Miyabayashi S - Search Results

1

Extensive defects of mitochondrial electron-transfer chain in muscular cytochrome c oxidase deficiency.

Tanaka M, Miyabayashi S, Nishikimi M, Suzuki H, Shimomura Y, Ito K, Narisawa K, Tada K, Ozawa T. Tanaka M, et al. Among authors: miyabayashi s. Pediatr Res. 1988 Oct;24(4):447-54. doi: 10.1203/00006450-198810000-00006. Pediatr Res. 1988. PMID: 2845344

2

Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy.

Haginoya K, Miyabayashi S, Iinuma K, Okino E, Maesaka H, Tada K. Haginoya K, et al. Among authors: miyabayashi s. Pediatr Neurol. 1992 Jan-Feb;8(1):13-8. doi: 10.1016/0887-8994(92)90046-2. Pediatr Neurol. 1992. PMID: 1313674

3

Chronic pancreatitis in muscular cytochrome c oxidase deficiency.

Kato S, Miyabayashi S, Ohi R, Nakagawa H, Abe J, Yamamoto K, Watanabe S, Tada K. Kato S, et al. Among authors: miyabayashi s. J Pediatr Gastroenterol Nutr. 1990 Nov;11(4):549-52. doi: 10.1097/00005176-199011000-00018. J Pediatr Gastroenterol Nutr. 1990. PMID: 2175784

4

Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase.

Haginoya K, Miyabayashi S, Iinuma K, Tada K. Haginoya K, et al. Among authors: miyabayashi s. Acta Neuropathol. 1990;80(6):642-8. doi: 10.1007/BF00307633. Acta Neuropathol. 1990. PMID: 2177307

5

Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy.

Miyabayashi S, Haginoya K, Hanamizu H, Iinuma K, Narisawa K, Tada K. Miyabayashi S, et al. J Inherit Metab Dis. 1989;12(3):373-7. doi: 10.1007/BF01799245. J Inherit Metab Dis. 1989. PMID: 2559247 No abstract available.

6

Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.

Miyabayashi S, Ito T, Abukawa D, Narisawa K, Tada K, Tanaka M, Ozawa T, Droste M, Kadenbach B. Miyabayashi S, et al. J Inherit Metab Dis. 1987;10(3):289-92. doi: 10.1007/BF01800084. J Inherit Metab Dis. 1987. PMID: 2828763 No abstract available.

7

Cytochrome C oxidase deficiency in two siblings with Leigh encephalomyelopathy.

Miyabayashi S, Narisawa K, Iinuma K, Tada K, Sakai K, Kobayashi K, Kobayashi Y, Morinaga S. Miyabayashi S, et al. Brain Dev. 1984;6(4):362-72. doi: 10.1016/s0387-7604(84)80112-6. Brain Dev. 1984. PMID: 6093613

8

Two siblings with cytochrome c oxidase deficiency.

Miyabayashi S, Narisawa K, Tada K, Sakai K, Kobayashi K, Kobayashi Y. Miyabayashi S, et al. J Inherit Metab Dis. 1983;6(3):121-2. doi: 10.1007/BF01800742. J Inherit Metab Dis. 1983. PMID: 6321854 No abstract available.

9

Thiamine responsive pyruvate dehydrogenase deficiency.

Narisawa K, Endo H, Miyabayashi S, Tada K. Narisawa K, et al. Among authors: miyabayashi s. J Nutr Sci Vitaminol (Tokyo). 1992;Spec No:585-8. doi: 10.3177/jnsv.38.special_585. J Nutr Sci Vitaminol (Tokyo). 1992. PMID: 1297818

10

Genetic heterogeneity of propionic acidemia: analysis of 15 Japanese patients.

Ohura T, Miyabayashi S, Narisawa K, Tada K. Ohura T, et al. Among authors: miyabayashi s. Hum Genet. 1991 May;87(1):41-4. doi: 10.1007/BF01213089. Hum Genet. 1991. PMID: 2037281

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