Two Cases of Acute Disseminated Encephalomyelitis Following Vaccination Against Human Papilloma Virus

by Sekiguchi, Kenji, Yasui, Naoko, Kowa, Hisatomo, Kanda, Fumio, Toda, Tatsushi
Published 2016

Neuroimaging features of xeroderma pigmentosum group A

by Ueda, Takehiro, Kanda, Fumio, Aoyama, Nobukazu, Fujii, Masahiko, Nishigori, Chikako, Toda, Tatsushi
Published 2012

Disease-associated marked hyperalphalipoproteinemia

by Hirano, Ken-ichi, Nagasaka, Hironori, Kobayashi, Kazuhiro, Yamaguchi, Satoshi, Suzuki, Akira, Toda, Tatsushi, Doyu, Manabu
Published 2014

Contribution of Dysferlin Deficiency to Skeletal Muscle Pathology in Asymptomatic and Severe Dystroglycanopathy Models: Generation of a New Model for Fukuyama Congenital Muscular D...

by Kanagawa, Motoi, Lu, Zhongpeng, Ito, Chiyomi, Matsuda, Chie, Miyake, Katsuya, Toda, Tatsushi
Published 2014

Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression

by Ohtsuka, Yoshihisa, Kanagawa, Motoi, Yu, Chih-Chieh, Ito, Chiyomi, Chiyo, Tomoko, Kobayashi, Kazuhiro, Okada, Takashi, Takeda, Shin'ichi, Toda, Tatsushi
Published 2015

The Aggregation Inhibitor Peptide QBP1 as a Therapeutic Molecule for the Polyglutamine Neurodegenerative Diseases

by Popiel, H. Akiko, Burke, James R., Strittmatter, Warren J., Oishi, Shinya, Fujii, Nobutaka, Takeuchi, Toshihide, Toda, Tatsushi, Wada, Keiji, Nagai, Yoshitaka
Published 2011

Plasmablasts as Migratory IgG-Producing Cells in the Pathogenesis of Neuromyelitis Optica

by Chihara, Norio, Aranami, Toshimasa, Oki, Shinji, Matsuoka, Takako, Nakamura, Masakazu, Kishida, Hitaru, Yokoyama, Kazumasa, Kuroiwa, Yoshiyuki, Hattori, Nobutaka, Okamoto, Tomoko, Murata, Miho, Toda, Tatsushi, Miyake, Sachiko, Yamamura, Takashi
Published 2013

AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan

by Yagi, Hirokazu, Nakagawa, Naoki, Saito, Takuya, Kiyonari, Hiroshi, Abe, Takaya, Toda, Tatsushi, Wu, Sz-Wei, Khoo, Kay-Hooi, Oka, Shogo, Kato, Koichi
Published 2013

Hsp40 Gene Therapy Exerts Therapeutic Effects on Polyglutamine Disease Mice via a Non-Cell Autonomous Mechanism

by Popiel, H. Akiko, Takeuchi, Toshihide, Fujita, Hiromi, Yamamoto, Kazuhiro, Ito, Chiyomi, Yamane, Hiroshi, Muramatsu, Shin-ichi, Toda, Tatsushi, Wada, Keiji, Nagai, Yoshitaka
Published 2012

Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels

by Yu, Chih-Chieh, Furukawa, Mari, Kobayashi, Kazuhiro, Shikishima, Chizuru, Cha, Pei-Chieng, Sese, Jun, Sugawara, Hiroko, Iwamoto, Kazuya, Kato, Tadafumi, Ando, Juko, Toda, Tatsushi
Published 2012

TRPV2 is critical for the maintenance of cardiac structure and function in mice

by Katanosaka, Yuki, Iwasaki, Keiichiro, Ujihara, Yoshihiro, Takatsu, Satomi, Nishitsuji, Koki, Kanagawa, Motoi, Sudo, Atsushi, Toda, Tatsushi, Katanosaka, Kimiaki, Mohri, Satoshi, Naruse, Keiji
Published 2014

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

by Shigemizu, Daichi, Aiba, Takeshi, Nakagawa, Hidewaki, Ozaki, Kouichi, Miya, Fuyuki, Satake, Wataru, Toda, Tatsushi, Miyamoto, Yoshihiro, Fujimoto, Akihiro, Suzuki, Yutaka, Kubo, Michiaki, Tsunoda, Tatsuhiko, Shimizu, Wataru, Tanaka, Toshihiro
Published 2015

Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy

by Taniguchi-Ikeda, Mariko, Kobayashi, Kazuhiro, Kanagawa, Motoi, Yu, Chih-chieh, Mori, Kouhei, Oda, Tetsuya, Kuga, Atsushi, Kurahashi, Hiroki, Akman, Hasan O., DiMauro, Salvatore, Kaji, Ryuji, Yokota, Toshifumi, Takeda, Shin’ichi, Toda, Tatsushi
Published 2011

