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Brain & Development
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June 17, 1998
Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis
M Ikezawa, N Minami, M Takahashi, et al.
Neuropediatrics
|
February 1, 1981
Alexander disease: clinical, electrodiagnostic and radiographic studies
H Nagao, K Kida, H Matsuda, et al.
Brain & Development
|
September 1, 1994
Progressive brainstem and white matter lesions in Kearns-Sayre syndrome: a case report
E Nakagawa, S Hirano, H Yamanouchi, et al.
Journal of Neurology
|
August 1, 1986
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case
M Mukoyama, H Kazui, N Sunohara, et al.
Brain & Development
|
March 1, 1996
Merosin-negative non-Fukuyama-type congenital muscular dystrophy: a case report
Y Yamashita, E Ohtaka, T Matsuishi, et al.
Immunology
|
January 1, 1996
Analysis of lymphoproliferative cytokines produced by thymic myoid cells
N Iwakami, A Kikuchi, T Kunishita, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
November 7, 1998
[The significance of Ulex europaeus agglutinin I lectin binding fibers in various muscular diseases]
K Yatabe, M Hiraguri, M Sueishi, et al.
Neurology
|
September 1, 1991
The frequency of patients with dystrophin abnormalities in a limb-girdle patient population
E Arikawa, E P Hoffman, M Kaido, et al.
Acta Neuropathologica
|
January 1, 1989
Progression in nemaline myopathy
I Nonaka, S Ishiura, K Arahata, et al.
Neurology
|
March 1, 1995
The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin
Y K Hayashi, Y Mizuno, M Yoshida, et al.
Page
of 51
Search research articles
Search
Showing results (301-310 of 503) with videos related to
Sort By:
Page
of 51
Brain & Development
|
June 17, 1998
Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis
M Ikezawa, N Minami, M Takahashi, et al.
Neuropediatrics
|
February 1, 1981
Alexander disease: clinical, electrodiagnostic and radiographic studies
H Nagao, K Kida, H Matsuda, et al.
Brain & Development
|
September 1, 1994
Progressive brainstem and white matter lesions in Kearns-Sayre syndrome: a case report
E Nakagawa, S Hirano, H Yamanouchi, et al.
Journal of Neurology
|
August 1, 1986
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case
M Mukoyama, H Kazui, N Sunohara, et al.
Brain & Development
|
March 1, 1996
Merosin-negative non-Fukuyama-type congenital muscular dystrophy: a case report
Y Yamashita, E Ohtaka, T Matsuishi, et al.
Immunology
|
January 1, 1996
Analysis of lymphoproliferative cytokines produced by thymic myoid cells
N Iwakami, A Kikuchi, T Kunishita, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
November 7, 1998
[The significance of Ulex europaeus agglutinin I lectin binding fibers in various muscular diseases]
K Yatabe, M Hiraguri, M Sueishi, et al.
Neurology
|
September 1, 1991
The frequency of patients with dystrophin abnormalities in a limb-girdle patient population
E Arikawa, E P Hoffman, M Kaido, et al.
Acta Neuropathologica
|
January 1, 1989
Progression in nemaline myopathy
I Nonaka, S Ishiura, K Arahata, et al.
Neurology
|
March 1, 1995
The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin
Y K Hayashi, Y Mizuno, M Yoshida, et al.
Page
of 51