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Showing results 1 to 6 of 6
TypeAuthor(s)TitleOther TitlesCitationCitation(alt)Issue Date
article (author version)Sakushima, Ken; Tsuji-Akimoto, Sachiko; Niino, Masaaki; Saitoh, Shinji; Yabe, Ichiro; Sasaki, HidenaoAdult Leigh Disease Without Failure to Thrive-Neurologist-Jul-2011
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)Sato, Kazunori; Yabe, Ichiro; Yaguchi, Hiroaki; Nakano, Fumihito; Kunieda, Yasuyuki; Saitoh, Shinji; Sasaki, HidenaoGenetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism.-Journal of neurology-Jul-2011
article (author version)Asahina, Naoko; Okamoto, Takayuki; Sudo, Akira; Kanazawa, Naomi; Tsujino, Seiichi; Saitoh, ShinjiAn infantile/juvenile form of Alexander disease caused by a R79H mutation in GFAP-Brain and Development-Mar-2006
article (author version)Nakamura, Masakazu; Yabe, Ichiro; Sudo, Akira; Hosoki, Kana; Yaguchi, Hiroaki; Saitoh, Shinji; Sasaki, HidenaoMERRF/MELAS overlap syndrome: A double pathogenic mutation in mitochondrial tRNA genes-Journal of Medical Genetics-7-Jul-2010
articleSudo, A.; Takeichi, N.; Hosoki, K.; Saitoh, S.Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G > A transition-Journal of Laryngology & Otology-Dec-2011
Showing results 1 to 6 of 6

 

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