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Hokkaido University Collection of Scholarly and Academic Papers >
Showing results 1 to 8 of 8
Type | Author(s) | Title | Other Titles | Citation | Citation(alt) | Issue Date | article (author version) | Yabe, Ichiro; Kitagawa, Mayumi; Suzuki, Yashio; Fujiwara, Keishi; Wada, Takahito; Tsubuku, Takashi; Takeichi, Norihito; Sakushima, Ken; Soma, Hiroyuki; Tsuji, Sachiko; Niino, Masaaki; Saitoh, Shinji; Sasaki, Hidenao | Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family | - | Journal of Neurology | - | Oct-2008 |
article (author version) | Basri, Rehana; Yabe, Ichiro; Soma, Hiroyuki; Takei, Asako; Nishimura, Hiroyuki; Machino, Yuka; Kokubo, Yasumasa; Kosugi, Masafumi; Okada, Ryuichirou; Yukitake, Motohiro; Tachibana, Hisao; Kuroda, Yasuo; Kuzuhara, Shigeki; Sasaki, Hidenao | Four mutations of the spastin gene in Japanese families with spastic paraplegia | - | Journal of Human Genetics | - | Aug-2006 |
article (author version) | Soma, Hiroyuki; Yabe, Ichiro; Takei, Asako; Fujiki, Naoto; Yanagihara, Tetsuro; Sasaki, Hidenao | Heredity in Multiple System Atrophy | - | Journal of the Neurological Sciences | - | 15-Jan-2006 |
article | Tha, Khin K; Terae, Satoshi; Tsukahara, Akiko; Soma, Hiroyuki; Morita, Ryo; Yabe, Ichiro; Ito, Yoichi M; Sasaki, Hidenao; Shirato, Hiroki | Hyperintense putaminal rim at 1.5 T: prevalence in normal subjects and distinguishing features from multiple system atrophy | - | BMC Neurology | - | 18-Jun-2012 |
article (author version) | Yabe, Ichiro; Soma, Hiroyuki; Takei, Asako; Fujiki, Naoto; Yanagihara, Tetsuro; Sasaki, Hidenao | MSA-C is the predominant clinical phenotype of MSA in Japan : Analysis of 142 patients with probable MSA | - | Journal of the Neurological Sciences | - | 15-Nov-2006 |
article (author version) | Basri, Rehana; Yabe, Ichiro; Soma, Hiroyuki; Sasaki, Hidenao | Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan : a study of 113 Japanese families | - | Journal of Human Genetics | - | Oct-2007 |
article (author version) | Inaba, Hirofumi; Yabe, Ichiro; Yashima, Moemi; Soma, Hiroyuki; Nakamura, Yasushi; Houzen, Hideki; Sasaki, Hidenao | Unusual Retinal Phenotypes in an SCA7 Family | - | Internal Medicine | - | 17-Aug-2009 |
article (author version) | Basri, Rehana; Yabe, Ichiro; Soma, Hiroyuki; Matsushima, Masaaki; Tsuji, Sachiko; Sasaki, Hidenao | X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter | - | Internal Medicine | - | 2007 |
Showing results 1 to 8 of 8
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