, Y., Kato, T., Nihashi, T., Ito, K., et al. (2021) · Journal of Alzheimer's Disease · doi:10.3233/jad-210638 · Cited by 12
“…were selected by applying the following inclusion criteria: 1) neuropathological diagnoses according to the published criteria of AD and AGD [12, 13], 2) dementia status according to the major neurocognitivedisordersoftheDiagnosticandStatis-ticalManualofMentalDisorders(DSM)-Vcriteria,…”
Co-expression network analysis of frontal cortex during the progression of Alzheimer’s disease
Beck, J. S., Madaj, Z., Cheema, C. T., Kara, B., Bennett, D. A., Schneider, J. A., Gordon, M. N., Ginsberg, S. D., Mufson, E. J., & Counts, S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac001 · Cited by 12
Self-citationPhases of volume loss in patients with known frontotemporal lobar degeneration spectrum pathology
Burke, S., Phillips, J. S., Olm, C. A., Peterson, C. S., Cook, P. A., Gee, J. C., Lee, E. B., Trojanowski, J. Q., Massimo, L. M., Irwin, D. J., et al. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2022.02.007 · Cited by 12
Self-citationDivergent Histopathological Networks of Frontotemporal Degeneration Proteinopathy Subytpes
Chen, M., Ohm, D. T., Phillips, J. S., McMillan, C. T., Capp, N., Peterson, C., Xie, E., Wolk, D. A., Trojanowski, J. Q., Lee, E. B., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.2061-21.2022 · Cited by 11
Self-citationNeuropathological Insights into Unexpected Cognitive Decline in Epilepsy
Reimers, A., Helmstaedter, C., Elger, C. E., Pitsch, J., Hamed, M., Becker, A. J., & Witt, J. (2022) · Annals of Neurology · doi:10.1002/ana.26557 · Cited by 12
“In contrast, all patients (3 of 3 patients) with frontal resections revealed Aβ-associated deposits; that is, at an anatomical site where Aβ deposits are often primarily observed in Alzheimer disease (AD).(77) Intriguingly, both alterations, AT8-positive neurofibrillary tangles and Aβ plaques, were present adjacent to…”
ResultChourrout, M., Sandt, C., Weitkamp, T., Dučić, T., Meyronet, D., Baron, T., Klohs, J., Rama, N., Boutin, H., Singh, S., et al. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2023.07.046 · Cited by 12
Multiple system atrophy with amyloid-β-predominant Alzheimer’s disease neuropathologic change
Kon, T., Ichimata, S., Luca, D. G. D., Martínez-Valbuena, I., Kim, A., Yoshida, K., Alruwaita, A. A., Kleiner, G., Strafella, A. P., Forrest, S. L., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae141 · Cited by 13
“9 Additionally, the types of cerebral amyloid angiopathy (CAA), 20 Lewy, 21 TDP-43 22 and vascular pathologies 21,22 including arteriolo-sclerosis, infarcts and haemorrhages were evaluated.”
Hunter, S., Minett, T., Polvikoski, T. M., Mukaetova‐Ladinska, E. B., & Brayne, C. (2015) · Alzheimer s Research & Therapy · doi:10.1186/s13195-015-0141-2 · Cited by 12
Giaccone, G. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150435 · Cited by 12
“ISSN 1387-2877/15/$35.00 © 2015 – IOS Press have proposed a probabilistic view aimed to establish the likelihood that a certain level of AD pathology is responsible for or associated with dementia [1]. morphologically and antigenically identical to that found in AD but lacking A (cid:1) deposition are relatively frequ…”
InfluentialChilumuri, A., Ashioti, M., Nercessian, A. N., & Milton, N. G. N. (2013) · Journal of Neurodegenerative Diseases · doi:10.1155/2013/879710 · Cited by 12
“Hindawi Publishing Corporation Journal of Neurodegenerative Diseases Volume 2013, Article ID 879710, 11 pages http://dx.doi.org/10.1155/2013/879710”
BackgroundInfluentialMiki, T., Yokota, O., Ishizu, H., et al. (2016) · Neuropathology · doi:10.1111/neup.12290 · Cited by 12
Neuropathologic Associations of Learning and Memory in Primary Progressive Aphasia
Kielb, S. J., Cook, A., Wieneke, C. A., Rademaker, A., Bigio, E., Mesulam, M., Rogalski, E., & Weintraub, S. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.0880 · Cited by 14
