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Internal Medicine (Tokyo, Japan)|December 4, 2015
Anti-Hu Antibody-associated Paraneoplastic Neurological Syndrome Showing Peripheral Neuropathy and Atypical Multifocal Brain LesionsMakoto Shibata, Megumi Uchida, Setsuki Tsukagoshi, et al.Brain Research|August 11, 2007
Increased autophagy in transgenic mice with a G93A mutant SOD1 geneNobutoshi Morimoto, Makiko Nagai, Yasuyuki Ohta, et al.Neurological Research|May 4, 2011
Comparisons of acoustic function in SCA31 and other forms of ataxiasYoshio Ikeda, Makiko Nagai, Tomoko Kurata, et al.Journal of the Neurological Sciences|March 3, 2015
Simultaneous assessment of cognitive and affective functions in multiple system atrophy and cortical cerebellar atrophy in relation to computerized touch-panel screening testsYuko Kawahara, Yoshio Ikeda, Kentaro Deguchi, et al.Brain Research|April 27, 2010
Temporal and spatial differences of multiple protein expression in the ischemic penumbra after transient MCAO in ratsXuemei Zhang, Kentaro Deguchi, Toru Yamashita, et al.Journal of the Neurological Sciences|July 13, 2010
A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: a clinical, pathological and genetic reportYukiko Yamamoto-Watanabe, Mitsunori Watanabe, Koichi Okamoto, et al.American Journal of Human Genetics|September 25, 2003
Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tractChristina L Liquori, Yoshio Ikeda, Marcy Weatherspoon, et al.Neurogenetics|December 7, 2007
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian familiesTsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, et al.Plos Genetics|August 15, 2009
RNA gain-of-function in spinocerebellar ataxia type 8Randy S Daughters, Daniel L Tuttle, Wangcai Gao, et al.Cureus|December 27, 2024
Exercise Habits, Including Exercising With Partners, and the Prevalence of Self-Reported Constipation in Young Japanese People: A Cross-Sectional StudyJunichi Watanabe, Shinya Furukawa, Yasunori Yamamoto, et al.Pageof 27