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Satoru Noguchi

Showing results (91-100 of 170) with videos related to

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Plos One|December 20, 2012
Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathiesKazunari Momma, Satoru Noguchi, May Christine V Malicdan, et al.
Neuromuscular Disorders : NMD|June 18, 2016
Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308]Kohei Hamanaka, Kanako Goto, Mami Arai, et al.
Neurology|December 5, 2020
Pathologic Features of Anti-Mi-2 DermatomyositisJantima Tanboon, Michio Inoue, Shinya Hirakawa, et al.
Genome Medicine|March 27, 2026
Pathogenic CGG expansions in oculopharyngodistal myopathy exhibit distinct characteristics of each causative gene on the flanking sequences as well as methylation statusNobuyuki Eura, Satoru Noguchi, Megumu Ogawa, et al.
Inorganic Chemistry|July 18, 2006
Magnetoresistance effects evidencing the pi-d interaction in metallic organic conductors, (EDT-DSDTFVO)2*MX4 (M = Fe, Ga; X = Cl, Br)Hideki Fujiwara, Toshiki Hayashi, Toyonari Sugimoto, et al.
Muscle & Nerve|July 22, 2008
Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytesGenri Kawahara, Megumu Ogawa, Mari Okada, et al.
Brain Pathology (Zurich, Switzerland)|March 7, 2023
Muscle pathology of antisynthetase syndrome according to antibody subtypesJantima Tanboon, Michio Inoue, Shinya Hirakawa, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1BYoung-Eun Park, Yukiko K Hayashi, Kanako Goto, et al.
Muscle & Nerve|April 14, 2026
Spatiotemporal Patterns of Fat Replacement in SELENON-Related Myopathy: A Whole-Body Imaging StudyRui Shimazaki, Satoru Noguchi, Wakako Yoshioka, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Pageof 17

Showing results (91-100 of 170) with videos related to

Sort By:
Pageof 17
Plos One|December 20, 2012
Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathiesKazunari Momma, Satoru Noguchi, May Christine V Malicdan, et al.
Neuromuscular Disorders : NMD|June 18, 2016
Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308]Kohei Hamanaka, Kanako Goto, Mami Arai, et al.
Neurology|December 5, 2020
Pathologic Features of Anti-Mi-2 DermatomyositisJantima Tanboon, Michio Inoue, Shinya Hirakawa, et al.
Genome Medicine|March 27, 2026
Pathogenic CGG expansions in oculopharyngodistal myopathy exhibit distinct characteristics of each causative gene on the flanking sequences as well as methylation statusNobuyuki Eura, Satoru Noguchi, Megumu Ogawa, et al.
Inorganic Chemistry|July 18, 2006
Magnetoresistance effects evidencing the pi-d interaction in metallic organic conductors, (EDT-DSDTFVO)2*MX4 (M = Fe, Ga; X = Cl, Br)Hideki Fujiwara, Toshiki Hayashi, Toyonari Sugimoto, et al.
Muscle & Nerve|July 22, 2008
Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytesGenri Kawahara, Megumu Ogawa, Mari Okada, et al.
Brain Pathology (Zurich, Switzerland)|March 7, 2023
Muscle pathology of antisynthetase syndrome according to antibody subtypesJantima Tanboon, Michio Inoue, Shinya Hirakawa, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1BYoung-Eun Park, Yukiko K Hayashi, Kanako Goto, et al.
Muscle & Nerve|April 14, 2026
Spatiotemporal Patterns of Fat Replacement in SELENON-Related Myopathy: A Whole-Body Imaging StudyRui Shimazaki, Satoru Noguchi, Wakako Yoshioka, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Pageof 17