Characterization of sleep disorders in patients with E200K familial Creutzfeldt

Characterization of sleep disorders in patients with E200K familial Creutzfeldt–Jakob disease

Published:2014-12-02 Issue:2 Volume:262 Page:443-450
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Cohen Oren S.,Chapman Joab,Korczyn Amos D.,Warman-Alaluf Naama,Orlev Yael,Givaty Gili,Nitsan Zeev,Appel Shmuel,Rosenmann Hanna,Kahana Esther,Shechter-Amir Dalia

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-014-7593-3.pdf

Reference26 articles.

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4. Goldfarb LG, Korczyn AD, Brown P, Chapman J, Gajdusek DC (1990) Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt–Jakob disease in Sephardic Jews of Libyan and non-Libyan origin. Lancet 336:637–638

5. Hsiao K, Meiner Z, Kahana E, Cass C, Kahana I, Avrahami D, Scarlato G, Abramsky O, Prusiner SB, Gabizon R (1991) Mutation of the prion protein in Libyan Jews with Creutzfeldt–Jakob disease. N Engl J Med 324:1091–1097

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