Self-citationBarrick, B. J., Ida, C. M., Laniosz, V., et al. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.06.015 · Cited by 12
Bharadwaj, R., Cimino, P. J., Flanagan, M. E., Latimer, C. S., Gonzalez‐Cuyar, L. F., Juric‐Sekhar, G., Montine, T. J., Marshall, D. A., & Keene, C. D. (2017) · Histopathology · doi:10.1111/his.13345 · Cited by 12
“related disorders.(1,2) The guidelines recommend sampling 20 separate brain regions using diverse histochemical and/or immunohistochemical stains to characterise AD pathology according to amyloid plaque(3) and neurofibrillary tangle(4) distribution, neuritic plaque density(5) and other disease processes, including cer…”
BackgroundSelf-citationMorgello, S., Jacobs, M. M., Murray, J., Byrd, D., Neibart, E., Mintz, L., Meloni, G., Chon, C., & Crary, J. F. (2018) · Journal of NeuroVirology · doi:10.1007/s13365-018-0663-z · Cited by 13
Coomans, C., Sieben, A., Lammens, M. M. Y., Groote, C. C., Vandenbroecke, C., Goethals, I., Melkebeke, D. V., & Hemelsoet, D. (2018) · Acta Neurologica Belgica · doi:10.1007/s13760-018-1023-8 · Cited by 12
Autopsy case of V180I genetic Creutzfeldt‐Jakob disease presenting with early disease pathology
Iwasaki, Y., Kato, H., Ando, T., et al. (2018) · Neuropathology · doi:10.1111/neup.12516 · Cited by 12
“Therefore, the ABC scores for the neuropathologic changes in AD were (amyloid-β stain) A3, (NFT stain) B2, and (neuritic plaque stain) C3, respectively.(16) A mild cerebral amyloid angiopathy was observed.”
BackgroundLee, C. S., Study, F. T. A. C. I. T. (., Larson, E. B., Gibbons, L. E., Latimer, C. S., Rose, S. E., Hellstern, L. L., Keene, C. D., & Crane, P. K. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181087 · Cited by 12
Relationship Between Tau, β Amyloid and α-Synuclein Pathologies
Walker, L., & Attems, J. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9358-8_14 · Cited by 12
Zhang, W., Zhang, Q., Yang, Q., Liu, P., Sun, T., Xu, Y., Qian, X., Qiu, W., & Ma, C. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.02.022 · Cited by 12
Gollan, T. H., Smirnov, D. S., Salmon, D. P., & Galasko, D. (2020) · Psychology and Aging · doi:10.1037/pag0000550 · Cited by 13
“Brain autopsy studies reveal substantial AD pathology in a nontrivial number of aging individuals who did not seem to exhibit cognitive decline before death (DeTure & Dickson, 2019; Montine et al., 2012; Rodrigue, Kennedy, & Park, 2009).”
BackgroundGlobular glial tauopathy Type I presenting with behavioral variant frontotemporal dementia
Hirano, M., Iritani, S., Fujishiro, H., et al. (2020) · Neuropathology · doi:10.1111/neup.12668 · Cited by 12
Lachén-Montes, M., Mendizuri, N., Ausín, K., Pérez-Mediavilla, A., Azkargorta, M., Iloro, I., Elortza, F., Kondo, H., Ohigashi, I., Ferrer, I., et al. (2020) · Journal of Proteome Research · doi:10.1021/acs.jproteome.0c00452 · Cited by 12
Cousins, K. A. Q., Bove, J., Giannini, L., Kinney, N. G., Balgenorth, Y. R., Rascovsky, K., Lee, E. B., Trojanowski, J. Q., Grossman, M., & Irwin, D. J. (2021) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12188 · Cited by 10
Self-citationMelikyan, Z. A., Corrada, M. M., Leiby, A. C., Sajjadi, S. A., Bukhari, S. A., Montine, T. J., & Kawas, C. H. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2022.03.009 · Cited by 12
Self-citationvan Amerongen, S., Caton, D. K., Ossenkoppele, R., Barkhof, F., Pouwels, P. J. W., Teunissen, C. E., Rozemüller, A. J. M., Hoozemans, J. J. M., Pijnenburg, Y. A. L., Scheltens, P., et al. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-01059-8 · Cited by 13
Cognitive function in very old men does not correlate to biomarkers of Alzheimer’s disease
Veličkaitė, V., Giedraitis, V., Ström, K., Alafuzoff, I. I., Zetterberg, H., Lannfelt, L., Kilander, L., Larsson, E., & Ingelsson, M. (2017) · BMC Geriatrics · doi:10.1186/s12877-017-0601-6 · Cited by 12
“Two of the subjects with clinical diagnosis of AD fulfilled the NIA-AA criteria for high level of AD related pathology [34, 35].”
