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Ikuya Nonaka

Showing results (61-70 of 169) with videos related to

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Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|October 14, 2003
Altered expression of ARPP protein in skeletal muscles of patients with muscular dystrophy, congenital myopathy and spinal muscular atrophyChisato Nakada, Yoshiyuki Tsukamoto, Akira Oka, et al.
Journal of Human Genetics|November 24, 2017
Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathyHaruhito Harada, Takeharu Hayashi, Hirofumi Nishi, et al.
Human Genome Variation|August 8, 2018
A novel <i>LMNA</i> mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophyAkihiko Ishiyama, Aritoshi Iida, Shinichiro Hayashi, et al.
Annals of Neurology|March 11, 2011
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathyWen-Chen Liang, Hiroaki Mitsuhashi, Etsuko Keduka, et al.
Neuromuscular Disorders : NMD|May 5, 2019
Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvementLin Ge, Xiaona Fu, Wei Zhang, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Homozygous female Becker muscular dystrophyKatsunori Fujii, Narihiro Minami, Yukiko Hayashi, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 2009
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patientSherine Shalaby, Hiroaki Mitsuhashi, Chie Matsuda, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Two novel CAV3 gene mutations in Japanese familiesKazuma Sugie, Kumiko Murayama, Satoru Noguchi, et al.
The American Journal of Pathology|March 2, 2006
Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuolesRitsuko Ozawa, Yukiko K Hayashi, Megumu Ogawa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2013
Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophyTakahiro Yonekawa, Hirofumi Komaki, Mari Okada, et al.
Pageof 17

Showing results (61-70 of 169) with videos related to

Sort By:
Pageof 17
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|October 14, 2003
Altered expression of ARPP protein in skeletal muscles of patients with muscular dystrophy, congenital myopathy and spinal muscular atrophyChisato Nakada, Yoshiyuki Tsukamoto, Akira Oka, et al.
Journal of Human Genetics|November 24, 2017
Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathyHaruhito Harada, Takeharu Hayashi, Hirofumi Nishi, et al.
Human Genome Variation|August 8, 2018
A novel <i>LMNA</i> mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophyAkihiko Ishiyama, Aritoshi Iida, Shinichiro Hayashi, et al.
Annals of Neurology|March 11, 2011
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathyWen-Chen Liang, Hiroaki Mitsuhashi, Etsuko Keduka, et al.
Neuromuscular Disorders : NMD|May 5, 2019
Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvementLin Ge, Xiaona Fu, Wei Zhang, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Homozygous female Becker muscular dystrophyKatsunori Fujii, Narihiro Minami, Yukiko Hayashi, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 2009
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patientSherine Shalaby, Hiroaki Mitsuhashi, Chie Matsuda, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Two novel CAV3 gene mutations in Japanese familiesKazuma Sugie, Kumiko Murayama, Satoru Noguchi, et al.
The American Journal of Pathology|March 2, 2006
Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuolesRitsuko Ozawa, Yukiko K Hayashi, Megumu Ogawa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2013
Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophyTakahiro Yonekawa, Hirofumi Komaki, Mari Okada, et al.
Pageof 17