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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 15, 2014 - Issue 3-4
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Brief Report

Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene

Hikaru SakamotoDepartment of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Osaka, Japan
,
Maiko AkamatsuDepartment of Neurology, Kongo Hospital, Osaka, Japan
,
Makito HiranoDepartment of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Osaka, Japan;Department of Neurology, Kinki University Faculty of Medicine, Osaka, JapanCorrespondence[email protected]
,
Kazumasa SaigohDepartment of Neurology, Kinki University Faculty of Medicine, Osaka, Japan
,
Shuichi UenoDepartment of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Osaka, Japan
,
Chiharu IsonoDepartment of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Osaka, Japan
,
Susumu KusunokiDepartment of Neurology, Kinki University Faculty of Medicine, Osaka, Japan
&
Yusaku NakamuraDepartment of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Osaka, Japan
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Pages 312-314 | Received 29 Sep 2013, Accepted 03 Dec 2013, Published online: 10 Mar 2014

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Yudhiakuari Sincihu, Muhammad Farid Dimjadi Lusno, Tri Marthy Mulyasari, Saliza Mohd Elias, I Ketut Sudiana, Kurnia Kusumastuti, Lilis Sulistyorini & Soedjajadi Keman. (2023) Wistar Rats Hippocampal Neurons Response to Blood Low-Density Polyethylene Microplastics: A Pathway Analysis of SOD, CAT, MDA, 8-OHdG Expression in Hippocampal Neurons and Blood Serum Aβ42 Levels. Neuropsychiatric Disease and Treatment 19, pages 73-83.
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P. A. McCombe, N. R. Wray & R. D. Henderson. (2017) Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity. Expert Review of Neurotherapeutics 17:6, pages 561-577.
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Articles from other publishers (6)

Pan Liu, Yongxiang Tang, Wanzhen Li, Zhen Liu, Ming Zhou, Jian Li, Yanchun Yuan, Liangjuan Fang, Jifeng Guo, Lu Shen, Hong Jiang, Beisha Tang, Shuo Hu & Junling Wang. (2023) Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis. CNS Neuroscience & Therapeutics 29:9, pages 2530-2539.
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Cheng Chang, Qianqian Zhao, Pan Liu, Yanchun Yuan, Zhen Liu, Yiting Hu, Wanzhen Li, Xiaorong Hou, Xuxiong Tang, Bin Jiao, Jifeng Guo, Lu Shen, Hong Jiang, Beisha Tang, Xuewei Zhang & Junling Wang. (2023) ALS-plus related clinical and genetic study from China. Neurological Sciences.
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Qing-Qing Tao, Qiao Wei & Zhi-Ying Wu. (2018) Sensory nerve disturbance in amyotrophic lateral sclerosis. Life Sciences 203, pages 242-245.
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Kentaro Hayashi, Yoko Mochizuki, Reiji Koide, Akihiro Kawata, Taku Homma, Toshio Shimizu, Takashi Komori & Eiji Isozaki. (2016) A Japanese familial ALS patient with autonomic failure and a p.Cys146Arg mutation in the gene for SOD1 ( SOD1 ) . Neuropathology 36:6, pages 551-555.
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Xinglong Yang, Jing Xi, Ran An, Lihua Yu, Zhenfang Lin, Huayong Zhou & Yanming Xu. (2015) Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population. Neurological Sciences 36:7, pages 1211-1215.
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Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Chiharu Isono, Yoshiyuki Mitsui & Susumu Kusunoki. (2015) VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation. Neurobiology of Aging 36:3, pages 1604.e1-1604.e6.
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