Mitsuteru Shimohata

Multiplex Families With Multiple System Atrophy

Kenju Hara, Yoshio Momose, S. Tokiguchi et al. · Archives of Neurology · 2007 · 141 citations

Life Sciences, Genetics, Neurology +17

SCA17 homozygote showing Huntington's disease‐like phenotype

Yasuko Toyoshima, Mitsunori Yamada, Osamu Onodera et al. · Annals of Neurology · 2004 · 129 citations

Life Sciences, Genetics, Molecular Genetics +16

Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease

Kazuki Kijima, Chikahiko Numakura, Emi Shirahata et al. · Journal of Human Genetics · 2004 · 57 citations

Life Sciences, Genetics, Molecular Medicine +4

Interference of CREB‐dependent transcriptional activation by expanded polyglutamine stretches – augmentation of transcriptional activation as a potential therapeutic strategy for polyglutamine diseases

Mitsuteru Shimohata, Takayoshi Shimohata, S. Igarashi et al. · Journal of Neurochemistry · 2005 · 21 citations

Life Sciences, Molecular Biology, Pharmacology +16

Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease

Tesshu Otagiri, Kenji Sugai, Kazuki Kijima et al. · Journal of Human Genetics · 2006 · 19 citations

Life Sciences, Genetics, Molecular Medicine +4