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Satoru Noguchi

Showing results (31-40 of 170) with videos related to

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Journal of Neuropathology and Experimental Neurology|November 13, 2020
Evaluation of the Core Formation Process in Congenital Neuromuscular Disease With Uniform Type 1 Fiber and Central Core DiseaseMasashi Ogasawara, Megumu Ogawa, Ikuya Nonaka, et al.
American Journal of Human Genetics|November 4, 2022
RILPL1-related OPDM is absent in a Japanese cohortNobuyuki Eura, Aritoshi Iida, Masashi Ogasawara, et al.
Journal of Neurology|August 27, 2023
Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophyNobuyuki Eura, Satoru Noguchi, Masashi Ogasawara, et al.
Human Molecular Genetics|December 14, 2006
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathyMay Christine V Malicdan, Satoru Noguchi, Ikuya Nonaka, et al.
Human Molecular Genetics|August 21, 2007
A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathyMay Christine V Malicdan, Satoru Noguchi, Ikuya Nonaka, et al.
Nature Medicine|May 19, 2009
Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse modelMay Christine V Malicdan, Satoru Noguchi, Yukiko K Hayashi, et al.
Neuromuscular Disorders : NMD|October 29, 2022
Malignant hyperthermia and cylindrical spirals in a 4-year-old boyMasashi Ogasawara, Shinji Saitoh, Yukako Nishimori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 26, 2022
Muscle biochemical and pathological diagnosis in Pompe diseaseYoshihiko Saito, Kimitoshi Nakamura, Tokiko Fukuda, et al.
Neurology|July 3, 2015
Plasma IP-10 level distinguishes inflammatory myopathyAkinori Uruha, Satoru Noguchi, Wakiro Sato, 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.
Pageof 17

Showing results (31-40 of 170) with videos related to

Sort By:
Pageof 17
Journal of Neuropathology and Experimental Neurology|November 13, 2020
Evaluation of the Core Formation Process in Congenital Neuromuscular Disease With Uniform Type 1 Fiber and Central Core DiseaseMasashi Ogasawara, Megumu Ogawa, Ikuya Nonaka, et al.
American Journal of Human Genetics|November 4, 2022
RILPL1-related OPDM is absent in a Japanese cohortNobuyuki Eura, Aritoshi Iida, Masashi Ogasawara, et al.
Journal of Neurology|August 27, 2023
Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophyNobuyuki Eura, Satoru Noguchi, Masashi Ogasawara, et al.
Human Molecular Genetics|December 14, 2006
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathyMay Christine V Malicdan, Satoru Noguchi, Ikuya Nonaka, et al.
Human Molecular Genetics|August 21, 2007
A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathyMay Christine V Malicdan, Satoru Noguchi, Ikuya Nonaka, et al.
Nature Medicine|May 19, 2009
Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse modelMay Christine V Malicdan, Satoru Noguchi, Yukiko K Hayashi, et al.
Neuromuscular Disorders : NMD|October 29, 2022
Malignant hyperthermia and cylindrical spirals in a 4-year-old boyMasashi Ogasawara, Shinji Saitoh, Yukako Nishimori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 26, 2022
Muscle biochemical and pathological diagnosis in Pompe diseaseYoshihiko Saito, Kimitoshi Nakamura, Tokiko Fukuda, et al.
Neurology|July 3, 2015
Plasma IP-10 level distinguishes inflammatory myopathyAkinori Uruha, Satoru Noguchi, Wakiro Sato, 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.
Pageof 17