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Biochemical and Biophysical Research Communications
|
August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy
I Nishino, A Seki, Y Maegaki, et al.
Acta Orthopaedica Scandinavica
|
April 1, 1994
A histochemical study of the biceps brachii muscle cross-innervated by intercostal nerves. 6 cases of brachial plexus injuries operated with nerve-crossing
H Kawai, T Murase, H Kawabata, et al.
No to Hattatsu = Brain and Development
|
January 1, 1991
[Carnitine palmitoyltransferase deficiency in a patient with severe psychomotor retardation]
H Suzuki, Y Hirayama, S Hirano, et al.
Annals of Neurology
|
April 1, 1990
Cerebral cortex and brainstem involvement in Marinesco-Sjögren syndrome
Y Katafuchi, K Kosai, E Ohtaki, et al.
Nature
|
August 5, 1993
Myogenin gene disruption results in perinatal lethality because of severe muscle defect
Y Nabeshima, K Hanaoka, M Hayasaka, et al.
Brain & Development
|
April 1, 1997
Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers (MERRF): a single-photon emission computed tomographic (SPECT) and electrophysiological study
S Tanaka, S Osari, M Ozawa, et al.
Japanese Journal of Medicine
|
July 1, 1982
Adult form acid maltase deficiency -- a case report
A Akamatsu, R Nomoto, H Nagao, et al.
Biochemical Pharmacology
|
August 11, 1998
Study on the inhibitory effect of tannins and flavonoids against the 1,1-diphenyl-2 picrylhydrazyl radical
T Yokozawa, C P Chen, E Dong, et al.
Neurology
|
March 1, 1992
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation
Y Goto, S Horai, T Matsuoka, et al.
Neuropediatrics
|
November 1, 1983
Congenital myopathy without specific features (minimal change myopathy)
I Nonaka, Y Nakamura, M Tojo, et al.
Page
of 51
Search research articles
Search
Showing results (331-340 of 503) with videos related to
Sort By:
Page
of 51
Biochemical and Biophysical Research Communications
|
August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy
I Nishino, A Seki, Y Maegaki, et al.
Acta Orthopaedica Scandinavica
|
April 1, 1994
A histochemical study of the biceps brachii muscle cross-innervated by intercostal nerves. 6 cases of brachial plexus injuries operated with nerve-crossing
H Kawai, T Murase, H Kawabata, et al.
No to Hattatsu = Brain and Development
|
January 1, 1991
[Carnitine palmitoyltransferase deficiency in a patient with severe psychomotor retardation]
H Suzuki, Y Hirayama, S Hirano, et al.
Annals of Neurology
|
April 1, 1990
Cerebral cortex and brainstem involvement in Marinesco-Sjögren syndrome
Y Katafuchi, K Kosai, E Ohtaki, et al.
Nature
|
August 5, 1993
Myogenin gene disruption results in perinatal lethality because of severe muscle defect
Y Nabeshima, K Hanaoka, M Hayasaka, et al.
Brain & Development
|
April 1, 1997
Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers (MERRF): a single-photon emission computed tomographic (SPECT) and electrophysiological study
S Tanaka, S Osari, M Ozawa, et al.
Japanese Journal of Medicine
|
July 1, 1982
Adult form acid maltase deficiency -- a case report
A Akamatsu, R Nomoto, H Nagao, et al.
Biochemical Pharmacology
|
August 11, 1998
Study on the inhibitory effect of tannins and flavonoids against the 1,1-diphenyl-2 picrylhydrazyl radical
T Yokozawa, C P Chen, E Dong, et al.
Neurology
|
March 1, 1992
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation
Y Goto, S Horai, T Matsuoka, et al.
Neuropediatrics
|
November 1, 1983
Congenital myopathy without specific features (minimal change myopathy)
I Nonaka, Y Nakamura, M Tojo, et al.
Page
of 51