Fatal familial insomnia: Clinical features and early identification-Reference-Cited by-同舟云学术

Fatal familial insomnia: Clinical features and early identification

Published:2008-05 Issue:5 Volume:63 Page:658-661
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Krasnianski Anna,Bartl Mario,Sanchez Juan Pascual J.,Heinemann Uta,Meissner Bettina,Varges Daniela,Schulze-Sturm Ulf,Kretzschmar Haus A.,Schulz-Schaeffer Walter J.,Zerr Inga

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference20 articles.

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2. Phenotypic variability in familial prion diseases due to the D178N mutation;Zarranz;J Neurol Neurosurg Psychiatry,2005

3. Early age of onset in fatal familial insomnia. Two novel cases and review of the literature;Harder;J Neurol,2004

4. The D178N-129M) “fatal familial insomnia” mutation associated with diverse clinicopathologic phenotypes in an Australian kindred;McLean;Neurology,1997

5. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects;Parchi;Ann Neurol,1999

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