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Ikuya Nonaka

Showing results (71-80 of 169) with videos related to

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Acta Neuropathologica|February 25, 2010
Congenital myotonic dystrophy can show congenital fiber type disproportion pathologyKayo Tominaga, Yukiko K Hayashi, Kanako Goto, et al.
Muscle & Nerve|August 9, 2016
Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2AMadoka Mori-Yoshimura, Kazuhiko Segawa, Narihiro Minami, et al.
Muscle & Nerve|November 14, 2006
Unfolded protein response and aggresome formation in hereditary reducing-body myopathyTeerin Liewluck, Yukiko K Hayashi, Maki Ohsawa, et al.
Acta Neurologica Belgica|August 7, 2002
Leber's hereditary optic neuropathy with intracranial arteriovenous malformation: a case reportJunko Fujitake, Haruo Mizuta, Hayato Fujii, et al.
Rinsho Shinkeigaku = Clinical Neurology|December 1, 2004
[A patient with distal muscular dystrophy without mutations in dysferlin gene but with abnormal dysferlin localization in muscle fibers]Isao Hozumi, Toshiaki Takahashi, Masashi Aoki, et al.
Brain & Development|February 27, 2009
Delayed gyration with pontocerebellar hypoplasia type 1Tohru Okanishi, Yuka Mori, Kenji Shirai, et al.
No to Hattatsu = Brain and Development|March 29, 2003
[Merosin-positive congenital muscular dystrophy with early orthopaedic problems in relation to Ullrich's disease]Sangmi Chang, Tatsuya Ishikawa, Ikuya Nonaka, et al.
Journal of Biochemistry|May 2, 2002
The first molecular evidence that autophagy relates rimmed vacuole formation in chloroquine myopathyTakashi Suzuki, Masahiro Nakagawa, Ayumu Yoshikawa, et al.
Acta Neuropathologica|August 4, 2010
High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulationKeiko Ishigaki, Satomi Mitsuhashi, Ryohei Kuwatsuru, et al.
Brain & Development|October 24, 2006
A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2IYi-Ching Lin, Terumi Murakami, Yukiko K Hayashi, et al.
Pageof 17

Showing results (71-80 of 169) with videos related to

Sort By:
Pageof 17
Acta Neuropathologica|February 25, 2010
Congenital myotonic dystrophy can show congenital fiber type disproportion pathologyKayo Tominaga, Yukiko K Hayashi, Kanako Goto, et al.
Muscle & Nerve|August 9, 2016
Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2AMadoka Mori-Yoshimura, Kazuhiko Segawa, Narihiro Minami, et al.
Muscle & Nerve|November 14, 2006
Unfolded protein response and aggresome formation in hereditary reducing-body myopathyTeerin Liewluck, Yukiko K Hayashi, Maki Ohsawa, et al.
Acta Neurologica Belgica|August 7, 2002
Leber's hereditary optic neuropathy with intracranial arteriovenous malformation: a case reportJunko Fujitake, Haruo Mizuta, Hayato Fujii, et al.
Rinsho Shinkeigaku = Clinical Neurology|December 1, 2004
[A patient with distal muscular dystrophy without mutations in dysferlin gene but with abnormal dysferlin localization in muscle fibers]Isao Hozumi, Toshiaki Takahashi, Masashi Aoki, et al.
Brain & Development|February 27, 2009
Delayed gyration with pontocerebellar hypoplasia type 1Tohru Okanishi, Yuka Mori, Kenji Shirai, et al.
No to Hattatsu = Brain and Development|March 29, 2003
[Merosin-positive congenital muscular dystrophy with early orthopaedic problems in relation to Ullrich's disease]Sangmi Chang, Tatsuya Ishikawa, Ikuya Nonaka, et al.
Journal of Biochemistry|May 2, 2002
The first molecular evidence that autophagy relates rimmed vacuole formation in chloroquine myopathyTakashi Suzuki, Masahiro Nakagawa, Ayumu Yoshikawa, et al.
Acta Neuropathologica|August 4, 2010
High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulationKeiko Ishigaki, Satomi Mitsuhashi, Ryohei Kuwatsuru, et al.
Brain & Development|October 24, 2006
A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2IYi-Ching Lin, Terumi Murakami, Yukiko K Hayashi, et al.
Pageof 17