Familial spongiform encephalopathy associated with a novel prion protein gene mutation-Reference-Cited by-同舟云学术

Familial spongiform encephalopathy associated with a novel prion protein gene mutation

Published:1997-08 Issue:2 Volume:42 Page:138-146
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Nitrini Ricardo,Rosemberg Sergio,Passos-Bueno Maria Rita,da Silva Lu�s S. Teixeira,Iughetti Paula,Papadopoulos Maria,Carrilho Paulo M.,Caramelli Paulo,Albrecht Steffen,Zatz Mayana,LeBlanc Andrea

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference40 articles.

1. Inherited prion diseases.

2. Inherited Prion Diseases and Transmission to Rodents

3. The Nosology of Creutzfeldt-Jakob Disease and Conditions Related to the Accumulation of PrPCJDin the Nervous System

4. Unconventional Viruses and the Origin and Disappearance of Kuru

5. Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

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