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Acta Neuropathologica
|
January 1, 1995
Immunohistochemical study of calpain and its endogenous inhibitor in the skeletal muscle of muscular dystrophy
T Kumamoto, H Ueyama, S Watanabe, et al.
Brain & Development
|
January 1, 1989
Clinical improvement of adrenoleukodystrophy following intravenous gammaglobulin therapy
T Miike, K Taku, T Tamura, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine
|
November 1, 1990
[123I-IMP single photon emission computed tomography (SPECT) study in childhood epilepsy]
M Hara, O Shimomura, A Kojima, et al.
No to Hattatsu = Brain and Development
|
May 29, 2000
[Nation-wide survey on hemimegalencephaly in Japan]
M Sasaki, T Hashimoto, M Shimada, et al.
No to Hattatsu = Brain and Development
|
July 1, 1989
[A case of mitochondrial encephalomyopathy with cardiomyopathy due to decreased complex I and IV activities]
M Kajiyama, I Kawamura, A Fujita, et al.
American Journal of Medical Genetics
|
November 1, 1988
Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients
T Matsumoto, T Kondoh, M Yoshimoto, et al.
Annals of Neurology
|
June 1, 1995
Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat
T Ikeuchi, R Koide, H Tanaka, et al.
American Journal of Medical Genetics
|
December 1, 1989
Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females
S Sugino, S Fujishita, N Kamimura, et al.
Brain & Development
|
March 7, 2006
Immobility reduces muscle fiber necrosis in dystrophin deficient muscular dystrophy
S Kimura, M Ikezawa, K Nomura, et al.
Annals of Neurology
|
December 16, 1998
Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy
S Kimura, S Sugino, Y Ohtani, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 95) with videos related to
Sort By:
Page
of 10
Acta Neuropathologica
|
January 1, 1995
Immunohistochemical study of calpain and its endogenous inhibitor in the skeletal muscle of muscular dystrophy
T Kumamoto, H Ueyama, S Watanabe, et al.
Brain & Development
|
January 1, 1989
Clinical improvement of adrenoleukodystrophy following intravenous gammaglobulin therapy
T Miike, K Taku, T Tamura, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine
|
November 1, 1990
[123I-IMP single photon emission computed tomography (SPECT) study in childhood epilepsy]
M Hara, O Shimomura, A Kojima, et al.
No to Hattatsu = Brain and Development
|
May 29, 2000
[Nation-wide survey on hemimegalencephaly in Japan]
M Sasaki, T Hashimoto, M Shimada, et al.
No to Hattatsu = Brain and Development
|
July 1, 1989
[A case of mitochondrial encephalomyopathy with cardiomyopathy due to decreased complex I and IV activities]
M Kajiyama, I Kawamura, A Fujita, et al.
American Journal of Medical Genetics
|
November 1, 1988
Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients
T Matsumoto, T Kondoh, M Yoshimoto, et al.
Annals of Neurology
|
June 1, 1995
Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat
T Ikeuchi, R Koide, H Tanaka, et al.
American Journal of Medical Genetics
|
December 1, 1989
Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females
S Sugino, S Fujishita, N Kamimura, et al.
Brain & Development
|
March 7, 2006
Immobility reduces muscle fiber necrosis in dystrophin deficient muscular dystrophy
S Kimura, M Ikezawa, K Nomura, et al.
Annals of Neurology
|
December 16, 1998
Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy
S Kimura, S Sugino, Y Ohtani, et al.
Page
of 10