Shepherd, C. E., Affleck, A. J., Bahar, A. Y., Carew‐Jones, F., Gregory, G., Small, D. H., & Halliday, G. M. (2020) · Brain and Behavior · doi:10.1002/brb3.1672 · Cited by 11
Comparison of plasma ALZpath p-Tau217 with Lilly p-Tau217 and p-Tau181 in a neuropathological cohort
Bali, D., Salvadó, G., Beach, T. G., Serrano, G. E., Atri, A., Reiman, E. M., Jeromin, A., Hansson, O., & Janelidze, S. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-02064-2 · Cited by 14
“Participants were categorized into two groups based on the ADNC scale [34]; none/low ADNC ( n = 30, clinical diagnosis: 8 controls, 3 MCI, 19 non-AD neurodegenerative diseases) and intermediate/high ADNC ( n = 42, clinical diagnosis: 7 controls, 6 MCI, 14 AD, 15 non-AD neurodegenerative diseases).”
Self-citationErskine, D., & Taylor, J. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00856-7 · Cited by 16
“…at an intermediate stage based on consensus criteria for the neuropathological reporting of Alzheimer’s disease; however, up to 30% of DLB cases have a high level of Alzheimer-type neuropathological change, a level sufficient for a neuropathological diagnosis of Alzheimer’s disease [74, 76, 77].”
Lu, A., Chen, W.-T., Dalby, M., García, D. S., Vanheusden, M., de Vries, L. E., van Lieshout, V., Martirosyan, A., Craessaerts, K., Moonen, S., et al. (2026) · Nature Medicine · doi:10.1038/s41591-026-04393-8 · Cited by 22
Self-citationJosephs, K. A., Tosakulwong, N., Gatto, R. G., Weigand, S. D., Ali, F., Botha, H., Graff‐Radford, J., Machulda, M. M., Savica, R., Schwarz, C. G., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26479 · Cited by 13
“For the purpose of this study and guided by the National Institute of Aging–Alzheimer’s Association recommendations, we subclassified the 91 ADNC participants into high and low/intermediate (referred to from here onward as low) ADNC groups based on the following Braak NFT stages(33): low ADNC (n = 33, Braak NFT stage…”
MethodResultSelf-citationKim, B. J., Grossman, M., Alemán, T. S., Song, D., Cousins, K. A. Q., McMillan, C. T., Saludades, A., Yu, Y., Lee, E. B., Wolk, D. A., et al. (2023) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.01.015 · Cited by 13
Cortical iron accumulation in MAPT ‐ and C9orf 72‐associated frontotemporal lobar degeneration
Giannini, L. A. A., Bulk, M., Kenkhuis, B., Rajicic, A., Melhem, S., Hegeman-Kleinn, I. M., Bossoni, L., Suidgeest, E., Dopper, E. G. P., Swieten, J. C. V., et al. (2023) · Brain Pathology · doi:10.1111/bpa.13158 · Cited by 11
“Neuropathological diagnosis was established using established criteria [25–27], the occurrence of age-related copathology was noted and is reported in this article as ABC score [26].”
MethodBiswas, R., Kawas, C. H., Montine, T. J., Bukhari, S. A., Jiang, L., & Corrada, M. M. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-221062 · Cited by 11
Self-citationAn Autopsy Series of Seven Cases of VPS13A Disease (Chorea‐Acanthocytosis)
Ditzel, R. M., Walker, R. H., Nirenberg, M. J., Tetlow, A. M., Farrell, K. W., Lind‐Watson, K. J., Thorn, E. L., Dangoor, D. K., Gordon, R., Sanctis, C. D., et al. (2023) · Movement Disorders · doi:10.1002/mds.29589 · Cited by 11
Association between military service and Alzheimer's disease neuropathology at autopsy
Powell, W. R., Vilen, L. H., Zuelsdorff, M. L., Goutman, S. A., Salamat, S. M., Rissman, R. A., Bendlin, B. B., & Kind, A. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.13520 · Cited by 9
Lee, H., Fu, J. F., Gaudet, K., Bryant, A. G., Price, J. C., Bennett, R. E., Johnson, K. A., Hyman, B. T., Hedden, T., Salat, D. H., et al. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231216144 · Cited by 11
Self-citationNeuropathologic Burden and Dementia in Nonagenarians and Centenarians
Cholerton, B., Latimer, C. S., Crane, P. K., Corrada, M. M., Gibbons, L. E., Larson, E. B., Kawas, C. H., Keene, C. D., & Montine, T. J. (2024) · Neurology · doi:10.1212/wnl.0000000000208060 · Cited by 13
Self-citationMcInvale, J. J., Canoll, P., & Hargus, G. (2024) · Brain Pathology · doi:10.1111/bpa.13231 · Cited by 11
Yamakawa, M., & Rexach, J. E. (2024) · Biomedicines · doi:10.3390/biomedicines12020308 · Cited by 14
“As per Gabitto et al., Lewy body disease scores were based on the National Institute on Aging guidelines [27–29].”
