Familial Creutzfeldt-Jakob Disease With an R208H-129V Haplotype and Kuru Plaques-Reference-Cited by-同舟云学术

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Familial Creutzfeldt-Jakob Disease With an R208H-129V Haplotype and Kuru Plaques

Published:2006-03-01 Issue:3 Volume:63 Page:449
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Basset-Leobon Céline,Uro-Coste Emmanuelle,Peoc’h Katell,Haik Stéphane,Sazdovitch Véronique,Rigal Mathieu,Andreoletti Olivier,Hauw Jean-Jacques,Delisle Marie-Bernadette

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 18 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. Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect;neurogenetics;2020-05-26

2. Using NMR spectroscopy to investigate the role played by copper in prion diseases;Neurological Sciences;2020-04-24

3. Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier;Acta Neuropathologica Communications;2019-03-21

4. Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases;Neuropsychiatric Disease and Treatment;2018-08

5. Genetic Creutzfeldt–Jakob disease;Human Prion Diseases;2018

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