A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: A clinicopathological study-Reference-Cited by-同舟云学术

A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: A clinicopathological study

Published:1994-12 Issue:1 Volume:127 Page:77-86
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Itoh Yoshinori,Yamada Masahito,Hayakawa Michio,Shozawa Takeshi,Tanaka Jun-ichi,Matsushita Masaaki,Kitamoto Tetsuyuki,Tateishi Jun,Otomo Eiichi

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference44 articles.

1. Familial cerebral amyloidosis and spongiform encephalopathy;Adam;J. Neurol. Neurosurg. Psychiat.,1982

2. Gerstmann-Sträussler syndrome — a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex;Amano;Acta Neuropathol. (Berl.),1992

3. The Mast syndrome: a recessively inherited form of presenile dementia with motor disturbances;Cross;Arch. Neurol.,1967

4. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene;Dlouhy;Nat. Genet.,1992

5. Pro → Leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome;Doh-ura;Biochem. Biophys. Res. Commun.,1989

Cited by 31 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. Serial changes in regional cerebral blood flow in Gerstmann–Sträussler–Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene;Prion;2023-09-13

2. Prion Mutations in Republic of Republic of Korea, China, and Japan;International Journal of Molecular Sciences;2022-12-30

3. Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data;International Journal of Molecular Sciences;2021-12-10

4. Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients;Pathogens;2020-09-28

5. Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene;Prion;2018-11-02