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The New England Journal of Medicine
|
January 19, 1989
Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy
K Arahata, T Ishihara, K Kamakura, et al.
Journal of the Neurological Sciences
|
January 1, 1997
Muscle histopathology in diabetes mellitus associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243
Y Suzuki, Y Goto, M Taniyama, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Cerebral oxygen and glucose metabolism in glycogen storage disease with normal acid maltase: case report
Y Katsumi, H Fukuyama, M Ogawa, et al.
Neuromuscular Disorders : NMD
|
September 1, 1995
A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin
E Arikawa-Hirasawa, R Koga, T Tsukahara, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics
|
December 1, 1986
[An autopsy case of lung cancer in a young adult dwarf]
S Saijo, Y Saijo, T Hirosawa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1992
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy
A H Beggs, P E Neumann, K Arahata, et al.
Neurology
|
November 1, 1985
Diagnosis of partial deficiency of the pyruvate dehydrogenase complex in biopsied muscle
K Toshima, Y Kuroda, E Naito, et al.
Internal Medicine (Tokyo, Japan)
|
December 1, 1996
Mitochondrial encephalomyopathy with elderly onset of stroke-like episodes
H Minamoto, K Kawabata, B Okuda, et al.
Journal of the Neurological Sciences
|
October 1, 1993
Abnormal localization of laminin subunits in muscular dystrophies
Y K Hayashi, E Engvall, E Arikawa-Hirasawa, et al.
The Journal of Pediatrics
|
February 1, 1987
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
M Kobayashi, H Morishita, N Sugiyama, et al.
Page
of 51
Search research articles
Search
Showing results (421-430 of 503) with videos related to
Sort By:
Page
of 51
The New England Journal of Medicine
|
January 19, 1989
Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy
K Arahata, T Ishihara, K Kamakura, et al.
Journal of the Neurological Sciences
|
January 1, 1997
Muscle histopathology in diabetes mellitus associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243
Y Suzuki, Y Goto, M Taniyama, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Cerebral oxygen and glucose metabolism in glycogen storage disease with normal acid maltase: case report
Y Katsumi, H Fukuyama, M Ogawa, et al.
Neuromuscular Disorders : NMD
|
September 1, 1995
A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin
E Arikawa-Hirasawa, R Koga, T Tsukahara, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics
|
December 1, 1986
[An autopsy case of lung cancer in a young adult dwarf]
S Saijo, Y Saijo, T Hirosawa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1992
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy
A H Beggs, P E Neumann, K Arahata, et al.
Neurology
|
November 1, 1985
Diagnosis of partial deficiency of the pyruvate dehydrogenase complex in biopsied muscle
K Toshima, Y Kuroda, E Naito, et al.
Internal Medicine (Tokyo, Japan)
|
December 1, 1996
Mitochondrial encephalomyopathy with elderly onset of stroke-like episodes
H Minamoto, K Kawabata, B Okuda, et al.
Journal of the Neurological Sciences
|
October 1, 1993
Abnormal localization of laminin subunits in muscular dystrophies
Y K Hayashi, E Engvall, E Arikawa-Hirasawa, et al.
The Journal of Pediatrics
|
February 1, 1987
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
M Kobayashi, H Morishita, N Sugiyama, et al.
Page
of 51