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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 Disease
Masashi Ogasawara, Megumu Ogawa, Ikuya Nonaka, et al.
American Journal of Human Genetics
|
November 4, 2022
RILPL1-related OPDM is absent in a Japanese cohort
Nobuyuki 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 dystrophy
Nobuyuki 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 myopathy
May 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 myopathy
May 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 model
May 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 boy
Masashi Ogasawara, Shinji Saitoh, Yukako Nishimori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 26, 2022
Muscle biochemical and pathological diagnosis in Pompe disease
Yoshihiko Saito, Kimitoshi Nakamura, Tokiko Fukuda, et al.
Neurology
|
July 3, 2015
Plasma IP-10 level distinguishes inflammatory myopathy
Akinori 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 mutations
Mariko Okubo, Narihiro Minami, Kanako Goto, et al.
Page
of 17
Search research articles
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Showing results (31-40 of 170) with videos related to
Sort By:
Page
of 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 Disease
Masashi Ogasawara, Megumu Ogawa, Ikuya Nonaka, et al.
American Journal of Human Genetics
|
November 4, 2022
RILPL1-related OPDM is absent in a Japanese cohort
Nobuyuki 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 dystrophy
Nobuyuki 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 myopathy
May 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 myopathy
May 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 model
May 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 boy
Masashi Ogasawara, Shinji Saitoh, Yukako Nishimori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 26, 2022
Muscle biochemical and pathological diagnosis in Pompe disease
Yoshihiko Saito, Kimitoshi Nakamura, Tokiko Fukuda, et al.
Neurology
|
July 3, 2015
Plasma IP-10 level distinguishes inflammatory myopathy
Akinori 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 mutations
Mariko Okubo, Narihiro Minami, Kanako Goto, et al.
Page
of 17