Hereditary progressive dystonia with marked diurnal fluctuation von Segawa, Masaya

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Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease) von Segawa, Masaya, Nomura, Yoshiko, Nishiyama, Nobuyoshi

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Early motor disturbances in Rett syndrome and its pathophysiological importance von Segawa, Masaya

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Epilepsy in autism: A pathophysiological consideration von Nomura, Yoshiko, Nagao, Yuri, Kimura, Kazue, Hachimori, Kei, Segawa, Masaya

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Deterioration of horizontal saccades in progressive supranuclear palsy von Terao, Yasuo, Fukuda, Hideki, Shirota, Yuichiro, Yugeta, Akihiro, Yoshioka, Masayuki, Suzuki, Masahiko, Hanajima, Ritsuko, Nomura, Yoshiko, Segawa, Masaya, Tsuji, Shoji, Ugawa, Yoshikazu

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Pre-movement gating of somatosensory evoked potentials in Segawa disease von Kimura, Kazue, Nagao, Yuri, Hachimori, Kei, Hayashi, Masaharu, Nomura, Yoshiko, Segawa, Masaya

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy von Kobayashi, Kazuhiro, Nakahori, Yutaka, Miyake, Masashi, Matsumura, Kiichiro, Kondo-Iida, Eri, Nomura, Yoshiko, Segawa, Masaya, Yoshioka, Mieko, Saito, Kayoko, Osawa, Makiko, Hamano, Kenzo, Sakakihara, Youichi, Nonaka, Ikuya, Nakagome, Yasuo, Kanazawa, Ichiro, Nakamura, Yusuke, Tokunaga, Katsushi, Toda, Tatsushi

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Hereditary progressive dystonia with marked diurnal fluctuation von Segawa, Masaya

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Epochs of development of the sleep-wake cycle reflect the modulation of the higher cortical function particular for each epoch von SEGAWA, Masaya

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Methyl CpG-Binding Protein 2 (a Mutation of Which Causes Rett Syndrome) Directly Regulates Insulin-Like Growth Factor Binding Protein 3 in Mouse and Human Brains von Itoh, Masayuki, Ide, Shuhei, Takashima, Sachio, Kudo, Shinichi, Nomura, Yoshiko, Segawa, Masaya, Kubota, Takeo, Mori, Hideo, Tanaka, Shigeki, Horie, Hiroshi, Tanabe, Yuzo, Goto, Yu-ichi

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Natural History of Rett Syndrome von Nomura, Yoshiko, Segawa, Masaya

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Neurophysiology of Tourette's syndrome: pathophysiological considerations von Segawa, Masaya

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Development of the nigrostriatal dopamine neuron and the pathways in the basal ganglia von Segawa, Masaya

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Cases of dopa-responsive dystonia (Segawa disease) in Estonia von Talvik, Inga, Segawa, Masaya, Veri, Kadi, Gross-Paju, Katrin, Talvik, Tiina

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Dopa-responsive dystonia von Segawa, Masaya

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O1-E-25. The effect of obsessive compulsive disorder on saccade performance in Gilles de la Tourette (GTS) syndrome von Terao, Yasuo, Fukuda, Hideki, Hachimori, Kei, Kimura, Kazue, Matsumoto, Misako, Matsuda, Shunnichi, Yugeta, Akihiro, Hanajima, Ritsuko, Ugawa, Yoshikazu, Nomura, Yoshiko, Segawa, Masaya

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Discussant – pathophysiologies of Rett syndrome von Segawa, Masaya

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Pathophysiology of Rett syndrome from the stand point of clinical characteristics von Segawa, Masaya

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A variant of childhood-onset myasthenia gravis: HLA typing and clinical characteristics in Japan von Shinomiya, Noriaki, Nomura, Yoshiko, Segawa, Masaya

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Guidelines for reporting clinical features in cases with MECP2 mutations von Kerr, Alison M., Nomura, Yoshiko, Armstrong, Dawna, Anvret, Maria, Belichenko, Pavel V., Budden, Sarojini, Cass, Hilary, Christodoulou, John, Clarke, Angus, Ellaway, Carolyn, d'Esposito, Maurizio, Francke, Uta, Hulten, Maj, Julu, Peter, Leonard, Helen, Naidu, Sakkubai, Schanen, Carolyn, Webb, Tessa, Engerstrom, Ingegerd Witt, Yamashita, Yushiro, Segawa, Masaya

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