Young-onset sporadic Creutzfeldt–Jakob disease with atypical phenotypic features: a case report-Reference-Cited by-同舟云学术

Young-onset sporadic Creutzfeldt–Jakob disease with atypical phenotypic features: a case report

Published:2019-05-29 Issue:1 Volume:13 Page:
ISSN:1752-1947
Container-title:Journal of Medical Case Reports
language:en
Short-container-title:J Med Case Reports

Author:

Lahiri Durjoy,Pattnaik Srimant,Bhat Ashwani,Dubey Souvik,Biswas Atanu,Roy Biman Kanti

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13256-019-2089-5.pdf

Reference9 articles.

1. Puoti G, Bizzi A, Forloni G, et al. Sporadic human prion diseases: molecular insights and diagnosis. Lancet Neurol. 2012;11(7):618–28.

2. Collins SJ, Sanchez-Juan P, Masters CL, et al. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain. 2006;129(pt 9):2278–87.

3. Boesenberg C, et al. Clinical Course in Young Patients with Sporadic Creutzfeldt–Jakob Disease. Ann Neurol. 2005;58:533–43.

4. Diagnostic criteria for sporadic CJD from 1 January 2010. National Creutzfeldt-Jakob Disease Surveillance Diagnostic Criteria [online]. Available from https://www.cdc.gov/prions/cjd/diagnostic-criteria.html .

5. World Health Organization. The Revision of the Surveillance Case Definition for Variant Creutzfeldt-Jakob Disease (vCJD): Report of a WHO consultation, Edinburgh, United Kingdom 17 May 2001. Geneva: World Health Organization; 2002.

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1. KREYTSFELD-YAKOB XƏSTƏLİYİNİN DİAQNOSTİKASININ ÇƏTİNLİKLƏRİ (PRAKTİK MÜŞAHİDƏ);Azerbaijan Medical Journal;2023-03-15

2. Sporadic Creutzfeldt–Jakob Disease in the young (50 and below): 10-year review of United Kingdom surveillance;Journal of Neurology;2022-11-05

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