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Ikuya Nonaka

Showing results (111-120 of 169) with videos related to

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Human Molecular Genetics|March 15, 2006
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathiesMariko Taniguchi, Hiroki Kurahashi, Satoru Noguchi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 20, 2011
Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrestHisashi Kawashima, Chiako Ishii, Gaku Yamanaka, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.
The American Journal of Pathology|September 2, 2014
Dietary phosphorus overload aggravates the phenotype of the dystrophin-deficient mdx mouseEiji Wada, Mizuko Yoshida, Yoriko Kojima, et al.
Journal of the Neurological Sciences|October 2, 2010
A case with central and peripheral hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) plus cataractIkuko Sato, Akira Onuma, Nobue Goto, et al.
Neuromuscular Disorders : NMD|January 14, 2012
A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvementAyako Hattori, Hirofumi Komaki, Masao Kawatani, et al.
Mitochondrion|May 23, 2009
Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disordersMasakazu Mimaki, Hideyuki Hatakeyama, Takashi Ichiyama, et al.
Neurology. Genetics|April 12, 2016
Milder forms of muscular dystrophy associated with POMGNT2 mutationsYukari Endo, Mingrui Dong, Satoru Noguchi, et al.
Neuromuscular Disorders : NMD|May 8, 2022
Myoglobinopathy affecting facial and oropharyngeal musclesYuka Hama, Madoka Mori-Yoshimura, Kazutaka Aizawa, et al.
Pageof 17

Showing results (111-120 of 169) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|March 15, 2006
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathiesMariko Taniguchi, Hiroki Kurahashi, Satoru Noguchi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 20, 2011
Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrestHisashi Kawashima, Chiako Ishii, Gaku Yamanaka, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.
The American Journal of Pathology|September 2, 2014
Dietary phosphorus overload aggravates the phenotype of the dystrophin-deficient mdx mouseEiji Wada, Mizuko Yoshida, Yoriko Kojima, et al.
Journal of the Neurological Sciences|October 2, 2010
A case with central and peripheral hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) plus cataractIkuko Sato, Akira Onuma, Nobue Goto, et al.
Neuromuscular Disorders : NMD|January 14, 2012
A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvementAyako Hattori, Hirofumi Komaki, Masao Kawatani, et al.
Mitochondrion|May 23, 2009
Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disordersMasakazu Mimaki, Hideyuki Hatakeyama, Takashi Ichiyama, et al.
Neurology. Genetics|April 12, 2016
Milder forms of muscular dystrophy associated with POMGNT2 mutationsYukari Endo, Mingrui Dong, Satoru Noguchi, et al.
Neuromuscular Disorders : NMD|May 8, 2022
Myoglobinopathy affecting facial and oropharyngeal musclesYuka Hama, Madoka Mori-Yoshimura, Kazutaka Aizawa, et al.
Pageof 17