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Neuropediatrics
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September 10, 1999
Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion
S Fujimoto, T Ishikawa, M Saito, et al.
Muscle & Nerve
|
July 9, 1999
Transforming growth factor-beta2 is elevated in skeletal muscle disorders
N Murakami, I S McLennan, I Nonaka, et al.
Neurology
|
September 10, 2003
Preservation of branchimotor neurons of the nucleus ambiguus in multiple system atrophy
K Ikeda, Y Iwasaki, A Kuwajima, et al.
Neurology
|
September 12, 2001
Infantile autophagic vacuolar myopathy is distinct from Danon disease
A Yamamoto, Y Morisawa, A Verloes, et al.
Journal of the Neurological Sciences
|
April 1, 1995
Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy
T Nara, M Akashi, I Nonaka, et al.
Neurology
|
September 26, 2002
Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness
H Ishikawa, K Sugie, K Murayama, et al.
Pathology, Research and Practice
|
July 4, 2001
Muscle plasma membrane changes in dystrophin gene exon 52 knockout mouse
S Shibuya, Y Wakayama, M Murahashi, et al.
Cellular Immunology
|
September 1, 1985
Effects of thymic myoid cell culture supernatant on cells from lymphatic tissues
I Kamo, A Tada-Kikuchi, S Furukawa, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses
K 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 dystrophies
B L Hodges, Y K Hayashi, I Nonaka, et al.
Page
of 51
Search research articles
Search
Showing results (351-360 of 503) with videos related to
Sort By:
Page
of 51
Neuropediatrics
|
September 10, 1999
Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion
S Fujimoto, T Ishikawa, M Saito, et al.
Muscle & Nerve
|
July 9, 1999
Transforming growth factor-beta2 is elevated in skeletal muscle disorders
N Murakami, I S McLennan, I Nonaka, et al.
Neurology
|
September 10, 2003
Preservation of branchimotor neurons of the nucleus ambiguus in multiple system atrophy
K Ikeda, Y Iwasaki, A Kuwajima, et al.
Neurology
|
September 12, 2001
Infantile autophagic vacuolar myopathy is distinct from Danon disease
A Yamamoto, Y Morisawa, A Verloes, et al.
Journal of the Neurological Sciences
|
April 1, 1995
Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy
T Nara, M Akashi, I Nonaka, et al.
Neurology
|
September 26, 2002
Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness
H Ishikawa, K Sugie, K Murayama, et al.
Pathology, Research and Practice
|
July 4, 2001
Muscle plasma membrane changes in dystrophin gene exon 52 knockout mouse
S Shibuya, Y Wakayama, M Murahashi, et al.
Cellular Immunology
|
September 1, 1985
Effects of thymic myoid cell culture supernatant on cells from lymphatic tissues
I Kamo, A Tada-Kikuchi, S Furukawa, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses
K 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 dystrophies
B L Hodges, Y K Hayashi, I Nonaka, et al.
Page
of 51