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Showing results 1 to 8 of 8
TypeAuthor(s)TitleOther TitlesCitationCitation(alt)Issue Date
article (author version)Nakamura, Masakazu; Yabe, Ichiro; Yaguchi, Hiroaki; Kishimoto, Riichiro; Mito, Yasunori; Fujiki, Naoto; Houzen, Hideki; Tsuji-Akimoto, Sachiko; Niino, Masaaki; Sasaki, HidenaoClinical characterization and successful treatment of 6 patients with Churg-Strauss syndrome-associated neuropathy-Clinical Neurology and Neurosurgery-Oct-2009
article (author version)Hirotani, Makoto; Niino, Masaaki; Fukazawa, Toshiyuki; Kikuchi, Seiji; Yabe, Ichiro; Hamada, Shinsuke; Tajima, Yasutaka; Sasaki, HidenaoDecreased IL-10 production mediated by Toll-like receptor 9 in B cells in multiple sclerosis-Journal of Neuroimmunology-15-Apr-2010
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, HidenaoDownbeat 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, HidenaoFour mutations of the spastin gene in Japanese families with spastic paraplegia-Journal of Human Genetics-Aug-2006
article (author version)Niino, Masaaki; Hirotani, Makoto; Miyazaki, Yusei; Sasaki, HidenaoMemory and naïve B-cell subsets in patients with multiple sclerosis-Neuroscience Letters-16-Oct-2009
article (author version)Yabe, Ichiro; Soma, Hiroyuki; Takei, Asako; Fujiki, Naoto; Yanagihara, Tetsuro; Sasaki, HidenaoMSA-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, HidenaoSpectrum 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)Basri, Rehana; Yabe, Ichiro; Soma, Hiroyuki; Matsushima, Masaaki; Tsuji, Sachiko; Sasaki, HidenaoX-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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