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Muscle & Nerve|January 17, 2012
Fasciculation potentials in amyotrophic lateral sclerosis and the diagnostic yield of the Awaji algorithmMana Higashihara, Masahiro Sonoo, Ichiro Imafuku, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 6, 2004
[Gene diagnosis of patients with chorea]Takayoshi Shimohata, Osamu Onodera, Yoshiaki Honma, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 20, 2005
[A pedigree of Charcot-Marie-Tooth disease type 4F (Periaxin mutation)]Mitsuteru Shimohata, Kiyoshi Hirahara, Shuichi Igarashi, et al.
Molecular Genetics & Genomic Medicine|December 27, 2019
VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegiaKishin Koh, Hiroyuki Ishiura, Haruo Shimazaki, et al.
Pediatric Research|December 7, 2017
Urinary C-megalin for screening of renal scarring in children after febrile urinary tract infectionSohsaku Yamanouchi, Takahisa Kimata, Jiro Kino, et al.
BMC Pulmonary Medicine|December 9, 2017
The incidence and risk factors of asymptomatic primary spontaneous pneumothorax detected during health check-upsAkihisa Mitani, Yukichika Hakamata, Megumi Hosoi, et al.
Microorganisms|October 28, 2023
Abnormal Development of Microbiota May Be a Risk Factor for Febrile Urinary Tract Infection in InfancyChika Urakami, Sohsaku Yamanouchi, Takahisa Kimata, et al.
Pediatric Research|June 23, 2020
Idiopathic nephrotic syndrome in children: role of regulatory T cells and gut microbiotaShoji Tsuji, Shohei Akagawa, Yuko Akagawa, et al.
The American Journal of Pathology|June 25, 2004
Mostly separate distributions of CLAC- versus Abeta40- or thioflavin S-reactivities in senile plaques reveal two distinct subpopulations of beta-amyloid depositsHisatomo Kowa, Tomoko Sakakura, Yusuke Matsuura, et al.
Neurogenetics|May 22, 2009
Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystoniaKang Wang, Yuji Takahashi, Zong-Liang Gao, et al.
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