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Neuromuscular Disorders : NMD
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June 19, 2001
A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA
T Nagashima, H Kato, S Maguchi, et al.
No to Hattatsu = Brain and Development
|
September 19, 1997
[A case of congenital hypomyelination neuropathy with type I Chiari malformation and mental retardation]
Y Saito, K Sugai, M Sasaki, et al.
Immunology
|
May 1, 1995
Immunological and biochemical characterization of biglycan-like haemopoietic factor
A Kikuchi, N Iwakami, K Takahashi, et al.
The Journal of Biological Chemistry
|
January 16, 1999
alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration
S Kameya, Y Miyagoe, I Nonaka, et al.
Brain & Development
|
June 1, 1997
Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2
J Tanaka, T Nagai, H Arai, et al.
Brain & Development
|
January 1, 1987
Muscle involvement in pyruvate dehydrogenase complex (PDHC) deficiency
S J Chung, S Asoh, T Yamanaka, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegia
M Tanaka, M Yoneda, K Ohno, et al.
Brain & Development
|
January 1, 1984
Fatal lipid storage disorder
T Matsuishi, E Ono, K Terasawa, et al.
Journal of Neurology
|
July 15, 2000
Motor neuron loss in a patient with spinocerebellar ataxia type 6: chance co-occurrence or causally related?
S Ohara, J Tsuyuzaki, R Hayashi, et al.
Internal Medicine (Tokyo, Japan)
|
March 25, 2000
Necrotizing myopathy in a patient with chronic hepatitis C virus infection: a case report and a review of the literature
J Satoh, Y Eguchi, T Narukiyo, et al.
Page
of 51
Search research articles
Search
Showing results (371-380 of 503) with videos related to
Sort By:
Page
of 51
Neuromuscular Disorders : NMD
|
June 19, 2001
A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA
T Nagashima, H Kato, S Maguchi, et al.
No to Hattatsu = Brain and Development
|
September 19, 1997
[A case of congenital hypomyelination neuropathy with type I Chiari malformation and mental retardation]
Y Saito, K Sugai, M Sasaki, et al.
Immunology
|
May 1, 1995
Immunological and biochemical characterization of biglycan-like haemopoietic factor
A Kikuchi, N Iwakami, K Takahashi, et al.
The Journal of Biological Chemistry
|
January 16, 1999
alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration
S Kameya, Y Miyagoe, I Nonaka, et al.
Brain & Development
|
June 1, 1997
Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2
J Tanaka, T Nagai, H Arai, et al.
Brain & Development
|
January 1, 1987
Muscle involvement in pyruvate dehydrogenase complex (PDHC) deficiency
S J Chung, S Asoh, T Yamanaka, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegia
M Tanaka, M Yoneda, K Ohno, et al.
Brain & Development
|
January 1, 1984
Fatal lipid storage disorder
T Matsuishi, E Ono, K Terasawa, et al.
Journal of Neurology
|
July 15, 2000
Motor neuron loss in a patient with spinocerebellar ataxia type 6: chance co-occurrence or causally related?
S Ohara, J Tsuyuzaki, R Hayashi, et al.
Internal Medicine (Tokyo, Japan)
|
March 25, 2000
Necrotizing myopathy in a patient with chronic hepatitis C virus infection: a case report and a review of the literature
J Satoh, Y Eguchi, T Narukiyo, et al.
Page
of 51