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Yasushi Oya

Showing results (71-80 of 95) with videos related to

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Journal of Neurology|December 12, 2024
Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosisSo Okubo, Hiroya Naruse, Hiroyuki Ishiura, et al.
Clinical Neurology and Neurosurgery|May 23, 2012
Clinicopathological features of centronuclear myopathy in Japanese populations harboring mutations in dynamin 2Madoka Mori-Yoshimura, Aya Okuma, Yasushi Oya, et al.
Journal of Inherited Metabolic Disease|October 11, 2011
Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up studyYoshihiko Furusawa, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of Clinical Neuromuscular Disease|May 26, 2016
Chronic Myopathy Associated With Anti-Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular DystrophyKensuke Ikeda, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of the Peripheral Nervous System : JPNS|February 29, 2020
Clinical features of inherited neuropathy with BSCL2 mutations in JapanSatoshi Ishihara, Yuji Okamoto, Hajime Tanabe, et al.
BMC Medicine|November 19, 2020
The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx miceYasunari Matsuzaka, Jun Tanihata, Yoshiko Ooshima, et al.
Neurology|July 11, 2020
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical featuresYoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, et al.
Scientific Reports|December 16, 2022
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathyWakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, et al.
Acta Neuropathologica Communications|November 26, 2020
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestationsMasashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, et al.
Muscle & Nerve|June 20, 2015
Respiratory and cardiac function in japanese patients with dysferlinopathyAtsuko Nishikawa, Madoka Mori-Yoshimura, Kazuhiko Segawa, et al.
Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:
Pageof 10
Journal of Neurology|December 12, 2024
Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosisSo Okubo, Hiroya Naruse, Hiroyuki Ishiura, et al.
Clinical Neurology and Neurosurgery|May 23, 2012
Clinicopathological features of centronuclear myopathy in Japanese populations harboring mutations in dynamin 2Madoka Mori-Yoshimura, Aya Okuma, Yasushi Oya, et al.
Journal of Inherited Metabolic Disease|October 11, 2011
Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up studyYoshihiko Furusawa, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of Clinical Neuromuscular Disease|May 26, 2016
Chronic Myopathy Associated With Anti-Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular DystrophyKensuke Ikeda, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of the Peripheral Nervous System : JPNS|February 29, 2020
Clinical features of inherited neuropathy with BSCL2 mutations in JapanSatoshi Ishihara, Yuji Okamoto, Hajime Tanabe, et al.
BMC Medicine|November 19, 2020
The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx miceYasunari Matsuzaka, Jun Tanihata, Yoshiko Ooshima, et al.
Neurology|July 11, 2020
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical featuresYoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, et al.
Scientific Reports|December 16, 2022
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathyWakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, et al.
Acta Neuropathologica Communications|November 26, 2020
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestationsMasashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, et al.
Muscle & Nerve|June 20, 2015
Respiratory and cardiac function in japanese patients with dysferlinopathyAtsuko Nishikawa, Madoka Mori-Yoshimura, Kazuhiko Segawa, et al.
Pageof 10