MethodAge-Related Pathology in Corticobasal Degeneration
Mimuro, M., & Iwasaki, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052740 · Cited by 11
Sakurai, K., Tokumaru, A. M., Yoshida, M., Saito, Y., Wakabayashi, K., Komori, T., Hasegawa, M., Ikeuchi, T., Hayashi, Y., Shimohata, T., et al. (2024) · Neuroradiology · doi:10.1007/s00234-024-03432-w · Cited by 11
Bentivenga, G. M., Baiardi, S., Mastrangelo, A., Ruggeri, E., Mammana, A., Ticca, A., Rossi, M., Capellari, S., & Parchi, P. (2024) · Alzheimer s Research & Therapy · doi:10.1186/s13195-024-01565-x · Cited by 13
“…(p-tau) (AT8, dilution 1:100, Innogenetics), Aβ (4G8, dilution 1:5000, Signet Labs), prion protein (3F4, dilution 1:400, Signet Labs), and TDP-43 (409/410, dilution 1:5000, Cosmo Bio) was applied to all cases using several brain regions, following established consensus criteria [14–16 , 24].”
MethodA Map of Transcriptomic Signatures of Different Brain Areas in Alzheimer’s Disease
Ferrari, R. R., Fantini, V., Garofalo, M., Di Gerlando, R., Dragoni, F., Rizzo, B., Spina, E., Rossi, M., Calatozzolo, C., Profka, X., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011117 · Cited by 14
Dziewa, M., Złotek, M., Herbet, M., & Piątkowska‐Chmiel, I. (2024) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-024-01514-0 · Cited by 11
MIND Diet and Hippocampal Sclerosis Among Community-Based Older Adults
Agarwal, P., Agrawal, S., Wagner, M., Cherian, L. J., Aggarwal, N. T., James, B. D., Holland, T. M., Bennett, D. A., Barnes, L. L., Leurgans, S. E., et al. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.26089 · Cited by 17
Self-citationBuck, S. A., Malankhanova, T. B., Strader, S., Eileen, B., Yim, S., Pratt, H. W., Ervin, J. F., Lee, E. B., Wang, S. J., Cohen, T. J., et al. (2025) · Acta Neuropathologica · doi:10.1007/s00401-025-02951-x · Cited by 13
“…tangle stage, CERAD neuritic plaque score, LBD (McKeith DLB), limbic-predominant age-related TDP-43 encephalopathy neurological change (LATE-NC), small vessel disease, and age-related tau astrogliopathy (ARTAG) were performed according to published guidelines [12, 65, 75, 79, 83, 86, 104, 113].”
Chen, D., Latimer, C. S., Spencer, M. W., Karna, P., Gonzalez‐Cuyar, L. F., Davis, M. Y., Keene, C. D., Bird, T. D., & Raskind, W. H. (2019) · Movement Disorders Clinical Practice · doi:10.1002/mdc3.12873 · Cited by 12
Neocortical Neurofibrillary Degeneration in Primary Age-Related Tauopathy
Walker, J. M., White, C. L., Farrell, K. W., Crary, J. F., & Richardson, T. E. (2021) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlab113 · Cited by 12
Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains
Poloni, T. E., Medici, V., Carlos, A. F., Davin, A., Ceretti, A., Mangieri, M., Cassini, P., Vaccaro, R., Zaccaria, D., Abbondanza, S., et al. (2020) · Journal of Visualized Experiments · doi:10.3791/60296-v · Cited by 11
Handa, T., Sasaki, H., Takao, M., Tano, M., & Uchida, Y. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00351-x · Cited by 13
“National Institute on Aging-Alzheimer’s Association (NIA-AA) guidelines (2012) were applied to determine the level of AD pathological change [4] on the basis of a previously described neuropathological analysis [5].”
MethodMichno, W., Koutarapu, S., Camacho, R., Toomey, C. E., Stringer, K. M., Minta, K., Ge, J., Jha, D., Fernández-Rodrı́guez, J., Brinkmalm, G., et al. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15694 · Cited by 9
“The CAA + exhibited moderate to high A β pathology but was not diagnosed as AD due to the restricted tau and A β plaque pathology (Braak & Braak, 1991 ; Montine et al., 2012; Thal et al., 2002 ).”
