A Second Case of Gerstmann-Sträussler-Scheinker Disease Linked to the G131V Mutation in the Prion Protein Gene in a Dutch Patient-Reference-Cited by-同舟云学术

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A Second Case of Gerstmann-Sträussler-Scheinker Disease Linked to the G131V Mutation in the Prion Protein Gene in a Dutch Patient

Published:2011-08 Issue:8 Volume:70 Page:698-702
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:J Neuropathol Exp Neurol

Author:

Jansen Casper,Parchi Piero,Capellari Sabina,Strammiello Rosaria,Dopper Elise G.P.,van Swieten John C.,Kamphorst Wouter,Rozemuller Annemieke J.M.

Publisher

Oxford University Press (OUP)

Subject

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

Reference22 articles.

1. Nobel Lecture: Prions

2. Hereditary prion protein amyloidoses

3. Sporadic and familial CJD: classification and characterisation

4. A New PRNP Mutation (G131V) Associated With Gerstmann-Sträussler-Scheinker Disease

5. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gerstmann‐Sträussler‐Scheinker Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology;Movement Disorders Clinical Practice;2024-01-23

2. Alterations of Striatal Subregions in a Prion Protein Gene V180I Mutation Carrier Presented as Frontotemporal Dementia With Parkinsonism;Frontiers in Aging Neuroscience;2022-04-15

3. An unusual familial dementia associated with G131V PRNP mutation;European Journal of Neurology;2020-10-18

4. Structural effects of the highly protective V127 polymorphism on human prion protein;Communications Biology;2020-07-29

5. A novel PRNP-G131R variant associated with familial prion disease;Neurology Genetics;2020-06-05

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