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No to Hattatsu = Brain and Development|November 19, 2014
[A case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode/Leigh overlap syndrome]Jun Matsui, Tomoyuki Takano, Fukiko Ryujin, et al.
Journal of Human Genetics|February 26, 2016
Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutationsMariko Okubo, Narihiro Minami, Kanako Goto, et al.
JMA Journal|April 10, 2026
Regional Barriers to Advancing Genetic Medicine in Japan: Insights from a Shizuoka Prefecture SurveyKou Sueoka, Yuki Mizuguchi, Yasue Horiuchi, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 10, 2015
[A case of neurologic muscle weakness, ataxia, and retinitis pigmentosa (NARP) syndrome with a novel mitochondrial mutation m.8729 G>A]Toko Miyawaki, Shusuke Koto, Hiroyuki Ishihara, et al.
Journal of Human Genetics|September 26, 2017
Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutationsMariko Okubo, Narihiro Minami, Kanako Goto, et al.
International Journal of Oncology|July 10, 2013
Anti-apoptotic role of the sonic hedgehog signaling pathway in the proliferation of ameloblastomaShiori Kanda, Takeshi Mitsuyasu, Yu Nakao, et al.
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