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Year Number of Results
2000 1
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2008 1
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2014 2
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2017 2
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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. ...In this Review, we sought evidence to understand the current iatrogenic risk of CJD to public hea …
Creutzfeldt-Jakob disease (CJD) is a fatal disease presenting with rapidly progressive dementia, and most patien …
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 …
BACKGROUND: The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive …
How common are seizures in the heidenhain variant of creutzfeldt-jakob disease? A case report and systematic review.
Muthusamy S, Garg P, Chandra RV, Seneviratne U. Muthusamy S, et al. J Clin Neurosci. 2021 Apr;86:301-309. doi: 10.1016/j.jocn.2020.10.002. Epub 2021 Jan 9. J Clin Neurosci. 2021. PMID: 33436304
The Heidenhain variant of Creutzfeld-Jakob disease (HvCJD) is a relentlessly progressive and fatal neurodegenerative disorder characterised by prominent visual features early in its clinical course. ...A systematic search of the databases Medline, PubMed, and …
The Heidenhain variant of Creutzfeld-Jakob disease (HvCJD) is a relentlessly progressive and fatal neurodegenerative di …
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 …
Creutzfeldt-Jakob Disease Presenting as Stroke: A Case Report and Systematic Literature Review.
Sharma DK, Boggild M, van Heuven AW, White RP. Sharma DK, et al. Neurologist. 2017 Mar;22(2):48-53. doi: 10.1097/NRL.0000000000000107. Neurologist. 2017. PMID: 28248914 Review.
BACKGROUND: Creutzfeldt-Jacob disease (CJD) is a human prion disease generally characterized by subacute changes in behavior and intellectual function, often followed by ataxia, vision changes, and myoclonus. ...RESULTS: A 68-year-old woman presented with an …
BACKGROUND: Creutzfeldt-Jacob disease (CJD) is a human prion disease generally characterized by subacute changes in beh …
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. ...A single case-control study with a low risk of bias found a strong association between surgery conducted more than 20 years before disease onset and sCJD. …
BACKGROUND: Sporadic Creutzfeldt-Jakob disease (sCJD) is potentially transmissible to humans. ...A single case-control …
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. ...METHODS: The Ovid MEDLINE, Cochrane, and Embase databases were searched for articles published on or before February 25, 2022, …
BACKGROUND: Creutzfeldt-Jakob disease (CJD) can be difficult to distinguish clinically from some non-prion neurological …
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 …
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 …
Variant Creutzfeldt-Jakob disease: a cause for concern. Review of the evidence for risk of transmission through abdominal lymphoreticular tissue surgery.
Olsen SB, Sheikh A, Peck D, Darzi A. Olsen SB, et al. Surg Endosc. 2005 Jun;19(6):747-50. doi: 10.1007/s00464-004-9205-2. Epub 2005 May 4. Surg Endosc. 2005. PMID: 15868249 Review.
BACKGROUND: Concern has long existed regarding the possible iatrogenic spread of variant Creutzfeldt-Jakob disease (v-CJD) through surgery. This had been fueled by recent reports of bovine spongiform encephalopathy in U.S. cattle and the first probable …
BACKGROUND: Concern has long existed regarding the possible iatrogenic spread of variant Creutzfeldt-Jakob disease …
25 results