Characterization of spastic paraplegia in a family with a novelPSEN1mutation
Ringman, J. M., Dorrani, N., Fernández, S. G., Signer, R. H., Martínez-Agosto, J. A., Lee, H., Douine, E. D., Qiao, Y., Shi, Y., D’Orazio, L. M., et al. (2023) · Brain Communications · doi:10.1093/braincomms/fcad030 · Cited by 11
“Neuropathologic substrates of dementia were assessed using standard diagnostic criteria.(19) The presence of cerebrovascular disease was also evaluated, including cerebral amyloid angiopathy (CAA) graded according to the Vonsattel criteria.”
BackgroundMethodSelf-citationMahady, L. J., Perez, S. E., Malek‐Ahmadi, M. H., & Mufson, E. J. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25466 · Cited by 11
“The UKADC has not re-evaluated these cases using the revised NIA–Alzheimer’s Association neuropathological criteria (Montine et al., 2012) or the inclusion of biomarkers with these guidelines (Jack et al., 2018).”
MethodUeberham, U., Rohn, S., Ueberham, E., Wodischeck, S., Hilbrich, I., Holzer, M., Brückner, M. K., Gruschka, H., & Arendt, T. (2014) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12163 · Cited by 11
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old
Ghoshal, N., Perry, A., McKeel, D. W., et al. (2014) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0000000000000049 · Cited by 11
Self-citationEndothelin‐converting enzymes degrade α‐synuclein and are reduced in dementia with Lewy bodies
Miners, J. S., & Love, S. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.13974 · Cited by 10
Keene, C. D., Wilson, A. M., Kilgore, M. D., Bruner, L. T., Postupna, N. O., & Darvas, M. (2018) · Laboratory Investigation · doi:10.1038/s41374-018-0165-x · Cited by 11
Globular glial tauopathy Type II: Clinicopathological study of two autopsy cases
Tanaka, H., Kawakatsu, S., Toyoshima, Y., et al. (2019) · Neuropathology · doi:10.1111/neup.12532 · Cited by 11
“†Neuronal tau pathology (grade 2) of the transentorhinal cortex in case 1 mainly reflects Alzheimer pathology (Alzheimer’s disease neuropathologic change: low (A1, B1, C0)).(13)”
BackgroundTDP‐43 in the olfactory bulb in Alzheimer's disease
Josephs, K. A., & Dickson, D. W. (2016) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12309 · Cited by 11
Self-citationIwasaki, Y., Mori, K., Ito, M., et al. (2017) · Neuropathology · doi:10.1111/neup.12399 · Cited by 11
Liu‐Seifert, H., Siemers, E., Sundell, K., Mynderse, M., Cummings, J. L., Mohs, R. C., & Aisen, P. S. S. (2018) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2018.22 · Cited by 11
“Pathologic hallmarks of AD identified at autopsy include the presence of neuritic amyloid beta peptide (Aβ) plaques, neurofibrillary tangles, and neuronal loss in brain regions important for cognition, such as the hippocampus and temporal cortex (1).”
BackgroundBraun, M., Simon, M. J., Jang, J., Sanderson, K., Swierz, J., Sevao, M., Pincus, A. B., Schaser, A. J., Elliott, J. E., Lim, M. M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.14.607971 · Cited by 12
Antioxidants Against Neurological Disorders
Narang, J. K., Dogra, A., Kaur, T., Narang, R. S., & Singh, A. P. (2024) · Antioxidants · doi:10.1002/9781394270576.ch9 · Cited by 12
Tomé, S. O., Gawor, K., Ospitalieri, S., Ronisz, A., Otto, M., Arnim, C. A. F. V., Ghebremedhin, E., Laureyssen, C., Sleegers, K., Vandenberghe, R. R., et al. (2025) · Acta Neuropathologica · doi:10.1007/s00401-025-02929-9 · Cited by 13
“C on s e n s u s c r it e r i a a nd / o r gu i d e li n e s u s e d f o r eac h p a r a m e t e r : C D R S c o r e [ 37 ] , B r aa k N F T s t a g e s [ 40 , 86 ] , A β ph a s e s [ 43 ] , C E R AD s c o r e [ 42 ] d e g r ee o f ADN C a s p e r N I A - AA [ 35 ] , L A TE -”
Self-citationVrillon, A., Spina, S., Mejía‐Perez, J. A., LaMore, T., Yballa, C., Soleimani‐Meigooni, D. N., Blazhenets, G., Boxer, A. L., Rojas, J. C., Lago, A. L., et al. (2026) · Neurology · doi:10.1212/wnl.0000000000214576 · Cited by 14
Altered Gene Expression Within the Renin–Angiotensin System in Normal Aging and Dementia
Tayler, H. M., MacLachlan, R. A., Güzel, Ö., Fisher, R. A., Skrobot, O. A., Abulfadl, M. A., Kehoe, P. G., & Miners, J. S. (2023) · The Journals of Gerontology Series A · doi:10.1093/gerona/glad241 · Cited by 11
Chen, X., Walton, K. L., Brodaty, H., & Chalton, K. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231222 · Cited by 10
“The hallmarks of neuropathologic changes are neuritic plaques associated with neuronal injury, extracellular deposition of amyloid-(cid:2) (A (cid:2) ) peptides, and neurofibrillary degeneration such as neurofibrillary tangles [9, 10].”
