An autopsy case of an aged patient with spinocerebellar ataxia type 2-Reference-Cited by-同舟云学术

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An autopsy case of an aged patient with spinocerebellar ataxia type 2

Published:2010-12-06 Issue:5 Volume:31 Page:510-518
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:

Author:

Ishida Chiho,Komai Kiyonobu,Yonezawa Kohei,Sakajiri Ken-ichi,Nitta Eishun,Kawashima Atsuhiro,Yamada Masahito

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1789.2010.01176.x/fullpdf

Reference30 articles.

1. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2;Pulst;Nat Genet,1996

2. Menzel's hereditary ataxia with slow eye movements and myoclonus: a clinico-pathological study;Rondont;J Neurol Sci,1983

3. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families;Dürr;Brain,1995

4. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese;Gwinn-Hardy;Neurology,2000

5. Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2);Furtado;Mov Disord,2004

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1. MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II;Heliyon;2024-04

2. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study;Journal of Neurology, Neurosurgery & Psychiatry;2024-02-21

3. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias;The Cerebellum;2023-03-31

4. Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings;Neuropathology;2022-07-20

5. Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study;Acta Neuropathologica Communications;2021-10-24

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