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R Sakuta

Showing results (31-40 of 43) with videos related to

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Pediatric Neurology|September 1, 1992
Leigh encephalopathy: histologic and biochemical analyses of muscle biopsiesT Nagai, Y Goto, T Matsuoka, et al.
Biochemical and Biophysical Research Communications|December 30, 1993
Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory functionJ Hayashi, S Ohta, D Takai, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
No to Hattatsu = Brain and Development|January 1, 1988
[Transient improvement of the West syndrome in two cases following rotavirus colitis]Y Fujita, K Hiyoshi, N Wakasugi, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Growth hormone therapy and scoliosis in patients with Prader-Willi syndromeT Nagai, K Obata, T Ogata, et al.
Biochimica Et Biophysica Acta|December 12, 1995
Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patientsY Aoki, Y Suzuki, O Sakamoto, 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.
The New England Journal of Medicine|April 7, 1994
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNAT Kadowaki, H Kadowaki, Y Mori, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Pediatric Neurology|September 1, 1992
Leigh encephalopathy: histologic and biochemical analyses of muscle biopsiesT Nagai, Y Goto, T Matsuoka, et al.
Biochemical and Biophysical Research Communications|December 30, 1993
Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory functionJ Hayashi, S Ohta, D Takai, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
No to Hattatsu = Brain and Development|January 1, 1988
[Transient improvement of the West syndrome in two cases following rotavirus colitis]Y Fujita, K Hiyoshi, N Wakasugi, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Growth hormone therapy and scoliosis in patients with Prader-Willi syndromeT Nagai, K Obata, T Ogata, et al.
Biochimica Et Biophysica Acta|December 12, 1995
Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patientsY Aoki, Y Suzuki, O Sakamoto, 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.
The New England Journal of Medicine|April 7, 1994
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNAT Kadowaki, H Kadowaki, Y Mori, et al.
Pageof 5