Comorbid neuropathology and atypical presentation of Alzheimer's disease
Piña‐Escudero, S. D., Joie, R. L., Spina, S., Hwang, J., Miller, Z., Huang, E. J., Grant, H. E., Mundada, N. S., Boxer, A. L., Gorno‐Tempini, M., et al. (2024) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1002/dad2.12602 · Cited by 10
New criteria to predict LATE-NC in the clinical setting: Probable/Possible LATE and LANS
Nelson, P. T. (2024) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlae113 · Cited by 10
Self-citationBrain aging and Alzheimer’s disease, a perspective from non-human primates
Ferrer, I. (2024) · Aging · doi:10.18632/aging.206143 · Cited by 10
Medial temporal atrophy predicts the limbic comorbidities in lewy body disease
Sakurai, K., Kaneda, D., Morimoto, S., Uchida, Y., Inui, S., Shang, C., Kimura, Y., Cai, C., Kato, T., Ito, K., et al. (2024) · Neuroradiology · doi:10.1007/s00234-024-03502-z · Cited by 10
Cerebral amyloid angiopathy impacts neurofibrillary tangle burden and cognition
Godrich, D., Pasteris, J., Martin, E. R., Rundek, T., Schellenberg, G. D., Foroud, T., Vance, J. M., Pericak‐Vance, M. A., Cuccaro, M. L., Scott, W. K., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae369 · Cited by 12
Self-citationCo‐pathologies modify hippocampal protein accumulation patterns in neurodegenerative diseases
Yoshida, K., Forrest, S. L., Ichimata, S., Tanaka, H., Kon, T., & Kovács, G. G. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.14355 · Cited by 9
“31 The severity of Lewy-related pathology was assessed following the Lewy disease consensus criteria ).”
Müller, D., Röhr, D., Boon, B. D. C., Wulf, M., Arto, T., Hoozemans, J. J. M., Marcus, K., Rozemüller, A. J. M., Großerueschkamp, F., Axel Mosig, A., et al. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e42111 · Cited by 10
“AD cases (n = 16) were selected when clinical and neuropathological information fulfilled the criteria of the National Institute on Aging-Alzheimer ’ s Association (NIA-AA) for AD [65].”
Ono, D., Sekiya, H., Maier, A. R., Murray, M. E., Koga, S., & Dickson, D. W. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.14628 · Cited by 12
Self-citationCell-death pathways and tau-associated neuronal vulnerability in Alzheimer’s disease
Lin, G., Chancellor, S. E., Kwon, T., Woodbury, M. E., Doering, A., Abdourahman, A., Bennett, R. E., Liao, F., Pastika, T., Tamm, J. A., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115758 · Cited by 15
Self-citationAging-dependent YAP1 reduction contributes to AD pathology by upregulating the Nr4a1-AKT/GSK-3β axis
Lei, L., Cheng, Y., Yin, A., Han, J.-M., Wu, G., Yang, F., Wang, Q., Wang, J., Liu, R., Li, H., et al. (2025) · Translational Neurodegeneration · doi:10.1186/s40035-025-00487-4 · Cited by 13
“Senile plaques composed of extracellular β-amyloid (Aβ) deposits, and neurofibrillary tangles (NFTs) formed by intracellular accumulation/deposition of hyperphosphorylated tau proteins, are two neuropathological features of AD [13, 14].”
Holmes, B. B., Weigel, T. K., Chung, J. M., Kaufman, S. K., Apresa, B. I., Byrnes, J. R., Kumru, K. S., Vaquer‐Alicea, J., Gupta, A., Rose, I. V. L., et al. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00883-4 · Cited by 14
“Neuropathological diagnoses were made following consensus diagnostic criteria [90] using previously described histological and immunohistochemical methods [91, 92, 93].”
