An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1mutation-Reference-Cited by-同舟云学术

An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1mutation

Published:2013-06-17 Issue:1 Volume:34 Page:58-63
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Nakamura Seika¹,Wate Reika¹,Kaneko Satoshi¹,Ito Hidefumi²,Oki Mitsuaki¹,Tsuge Ayako¹,Nagashima Masato¹,Asayama Shinya¹,Fujita Kengo¹,Nakamura Masataka¹,Maruyama Hirofumi³,Kawakami Hideshi³,Kusaka Hirofumi¹

Affiliation:

1. Department of Neurology; Kansai Medical University; Hirakata Japan

2. Department of Neurology; Wakayama Medical University; Wakayama Japan

3. Department of Epidemiology; Research Institute for Radiation Biology and Medicine; Hiroshima University; Hiroshima Japan

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12049/fullpdf

Reference24 articles.

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3. Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells;Hirano;Arch Neurol,1967

4. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase;Deng;Science,1993

5. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene;Cudkowicz;Ann Neurol,1998

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