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan

by Hirano, Makito, Satake, Wataru, Ihara, Kenji, Tsuge, Ikuya, Kondo, Shuji, Saida, Ken, Betsui, Hiroyuki, Okubo, Kazuhiro, Sakamoto, Hikaru, Ueno, Shuichi, Ikuno, Yasushi, Ishihara, Ryu, Iwahashi, Hiromi, Ohishi, Mitsuru, Mano, Toshiyuki, Yamashita, Toshihide, Suzuki, Yutaka, Nakamura, Yusaku, Kusunoki, Susumu, Toda, Tatsushi
Published 2015

Peripheral leukocyte anomaly detected with routine automated hematology analyzer sensitive to adipose triglyceride lipase deficiency manifesting neutral lipid storage disease with...

by Suzuki, Akira, Nagasaka, Hironori, Ochi, Yasuhiro, Kobayashi, Kazuhiro, Nakamura, Hiroshi, Nakatani, Daisaku, Yamaguchi, Satoshi, Yamaki, Shinobu, Wada, Atsushi, Shirata, Yoshihisa, Hui, Shu-Ping, Toda, Tatsushi, Kuroda, Hiroshi, Chiba, Hitoshi, Hirano, Ken-ichi
Published 2014

A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy

by Oda, Tetsuya, Xiong, Hui, Kobayashi, Kazuhiro, Wang, Shuo, Satake, Wataru, Jiao, Hui, Yang, Yanling, Cha, Pei-Chieng, Hayashi, Yukiko K, Nishino, Ichizo, Suzuki, Yutaka, Sugano, Sumio, Wu, Xiru, Toda, Tatsushi
Published 2015

Prenatal genetic testing for familial severe congenital protein C deficiency

by Tairaku, Shinya, Taniguchi-Ikeda, Mariko, Okazaki, Yoko, Noguchi, Yoriko, Nakamachi, Yuji, Mori, Takeshi, Kubokawa, Ikuko, Hayakawa, Akira, Shibata, Akio, Emoto, Tomomi, Kurahashi, Hiroki, Toda, Tatsushi, Kawano, Seiji, Yamada, Hideto, Morioka, Ichiro, Iijima, Kazumoto
Published 2015

ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout

by Matsuo, Hirotaka, Tomiyama, Hiroyuki, Satake, Wataru, Chiba, Toshinori, Onoue, Hiroyuki, Kawamura, Yusuke, Nakayama, Akiyoshi, Shimizu, Seiko, Sakiyama, Masayuki, Funayama, Manabu, Nishioka, Kenya, Shimizu, Toru, Kaida, Kenichi, Kamakura, Keiko, Toda, Tatsushi, Hattori, Nobutaka, Shinomiya, Nariyoshi
Published 2015

Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex

by Nagata, Eiko, Kano, Hiroki, Kato, Fumiko, Yamaguchi, Rie, Nakashima, Shinichi, Takayama, Shinichiro, Kosaki, Rika, Tonoki, Hidefumi, Mizuno, Seiji, Watanabe, Satoshi, Yoshiura, Koh-ichiro, Kosho, Tomoki, Hasegawa, Tomonobu, Kimizuka, Mamori, Suzuki, Atsushi, Shimizu, Kenji, Ohashi, Hirofumi, Haga, Nobuhiko, Numabe, Hironao, Horii, Emiko, Nagai, Toshiro, Yoshihashi, Hiroshi, Nishimura, Gen, Toda, Tatsushi, Takada, Shuji, Yokoyama, Shigetoshi, Asahara, Hiroshi, Sano, Shinichiro, Fukami, Maki, Ikegawa, Shiro, Ogata, Tsutomu
Published 2014

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

by Lill, Christina M., Roehr, Johannes T., McQueen, Matthew B., Kavvoura, Fotini K., Bagade, Sachin, Schjeide, Brit-Maren M., Schjeide, Leif M., Meissner, Esther, Zauft, Ute, Allen, Nicole C., Liu, Tian, Schilling, Marcel, Anderson, Kari J., Beecham, Gary, Berg, Daniela, Biernacka, Joanna M., Brice, Alexis, DeStefano, Anita L., Do, Chuong B., Eriksson, Nicholas, Factor, Stewart A., Farrer, Matthew J., Foroud, Tatiana, Gasser, Thomas, Hamza, Taye, Hardy, John A., Heutink, Peter, Hill-Burns, Erin M., Klein, Christine, Latourelle, Jeanne C., Maraganore, Demetrius M., Martin, Eden R., Martinez, Maria, Myers, Richard H., Nalls, Michael A., Pankratz, Nathan, Payami, Haydeh, Satake, Wataru, Scott, William K., Sharma, Manu, Singleton, Andrew B., Stefansson, Kari, Toda, Tatsushi, Tung, Joyce Y., Vance, Jeffery, Wood, Nick W., Zabetian, Cyrus P., Young, Peter, Tanzi, Rudolph E., Khoury, Muin J., Zipp, Frauke, Lehrach, Hans, Ioannidis, John P. A., Bertram, Lars
Published 2012