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A new variant of Creutzfeldt-Jakob disease in the UK
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Research works printed but not linked: 16
- Cousens, 1990, Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84, J Neurol Neurosurg Psych, 53, 459, 10.1136/jnnp.53.6.459 · DOI
- Delasnerie-Laupretre, 1995, Incidence of Creutzfeldt-Jakob disease in Europe, Lancet, 346, 898, 10.1016/S0140-6736(95)92735-2 · doi:10.1016/s0140-6736(95)92735-2
- Goodbrand, 1995, Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob disease, Neurosci Lett, 183, 127, 10.1016/0304-3940(94)11131-2 · DOI · Paper page
- Britton, 1995, Sporadic Creutzfeldt-Jakob disease in a 16-year old in the UK, Lancet, 346, 1155, 10.1016/S0140-6736(95)91827-2 · DOI
- Bateman, 1995, Sporadic Creutzfeldt-Jakob disease in a 18-year old in the UK, Lancet, 346, 1155, 10.1016/S0140-6736(95)91828-0 · DOI
- Budka, 1995, Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases), Brain Pathology, 5, 459, 10.1111/j.1750-3639.1995.tb00625.x · DOI · Paper page
- Bell, 1993, Neuropathology of spongiform encephalopathies in humans, Brit Med Bull, 49, 738, 10.1093/oxfordjournals.bmb.a072645 · DOI
- Monreal, 1981, Creutzfeldt-Jakob disease in an adolescent, J Neuro Sciences, 52, 341, 10.1016/0022-510X(81)90015-0 · DOI
- Brown, 1985, Epidemiologic implications of Creutzfeldt-Jakob disease in a 19-year-old girl, Euro J Epid, 1, 42, 10.1007/BF00162311 · doi:10.1007/bf00162311
- Packer, 1980, Creutzfeldt-Jakob disease in a 20-year-old woman, Neurology, 30, 492, 10.1212/WNL.30.5.492 · doi:10.1212/wnl.30.5.492
- Berman, 1988, Progressive neurological deterioration in a 14-year-old girl, Pediatr Neurosci, 14, 42, 10.1159/000120361 · doi:10.1159/000120361
- Weller, 1986, Pathology of Creutzfeldt-Jakob disease associated with pituitary-derived human growth hormone administration, Neuropathol Appl Neurobiol, 12, 117, 10.1111/j.1365-2990.1986.tb00045.x · DOI
- Brown, 1987, The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature, Neurology, 37, 895, 10.1212/WNL.37.6.895 · DOI · Paper page
- Kulczycki, 1991, Creutzfeldt-Jakob disease in young people, European J Epid, 7, 501, 10.1007/BF00143129 · doi:10.1007/bf00143129
- Bruce, 1991, The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis, J Gen Virol, 72, 595, 10.1099/0022-1317-72-3-595 · DOI · Paper page
- Howard, 1996, Creutzfeldt-Jakob disease in a young woman, Lancet, 347, 945, 10.1016/S0140-6736(96)91419-1 · DOI
Cited by
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Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
Collinge, J., Sidle, K. C. L., Meads, J., Ironside, J., & Hill, A. F. (1996) · Nature · doi:10.1038/383685a0 · Cited by 1,735
Self-citationPrion Diseases of Humans and Animals: Their Causes and Molecular Basis
Collinge, J. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.519 · Cited by 1,344
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Metadata
- Authors
- Will, R. G., Ironside, J. W., Zeidler, M., Estibeiro, K., Cousens, S. N., Smith, P. G., Alperovitch, A., Poser, S., Pocchiari, M., & Hofman, A.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 1996-04
- Volume
- 347
- Issue
- 9006
- Pages
- 921-925
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2082573664
- Cited by
- 2,707
- References
- 0
- FWCI
- 52.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
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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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- CoChat. (2026). Citation check: A new variant of Creutzfeldt-Jakob disease in the UK. https://app.cochat.ai/papers/10.1016/s0140-6736(96)91412-9
- The paper
- Will, R. G., Ironside, J. W., Zeidler, M., Estibeiro, K., Cousens, S. N., Smith, P. G., Alperovitch, A., Poser, S., Pocchiari, M., & Hofman, A. (1996). A new variant of Creutzfeldt-Jakob disease in the UK. The Lancet. https://doi.org/10.1016/s0140-6736(96)91412-9
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
