Unusual presentations in patients with E200K familial Creutzfeldt−Jakob disease-Reference-Cited by-同舟云学术

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Unusual presentations in patients with E200K familial Creutzfeldt−Jakob disease

Published:2016-01-25 Issue:5 Volume:23 Page:871-877
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Cohen O. S.¹²³,Kimiagar I.²³,Korczyn A. D.³,Nitsan Z.⁴,Appel S.⁴,Hoffmann C.⁵,Rosenmann H.⁶,Kahana E.⁴,Chapman J.¹³

Affiliation:

1. Department of Neurology; Chaim Sheba Medical Center; Tel-Hashomer Israel

2. Department of Neurology; Assaf Harofeh Medical Center; Zerifin Israel

3. Sackler Faculty of Medicine; Tel-Aviv University; Tel-Aviv Israel

4. Barzilai Medical Center; Ashkelon Israel

5. Department of Radiology; Chaim Sheba Medical Center; Tel-Hashomer Israel

6. Department of Neurology; Hadassah Hebrew University Medical Center; Jerusalem Israel

Funder

National Institutes of Health

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12955/fullpdf

Reference49 articles.

1. Molecular biology of prion diseases;Prusiner;Science,1991

2. Prion diseases;Knight;J Neurol Neurosurg Psychiatry,2004

3. Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt−Jakob disease in Sephardic Jews of Libyan and non-Libyan origin;Goldfarb;Lancet,1990

4. The risk of developing Creutzfeldt−Jakob disease in subjects with the PRNP gene codon 200 point mutation;Chapman;Neurology,1994

5. Creutzfeldt−Jakob disease among Libyan Jews;Korczyn;Eur J Epidemiol,1991

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4. Case 5-2022: A 65-Year-Old Woman with Rapidly Progressive Weakness in the Right Arm and Recurrent Falls;New England Journal of Medicine;2022-02-17

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