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Showing results (451-460 of 503) with videos related to

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American Journal of Medical Genetics|December 18, 1998
Four novel mutations of the connexin 32 gene in four Japanese families with Charcot-Marie-Tooth disease type 1T Ikegami, C Lin, M Kato, et al.
Journal of the Neurological Sciences|December 16, 1998
Lysosomal glycogen storage disease with normal acid maltase with early fatal outcomeY Morisawa, M Fujieda, N Murakami, et al.
Lancet (London, England)|April 3, 1993
Mitochondrial gene mutation and insulin-deficient type of diabetes mellitusH Kadowaki, K Tobe, Y Mori, et al.
Journal of Neurology|March 1, 1995
Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNAK Kamakura, H Abe, Y Tadano, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
In vitro activation of the pyruvate dehydrogenase complex in human muscle by a broad specificity protein phosphataseK Toshima, Y Kuroda, E Takeda, et al.
Pediatric Research|February 1, 1989
Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathyT Ichiki, M Tanaka, M Kobayashi, et al.
Human Molecular Genetics|March 21, 1998
Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of beta-dystroglycan in the outer plexiform layer of the retinaS Kameya, E Araki, M Katsuki, et al.
Biochemical and Biophysical Research Communications|August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyT Ozawa, M Yoneda, M Tanaka, et al.
Journal of the Neurological Sciences|August 28, 1999
A case of McLeod syndrome with unusually severe myopathyT Kawakami, Y Takiyama, K Sakoe, et al.
Journal of Gravitational Physiology : a Journal of the International Society for Gravitational Physiology|April 17, 2003
Dependence of normal development of skeletal muscle in neonatal rats on load bearingY Ohira, T Tanaka, T Yoshinaga, et al.
Pageof 51

Showing results (451-460 of 503) with videos related to

Sort By:
Pageof 51
American Journal of Medical Genetics|December 18, 1998
Four novel mutations of the connexin 32 gene in four Japanese families with Charcot-Marie-Tooth disease type 1T Ikegami, C Lin, M Kato, et al.
Journal of the Neurological Sciences|December 16, 1998
Lysosomal glycogen storage disease with normal acid maltase with early fatal outcomeY Morisawa, M Fujieda, N Murakami, et al.
Lancet (London, England)|April 3, 1993
Mitochondrial gene mutation and insulin-deficient type of diabetes mellitusH Kadowaki, K Tobe, Y Mori, et al.
Journal of Neurology|March 1, 1995
Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNAK Kamakura, H Abe, Y Tadano, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
In vitro activation of the pyruvate dehydrogenase complex in human muscle by a broad specificity protein phosphataseK Toshima, Y Kuroda, E Takeda, et al.
Pediatric Research|February 1, 1989
Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathyT Ichiki, M Tanaka, M Kobayashi, et al.
Human Molecular Genetics|March 21, 1998
Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of beta-dystroglycan in the outer plexiform layer of the retinaS Kameya, E Araki, M Katsuki, et al.
Biochemical and Biophysical Research Communications|August 15, 1988
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyT Ozawa, M Yoneda, M Tanaka, et al.
Journal of the Neurological Sciences|August 28, 1999
A case of McLeod syndrome with unusually severe myopathyT Kawakami, Y Takiyama, K Sakoe, et al.
Journal of Gravitational Physiology : a Journal of the International Society for Gravitational Physiology|April 17, 2003
Dependence of normal development of skeletal muscle in neonatal rats on load bearingY Ohira, T Tanaka, T Yoshinaga, et al.
Pageof 51