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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2003 1
2005 1
2006 1
2007 1
2008 1
2011 1
2014 2
2015 3
2017 3
2018 2
2019 2
2020 3
2021 4
2022 3
2023 2
2024 1

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29 results

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Page 1
Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation.
Uttley L, Carroll C, Wong R, Hilton DA, Stevenson M. Uttley L, et al. Lancet Infect Dis. 2020 Jan;20(1):e2-e10. doi: 10.1016/S1473-3099(19)30615-2. Lancet Infect Dis. 2020. PMID: 31876504 Free article.
Creutzfeldt-Jakob disease (CJD) is a fatal disease presenting with rapidly progressive dementia, and most patients die within a year of clinical onset. ...
Creutzfeldt-Jakob disease (CJD) is a fatal disease presenting with rapidly progressive dementia, and most patients die …
Tics in patients with encephalitis.
Badenoch J, Searle T, Watson I, Cavanna AE. Badenoch J, et al. Neurol Sci. 2021 Apr;42(4):1311-1323. doi: 10.1007/s10072-021-05065-w. Epub 2021 Jan 23. Neurol Sci. 2021. PMID: 33486621 Free PMC article. Review.
RESULTS: In addition to the established association between tics and encephalitis lethargica, our literature search identified reports of tics in patients with immune-mediated pathologies (including autoimmune encephalitides affecting the N-methyl-D-aspartate receptor, voltage-ga …
RESULTS: In addition to the established association between tics and encephalitis lethargica, our literature search identified reports of ti …
Systematic review of pharmacological management in Creutzfeldt-Jakob disease: no options so far?
Miranda LHL, Oliveira AFPH, Carvalho DM, Souza GMF, Magalhães JGM, Júnior JAC, Lima PTMBQ, Júnior RMA, Filho SPL, Melo HMA. Miranda LHL, et al. Arq Neuropsiquiatr. 2022 Aug;80(8):837-844. doi: 10.1055/s-0042-1755341. Epub 2022 Oct 17. Arq Neuropsiquiatr. 2022. PMID: 36252593 Free PMC article. Review.
BACKGROUND: The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive dementia syndrome. ...The Medical Subject Heading (MeSH) terms used were: prion diseases, Creutzfeldt-Jakob disease, ph …
BACKGROUND: The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive …
Risk of acquiring Creutzfeldt-Jakob disease from blood transfusions: systematic review of case-control studies.
Wilson K, Code C, Ricketts MN. Wilson K, et al. BMJ. 2000 Jul 1;321(7252):17-9. doi: 10.1136/bmj.321.7252.17. BMJ. 2000. PMID: 10875826 Free PMC article. Review.
Three of the five studies used medical or neurological patients as controls, the other two used population controls. Odds ratios for developing Creutzfeldt-Jakob disease from blood transfusion ranged from 0.54 to 0.89. ...CONCLUSIONS: Case-control studies do …
Three of the five studies used medical or neurological patients as controls, the other two used population controls. Odds ratios for develop …
Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt-Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene.
Matsubayashi T, Sanjo N. Matsubayashi T, et al. Int J Mol Sci. 2022 Dec 2;23(23):15172. doi: 10.3390/ijms232315172. Int J Mol Sci. 2022. PMID: 36499498 Free PMC article. Review.
Genetic Creutzfeldt-Jakob disease (gCJD) is a subtype of genetic prion diseases (gPrDs) caused by the accumulation of mutated pathological prion proteins (PrP(Sc)). gCJD has a phenotypic similarity with sporadic CJD (sCJD). ...
Genetic Creutzfeldt-Jakob disease (gCJD) is a subtype of genetic prion diseases (gPrDs) caused by the accumulation of m …
Risk of transmission of sporadic Creutzfeldt-Jakob disease by surgical procedures: systematic reviews and quality of evidence.
López FJG, Ruiz-Tovar M, Almazán-Isla J, Alcalde-Cabero E, Calero M, de Pedro-Cuesta J. López FJG, et al. Euro Surveill. 2017 Oct;22(43):16-00806. doi: 10.2807/1560-7917.ES.2017.22.43.16-00806. Euro Surveill. 2017. PMID: 29090678 Free PMC article. Review.
BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is potentially transmissible to humans. ...
BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is potentially transmissible to humans. ...
Understanding Creutzfeldt-Jakob disease in Iran: a systematic review of case reports.
Mohebbi A, Motamedaria P, Naderi M, Hassanpour M, Salavatiha Z, Makouei M, Ataei-Pirkooh A. Mohebbi A, et al. J Int Med Res. 2024 May;52(5):3000605241247706. doi: 10.1177/03000605241247706. J Int Med Res. 2024. PMID: 38717041 Free PMC article.
OBJECTIVE: To systematically review the reported cases of Creutzfeldt-Jakob disease (CJD) in Iran. METHODS: A comprehensive literature review of CJD cases in Iran was undertaken using the PubMed, Scopus and Google Scholar databases. ...
OBJECTIVE: To systematically review the reported cases of Creutzfeldt-Jakob disease (CJD) in Iran. METHODS: A comprehen …
Diagnostic Utility of Cerebrospinal Fluid alpha-Synuclein in Creutzfeldt-Jakob Disease: A Systematic Review and Meta-Analysis.
Kong Y, Chen Z, Wang X, Wang W, Zhang J. Kong Y, et al. J Alzheimers Dis. 2022;89(2):493-503. doi: 10.3233/JAD-220425. J Alzheimers Dis. 2022. PMID: 35912746
BACKGROUND: Creutzfeldt-Jakob disease (CJD) can be difficult to distinguish clinically from some non-prion neurological diseases. ...
BACKGROUND: Creutzfeldt-Jakob disease (CJD) can be difficult to distinguish clinically from some non-prion neurological …
Current evidence on the transmissibility of chronic wasting disease prions to humans-A systematic review.
Waddell L, Greig J, Mascarenhas M, Otten A, Corrin T, Hierlihy K. Waddell L, et al. Transbound Emerg Dis. 2018 Feb;65(1):37-49. doi: 10.1111/tbed.12612. Epub 2017 Jan 30. Transbound Emerg Dis. 2018. PMID: 28139079 Review.
A number of prion diseases affect humans, including Creutzfeldt-Jakob disease; most of these are due to genetic mutations in the affected individual and occur sporadically, but some result from transmission of prion proteins from external sources. ...
A number of prion diseases affect humans, including Creutzfeldt-Jakob disease; most of these are due to genetic mutatio …
29 results