Congenital myotonic dystrophy can show congenital fiber type disproportion pathology
Tominaga, Kayo, Hayashi, Yukiko K., Goto, Kanako, Minami, Narihiro, Noguchi, Satoru, Nonaka, Ikuya, Miki, Tetsuro, Nishino, Ichizo
Published in Acta neuropathologica (01.04.2010)
Published in Acta neuropathologica (01.04.2010)
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Journal Article
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
Hayashi, Yukiko K, Matsuda, Chie, Ogawa, Megumu, Goto, Kanako, Tominaga, Kayo, Mitsuhashi, Satomi, Park, Young-Eun, Nonaka, Ikuya, Hino-Fukuyo, Naomi, Haginoya, Kazuhiro, Sugano, Hisashi, Nishino, Ichizo
Published in The Journal of clinical investigation (01.09.2009)
Published in The Journal of clinical investigation (01.09.2009)
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Journal Article
Case of Hashimoto's encephalopathy with diffuse white matter lesions on diffusion-weighted MRI
Okamoto, Kensho, Mori, Chiaki, Kamogawa, Kenji, Tominaga, Kayo, Okuda, Bungo
Published in Rinshō shinkeigaku (01.02.2007)
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Published in Rinshō shinkeigaku (01.02.2007)
Journal Article
A clinicoanatomical study of thalamic cheiro-oral syndrome
Kamogawa, Kenji, Tominaga, Kayo, Okamoto, Kensho, Okuda, Bungo
Published in Nihon Rōnen Igakkai zasshi (2006)
Published in Nihon Rōnen Igakkai zasshi (2006)
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Journal Article
A novel photointermediate of octopus rhodopsin activates its G-protein
Nakagawa, Masashi, Kikkawa, Satoshi, Tominaga, Kayo, Tsugi, Naoko, Tsuda, Motoyuki
Published in FEBS letters (02.10.1998)
Published in FEBS letters (02.10.1998)
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Journal Article
Multifocal enhancing cortical lesions in a patient with Churg-Strauss syndrome
Hagiwara, Koichi, Tominaga, Kayo, Shida, Norihiko, Yamashita, Yoriaki
Published in Neurology (04.11.2008)
Published in Neurology (04.11.2008)
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Journal Article
Family with centronuclear myopathy as a result of a novel p.R369G DNM 2 mutation
Toyooka, Keiko, Kubo, Kumiko, Fujimura, Harutoshi, Sakoda, Sabro, Tominaga, Kayo, Nishino, Ichizo
Published in Neurology and clinical neuroscience (01.07.2015)
Published in Neurology and clinical neuroscience (01.07.2015)
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Journal Article
Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations
Saito, Yoshiaki, Komaki, Hirofumi, Hattori, Ayako, Takeuchi, Fumi, Sasaki, Masayuki, Kawabata, Ken, Mitsuhashi, Satomi, Tominaga, Kayo, Hayashi, Yukiko K, Nowak, Kristen J, Laing, Nigel G, Nonaka, Ikuya, Nishino, Ichizo
Published in Neuromuscular disorders : NMD (01.07.2011)
Published in Neuromuscular disorders : NMD (01.07.2011)
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Journal Article
Family with centronuclear myopathy as a result of a novel p.R369G DNM2 mutation
Toyooka, Keiko, Kubo, Kumiko, Fujimura, Harutoshi, Sakoda, Sabro, Tominaga, Kayo, Nishino, Ichizo
Published in Neurology and clinical neuroscience (01.07.2015)
Published in Neurology and clinical neuroscience (01.07.2015)
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Journal Article