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Neuromuscular Disorders : NMD
|
May 8, 2012
Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study
Yukie Inamori, Itsuro Higuchi, Teruhiko Inoue, et al.
Muscle & Nerve
|
November 1, 2005
Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency
Keiko Higashi, Itsuro Higuchi, Takahito Niiyama, et al.
Acta Neuropathologica
|
March 23, 2011
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
Yusuke Sakiyama, Yuji Okamoto, Itsuro Higuchi, et al.
Acta Neuropathologica
|
May 9, 2003
Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency
Takahito Niiyama, Itsuro Higuchi, Teruto Hashiguchi, et al.
Internal Medicine (Tokyo, Japan)
|
July 18, 2014
Partial deficiency of emerin caused by a splice site mutation in EMD
Junhui Yuan, Masahiro Ando, Itsuro Higuchi, et al.
Neurogenetics
|
June 17, 2006
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene
Yuji Okamoto, Hiroshi Takashima, Itsuro Higuchi, et al.
Journal of the Neurological Sciences
|
July 4, 2006
MRI studies of spinal visceral larva migrans syndrome
Fujio Umehara, Hideki Ookatsu, Daisuke Hayashi, et al.
Aging Cell
|
July 9, 2019
(Pro)renin receptor accelerates development of sarcopenia via activation of Wnt/YAP signaling axis
Naohiro Yoshida, Jin Endo, Kenichiro Kinouchi, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Effect of isolated AMP deaminase deficiency on skeletal muscle function
Jidong Cheng, Hiroko Morisaki, Naomi Sugimoto, et al.
International Journal of Molecular Medicine
|
September 30, 2009
Role of Kenae/CCDC125 in cell motility through the deregulation of RhoGTPase
Natsumi Araya, Hitoshi Arimura, Ko-ichi Kawahara, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
Neuromuscular Disorders : NMD
|
May 8, 2012
Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study
Yukie Inamori, Itsuro Higuchi, Teruhiko Inoue, et al.
Muscle & Nerve
|
November 1, 2005
Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency
Keiko Higashi, Itsuro Higuchi, Takahito Niiyama, et al.
Acta Neuropathologica
|
March 23, 2011
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
Yusuke Sakiyama, Yuji Okamoto, Itsuro Higuchi, et al.
Acta Neuropathologica
|
May 9, 2003
Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency
Takahito Niiyama, Itsuro Higuchi, Teruto Hashiguchi, et al.
Internal Medicine (Tokyo, Japan)
|
July 18, 2014
Partial deficiency of emerin caused by a splice site mutation in EMD
Junhui Yuan, Masahiro Ando, Itsuro Higuchi, et al.
Neurogenetics
|
June 17, 2006
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene
Yuji Okamoto, Hiroshi Takashima, Itsuro Higuchi, et al.
Journal of the Neurological Sciences
|
July 4, 2006
MRI studies of spinal visceral larva migrans syndrome
Fujio Umehara, Hideki Ookatsu, Daisuke Hayashi, et al.
Aging Cell
|
July 9, 2019
(Pro)renin receptor accelerates development of sarcopenia via activation of Wnt/YAP signaling axis
Naohiro Yoshida, Jin Endo, Kenichiro Kinouchi, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Effect of isolated AMP deaminase deficiency on skeletal muscle function
Jidong Cheng, Hiroko Morisaki, Naomi Sugimoto, et al.
International Journal of Molecular Medicine
|
September 30, 2009
Role of Kenae/CCDC125 in cell motility through the deregulation of RhoGTPase
Natsumi Araya, Hitoshi Arimura, Ko-ichi Kawahara, et al.
Page
of 7