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I Nonaka

Showing results (351-360 of 503) with videos related to

Pageof 51
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Neuropediatrics|September 10, 1999
Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletionS Fujimoto, T Ishikawa, M Saito, et al.
Muscle & Nerve|July 9, 1999
Transforming growth factor-beta2 is elevated in skeletal muscle disordersN Murakami, I S McLennan, I Nonaka, et al.
Neurology|September 10, 2003
Preservation of branchimotor neurons of the nucleus ambiguus in multiple system atrophyK Ikeda, Y Iwasaki, A Kuwajima, et al.
Neurology|September 12, 2001
Infantile autophagic vacuolar myopathy is distinct from Danon diseaseA Yamamoto, Y Morisawa, A Verloes, et al.
Journal of the Neurological Sciences|April 1, 1995
Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathyT Nara, M Akashi, I Nonaka, et al.
Neurology|September 26, 2002
Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weaknessH Ishikawa, K Sugie, K Murayama, et al.
Pathology, Research and Practice|July 4, 2001
Muscle plasma membrane changes in dystrophin gene exon 52 knockout mouseS Shibuya, Y Wakayama, M Murahashi, et al.
Cellular Immunology|September 1, 1985
Effects of thymic myoid cell culture supernatant on cells from lymphatic tissuesI Kamo, A Tada-Kikuchi, S Furukawa, et al.
Muscle & Nerve. Supplement|January 1, 1995
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.
Journal of Cell Science|January 14, 1998
Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophiesB L Hodges, Y K Hayashi, I Nonaka, et al.
Pageof 51

Showing results (351-360 of 503) with videos related to

Sort By:
Pageof 51
Neuropediatrics|September 10, 1999
Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletionS Fujimoto, T Ishikawa, M Saito, et al.
Muscle & Nerve|July 9, 1999
Transforming growth factor-beta2 is elevated in skeletal muscle disordersN Murakami, I S McLennan, I Nonaka, et al.
Neurology|September 10, 2003
Preservation of branchimotor neurons of the nucleus ambiguus in multiple system atrophyK Ikeda, Y Iwasaki, A Kuwajima, et al.
Neurology|September 12, 2001
Infantile autophagic vacuolar myopathy is distinct from Danon diseaseA Yamamoto, Y Morisawa, A Verloes, et al.
Journal of the Neurological Sciences|April 1, 1995
Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathyT Nara, M Akashi, I Nonaka, et al.
Neurology|September 26, 2002
Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weaknessH Ishikawa, K Sugie, K Murayama, et al.
Pathology, Research and Practice|July 4, 2001
Muscle plasma membrane changes in dystrophin gene exon 52 knockout mouseS Shibuya, Y Wakayama, M Murahashi, et al.
Cellular Immunology|September 1, 1985
Effects of thymic myoid cell culture supernatant on cells from lymphatic tissuesI Kamo, A Tada-Kikuchi, S Furukawa, et al.
Muscle & Nerve. Supplement|January 1, 1995
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.
Journal of Cell Science|January 14, 1998
Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophiesB L Hodges, Y K Hayashi, I Nonaka, et al.
Pageof 51