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Journal of the Neurological Sciences
|
January 1, 1990
Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy
Y Koga, I Nonaka, M Nakao, et al.
Biochemical and Biophysical Research Communications
|
September 23, 1997
Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy
E Araki, K Nakamura, K Nakao, et al.
The Journal of Pediatrics
|
August 1, 1983
Impaired muscle fiber type differentiation in a child with nemaline myopathy
T Morimoto, H Nagao, N Sano, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy
Y K Hayashi, Z Tezak, T Momoi, et al.
Neurology
|
September 6, 2007
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
M Okada, G Kawahara, S Noguchi, et al.
Muscle & Nerve
|
September 1, 1995
Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy
Y K Hayashi, R Koga, T Tsukahara, et al.
Brain & Development
|
May 1, 1995
A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
H Kinoshita, Y Goto, M Ishikawa, et al.
Neurology
|
August 13, 2003
A neonatal form of glycogen storage disease type IV
M Nambu, K Kawabe, T Fukuda, et al.
Biology of Reproduction
|
August 22, 2003
Complement C4b-binding protein as a novel murine epididymal secretory protein
Mayumi I Nonaka, Yoshitaka Hishikawa, Nobuo Moriyama, et al.
Acta Neuropathologica
|
January 1, 1988
Muscle pathology in cytochrome c oxidase deficiency
I Nonaka, Y Koga, K Shikura, et al.
Page
of 51
Search research articles
Search
Showing results (401-410 of 503) with videos related to
Sort By:
Page
of 51
Journal of the Neurological Sciences
|
January 1, 1990
Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy
Y Koga, I Nonaka, M Nakao, et al.
Biochemical and Biophysical Research Communications
|
September 23, 1997
Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy
E Araki, K Nakamura, K Nakao, et al.
The Journal of Pediatrics
|
August 1, 1983
Impaired muscle fiber type differentiation in a child with nemaline myopathy
T Morimoto, H Nagao, N Sano, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy
Y K Hayashi, Z Tezak, T Momoi, et al.
Neurology
|
September 6, 2007
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
M Okada, G Kawahara, S Noguchi, et al.
Muscle & Nerve
|
September 1, 1995
Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy
Y K Hayashi, R Koga, T Tsukahara, et al.
Brain & Development
|
May 1, 1995
A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
H Kinoshita, Y Goto, M Ishikawa, et al.
Neurology
|
August 13, 2003
A neonatal form of glycogen storage disease type IV
M Nambu, K Kawabe, T Fukuda, et al.
Biology of Reproduction
|
August 22, 2003
Complement C4b-binding protein as a novel murine epididymal secretory protein
Mayumi I Nonaka, Yoshitaka Hishikawa, Nobuo Moriyama, et al.
Acta Neuropathologica
|
January 1, 1988
Muscle pathology in cytochrome c oxidase deficiency
I Nonaka, Y Koga, K Shikura, et al.
Page
of 51