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Experimental Neurology|March 6, 2003
The efficacy of trientine or ascorbate alone compared to that of the combined treatment with these two agents in familial amyotrophic lateral sclerosis model miceSeiichi Nagano, Yuuichi Fujii, Takeshi Yamamoto, et al.The Journal of Biological Chemistry|April 4, 2007
Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complexFujian Zhang, Anna-Lena Ström, Kei Fukada, et al.Journal of the Neurological Sciences|February 5, 2004
Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analysesTakako Sato, Yoichi Yamamoto, Toyofumi Nakanishi, et al.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|March 9, 2017
Postural flexibility during quiet standing in healthy elderly and patients with Parkinson's diseaseKazuyuki Matsuda, Yasuyuki Suzuki, Naoya Yoshikawa, et al.Journal of the Neurological Sciences|December 17, 2013
Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxiaRyosuke Miyamoto, Hiroyuki Morino, Akio Yoshizawa, et al.Acta Neuropathologica|October 1, 2003
Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese familiesTakayo Arisato, Ryuichi Okubo, Hitoshi Arata, et al.Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|June 14, 2016
The Motor Unit Number Index of Subclinical Abnormality in Amyotrophic Lateral SclerosisKei Fukada, Toyoko Matsui, Mitsuru Furuta, et al.Pageof 2