Browsing by Author Takahashi, Yuji

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Issue DateTitleAuthor(s)Citation
2013ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Blair, Ian; Fifita, Jennifer; Nicholson, Garth; Williams, Kelly; Belzil, Veronique; Dion, Patrick; Doi, Koichiro; et al, Various; Fukuda, Yoko; Higasa, Koichiro; Kurppa, Kari; Moritoyo, Hiroyoko; Takahashi, Yuji; Toyoda, Atsushi; Yoshimura, Jun; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19, American Journal of Human Genetics, vol.93, 5, 2013,pp 900-905
2013Mutations in COQ2 in Familial and Sporadic Multiple-System AtrophyNicholson, Garth; Ahsan, Budrul; Date, Hidetoshi; et al, Various; Fukuda, Yoko; Ichikawa, Yaeko; Ishiura, Hiroyuki; Matsukawa, Takashi; Mitsui, Jun; Momose, Yoshio; Nakahara, Yasuo; Takahashi, Yuji; Concord Clinical School: ANZAC Research InstituteMutations in COQ2 in Familial and Sporadic Multiple-System Atrophy, New England Journal of Medicine, vol.369, 3, 2013,pp 233-244
2012The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementNicholson, Garth; Ahsan, Budrul; Date, Hidetoshi; et, al; Goto, Jun; Ishiura, Hiroyuki; Kawarai, Toshitaka; Mitsui, Jun; Sako, Wataru; Takahashi, Yuji; Tanabe, Osamu; Yoshida, Mari; Concord Clinical School: ANZAC Research InstituteThe TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement, American Journal of Human Genetics, vol.91, 2, 2012,pp 320-329