Amyloidosis of bridging veins is a pathologic feature of Alzheimer’s disease
Smyth, L. C. D., Verhaege, D., Standen-Bloom, E., Wu, Y., Gan, Y., Storck, S. E., Boskovic, P., Plog, B. A., Mamuladze, T., Mazzitelli, J. A., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20251860 · Cited by 11
Tosoni, G., Ayyildiz, D., Snoeck, S., Moreno‐Jiménez, E. P., Penning, A., Santiago-Mujika, E., Ormaechea, O. R., Lee, H., Poovathingal, S. K., Davie, K., et al. (2026) · Cell stem cell · doi:10.1016/j.stem.2026.04.002 · Cited by 13
Hippocampal Laminar Distribution of Tau Relates to Alzheimer's Disease and Age of Onset
Seifan, A., Marder, K. S., Mez, J. B., Noble, J. M., Cortes, E. P., Vonsattel, J. P., & Honig, L. S. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-140279 · Cited by 10
“Alzheimer's disease (AD) is marked neuropathologically by cerebral deposits of plaques, containing amyloid-β, and tangles and threads containing abnormally phosphorylated tau protein (phospho-tau) [1].”
Mao, P. (2012) · Advances in Biological Chemistry · doi:10.4236/abc.2012.22022 · Cited by 10
“NIA-AA recently recommends that LBD (Lewy body diseases, including Parkinson disease and dementia with Lewy bodies) be classified as no LBs, brainstem predominant, limbic (transitional), neocortical (diffuse), or amygdala predominant [13,71].”
BackgroundProteolytic Cleavage of Apolipoprotein E in the Down Syndrome Brain
Day, R. J., McCarty, K. L., Ockerse, K. E., Head, E., & Rohn, T. T. (2016) · Aging and Disease · doi:10.14336/ad.2015.1020 · Cited by 10
“AD was established in DS cases based upon published consensus neuropathological criteria [25].”
MethodDiagnosis of Alzheimer’s—Standard-of-Care
Lewis, T. J., & Trempe, C. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812112-2.00003-3 · Cited by 10
Co-occurrence of chronic traumatic encephalopathy and prion disease
Nemani, S. K., Notari, S., Calì, I., Alvarez, V. E., Kofskey, D., Cohen, M. L., Stern, R. A., Appleby, B. S., Abrams, J. Y., Schonberger, L. B., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0643-9 · Cited by 12
Tan, R. H., Yang, Y., McCann, H., Shepherd, C. E., & Halliday, G. M. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180900 · Cited by 8
Blazhenets, G., Frings, L., Sörensen, A., & Meyer, P. T. (2020) · Journal of Nuclear Medicine · doi:10.2967/jnumed.120.252783 · Cited by 10
“Therefore, we investigated the relationship between (18)F-FDG- and Ab-ADCRP and neuropathology findings as expressed by Braak stage of NFTs (10) and Thal amyloid phase for neuritic plaques (11), respectively, and the value of individual and combined measures to identify the AD neuropathologic change (ADNC) stages (12).”
BackgroundMethodAre the 50’s, the transition decade, in choroid plexus aging?
Tahira, A. C., Marques, F., Lisbôa, B. C. G., Feltrin, A. S., Barbosa, A. D. L., Oliveira, K. C., Pereira, C. A. D. B., Leite, R. E. P., Grinberg, L. T., Suemoto, C. K., et al. (2021) · GeroScience · doi:10.1007/s11357-021-00329-x · Cited by 14
Cash, M. K., Rockwood, K. J., Fisk, J. D., & Darvesh, S. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.02.025 · Cited by 11
Hasan, M. F., & Trushina, E. V. (2022) · Brain Sciences · doi:10.3390/brainsci12050552 · Cited by 10
“AD is marked by initial episodic memory loss and gradual severe cognitive decline [32].”
BackgroundKawakatsu, S., Kobayashi, R., Morioka, D., Hayashi, H., Utsunomiya, A., Kabasawa, T., Ohe, R., Futakuchi, M., & Otani, K. (2022) · Neuropathology · doi:10.1111/neup.12859 · Cited by 10
“AD neuropathological changes were evaluated using the “ABC” score.(24) Neuropathological diagnosis of dementia with Lewy bodies (DLB) was based on the criteria by McKeith et al.”
MethodAumont, É., Tremblay, C., Levert, S., Bennett, D. A., Calon, F., & Leclerc, N. M. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1038343 · Cited by 10
“This is opposed to individuals with not or low levels of AD neuropathological changes, for whom AD neuropathology is insufficient to account for any cognitive symptom (N = 20; 10 NCI, 8 MCI and 2 with dementia; Montine et al., 2012).”
BackgroundMethodInfluentialSuchy‐Dicey, A. M., Su, Y., Buchwald, D., Manson, S. M., & Reiman, E. M. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12889 · Cited by 10
Pillai, J. A., Bena, J., Maly, E. F., & Leverenz, J. B. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.12922 · Cited by 9
Walker, C. K., Greathouse, K. M., Tuscher, J. J., Dammer, E. B., Weber, A. J., Liu, E., Curtis, K. A., Boros, B. D., Freeman, C. D., Seo, J. V., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2102-22.2023 · Cited by 12
“The Amyloid Braak CERAD (ABC) score (none, low, intermediate, high) was used as a global measure of AD pathology (Montine et al., 2012).”
