Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy-Reference-Cited by-同舟云学术

Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy

Published:2010-07-01 Issue:1 Volume:121 Page:39-57
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Kovacs Gabor G.,Seguin Jérémie,Quadrio Isabelle,Höftberger Romana,Kapás István,Streichenberger Nathalie,Biacabe Anne Gaëlle,Meyronet David,Sciot Raf,Vandenberghe Rik,Majtenyi Katalin,László Lajos,Ströbel Thomas,Budka Herbert,Perret-Liaudet Armand

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-010-0713-y.pdf

Reference69 articles.

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2. Bertoni JM, Brown P, Goldfarb LG, Rubenstein R, Gajdusek DC (1992) Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy. JAMA 268:2413–2415

3. Braak H, Braak E (1991) Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82:239–259

4. Braak H, Del Tredici K, Rub U, de Vos RA, Jansen Steur EN, Braak E (2003) Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging 24:197–211

5. Brown P, Galvez S, Goldfarb LG, Nieto A, Cartier L, Gibbs CJ Jr, Gajdusek DC (1992) Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20. J Neurol Sci 112:65–67

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