Showing results (11-20 of 24) with videos related to
Sort By:
Pageof 3
Human Molecular Genetics|March 27, 2004
Aprataxin, a novel protein that protects against genotoxic stressNuri Gueven, Olivier J Becherel, Amanda W Kijas, et al.Archives of Neurology|May 13, 2009
Mutations for Gaucher disease confer high susceptibility to Parkinson diseaseJun Mitsui, Ikuko Mizuta, Atsushi Toyoda, et al.Annals of Neurology|September 27, 2002
A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigreesAki Arai, Keiko Tanaka, Takeshi Ikeuchi, et al.Archives of Neurology|May 29, 2012
C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of JapanHiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, et al.Annals of Neurology|January 22, 2022
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body MyositisChiseko Ikenaga, Hidetoshi Date, Motoi Kanagawa, et al.Brain : a Journal of Neurology|April 14, 2011
Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemiaAkio Yokoseki, Tomohiko Ishihara, Akihide Koyama, et al.Neurobiology of Aging|October 17, 2017
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.American Journal of Human Genetics|August 14, 2012
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementHiroyuki Ishiura, Wataru Sako, Mari Yoshida, et al.American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.Neurology|June 26, 2016
Anti-TIF1-γ antibody and cancer-associated myositis: A clinicohistopathologic studyAyumi Hida, Takenari Yamashita, Yuji Hosono, et al.Pageof 3