MethodTargeting the post-synaptic proteome has therapeutic potential for psychosis in Alzheimer Disease
Krivinko, J. M., DeChellis-Marks, M. R., Zeng, L., Fan, P., López, O. L., Ding, Y., Wang, L., Kofler, J., MacDonald, M. L., & Sweet, R. A. (2023) · Communications Biology · doi:10.1038/s42003-023-04961-5 · Cited by 10
“MVLs were enumerated in standardized sections 38 of middle frontal gyrus (DLPFC), superior and middle temporal gyrus, inferior parietal lobule, occipital cortex (BA 17/18), basal ganglia at level of anterior commissure, and thalamus at the level of the subthalamic nucleus to create MVL counts.”
Darvesh, S., Banfield, S. C., Dufour, M., Forrestall, K. L., Maillet, H., Reid, G. A., Sands, D. C., & Pottie, I. R. (2023) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2023.2225797 · Cited by 10
Chong, J. R., Chai, Y. L., Xing, H., Herr, D. R., Wenk, M. R., Francis, P. T., Ballard, C. G., Aarsland, D., Silver, D. L., Chen, C., et al. (2023) · Brain Pathology · doi:10.1111/bpa.13190 · Cited by 10
“…into hemi-spheres, with one formalin-fixed for neuropathological assessments, which included the National Institute on Aging-Alzheimer ’ s Association guidelines with phases of A β deposition, Braak stages, and CERAD scores [37 – 39], as well as the Newcastle/McKeith criteria for LB disease [34].”
Method
Metadata
- Authors
- Montine, T. J., Phelps, C. H., Beach, T. G., Bigio, E. H., Cairns, N. J., Dickson, D. W., Duyckaerts, C., Frosch, M. P., Masliah, E., Mirra, S. S., Nelson, P. T., Schneider, J. A., Thal, D. R., Trojanowski, J. Q., Vinters, H. V., & Hyman, B. T.
- Affiliations
- University of Washington (US)
- National Institutes of Health (US)
- Banner Sun Health Research Institute (US)
- Northwestern University (US)
- Washington University in St. Louis (US)
- Mayo Clinic (US)
- Pitié-Salpêtrière Hospital (FR)
- Harvard University (US)
- University of California San Diego (US)
- SUNY Downstate Health Sciences University (US)
- University of Kentucky (US)
- Rush University Medical Center (US)
- Universität Ulm (DE)
- University of Pennsylvania (US)
- University of California, Los Angeles (US)
- Corresponding author
- Montine, Thomas J.
- ORCID
- Venue
- Acta Neuropathologica
- Published
- 2011-11-20
- Volume
- 123
- Issue
- 1
- Pages
- 1-11
- ISSN
- 0001-6322 (ISSN-L)
- 1432-0533
- PMC
- PMC3268003
- OpenAlex
- W2128228199
- Cited by
- 2,894
- References
- 66
- Citations by year
- 2026: 254 · 2025: 290 · 2024: 329 · 2023: 251 · 2022: 284 · 2021: 257 · 2020: 244 · 2019: 183 · 2018: 164 · 2017: 148 · 2016: 144 · 2015: 136 · 2014: 92 · 2013: 69 · 2012: 46
- FWCI
- 39.19
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Acta Neuropathologica (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5u01ag024904-10)
- National Institute on Aging (U01-AG-024904, R01AG017917, AG18840, AG-15819, R01AG015866, P30AG028383, R01AG042210, R01AG018440, U01AG016976, P50AG005131, P50AG016570, P01AG003949, P30AG010124, R01AG015819, P30AG010161, AG24904, P50AG005681, P30AG019610, P01AG003991, P50AG005136, P50AG005134, P30AG013854, U19AG010483, RF1AG015819, P01AG012435, U19AG024904, P30AG062421)
- National Institute of Neurological Disorders and Stroke (P50NS062684)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, amyloid-beta deposition, neurofibrillary tangles, neuritic plaques, ABC score, Lewy body disease, vascular brain injury, hippocampal sclerosis, TDP-43 inclusions, staining techniques, clinicopathological correlation, preclinical Alzheimer's disease
- MeSH terms
- Alzheimer Disease, Brain, Cerebrovascular Disorders, DNA-Binding Proteins, Hippocampus, Humans, Sclerosis, United States, Cerebrovascular Trauma, Lewy Body Disease, National Institute on Aging (U.S.)
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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.
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