Goto Y - Search Results

1

Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis.

Ikezawa M, Minami N, Takahashi M, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: goto y. Brain Dev. 1998 Apr;20(3):165-8. doi: 10.1016/s0387-7604(98)00012-6. Brain Dev. 1998. PMID: 9628192

2

Segmental cytochrome c-oxidase deficiency in CPEO: teased muscle fiber analysis.

Matsuoka T, Goto Y, Hasegawa H, Nonaka I. Matsuoka T, et al. Among authors: goto y. Muscle Nerve. 1992 Feb;15(2):209-13. doi: 10.1002/mus.880150213. Muscle Nerve. 1992. PMID: 1312676

3

Leigh encephalopathy: histologic and biochemical analyses of muscle biopsies.

Nagai T, Goto Y, Matsuoka T, Sakuta R, Naito E, Kuroda Y, Nonaka I. Nagai T, et al. Among authors: goto y. Pediatr Neurol. 1992 Sep-Oct;8(5):328-32. doi: 10.1016/0887-8994(92)90084-c. Pediatr Neurol. 1992. PMID: 1329789

4

A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: a case report.

Shigihara-Yasuda K, Tonoki H, Goto Y, Arahata K, Ishikawa N, Kajii N, Fujieda K. Shigihara-Yasuda K, et al. Among authors: goto y. Eur J Pediatr. 1992 Jan;151(1):66-8. doi: 10.1007/BF02073897. Eur J Pediatr. 1992. PMID: 1370218

5

An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administration.

Wu CM, Matsuoka T, Takemitsu M, Goto Y, Nonaka I. Wu CM, et al. Among authors: goto y. Muscle Nerve. 1992 Nov;15(11):1258-64. doi: 10.1002/mus.880151107. Muscle Nerve. 1992. PMID: 1488063

6

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.

Goto Y, Tojo M, Tohyama J, Horai S, Nonaka I. Goto Y, et al. Ann Neurol. 1992 Jun;31(6):672-5. doi: 10.1002/ana.410310617. Ann Neurol. 1992. PMID: 1514779

7

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I. Goto Y, et al. Neurology. 1992 Mar;42(3 Pt 1):545-50. doi: 10.1212/wnl.42.3.545. Neurology. 1992. PMID: 1549215

8

[Vascular pathology in chronic progressive external ophthalmoplegia with ragged-red fibers].

Hasegawa H, Matsuoka T, Goto Y, Nonaka I. Hasegawa H, et al. Among authors: goto y. Rinsho Shinkeigaku. 1992 Feb;32(2):155-60. Rinsho Shinkeigaku. 1992. PMID: 1611773 Japanese.

9

Renal and skin involvement in a patient with complete Kearns-Sayre syndrome.

Mori K, Narahara K, Ninomiya S, Goto Y, Nonaka I. Mori K, et al. Among authors: goto y. Am J Med Genet. 1991 Mar 15;38(4):583-7. doi: 10.1002/ajmg.1320380417. Am J Med Genet. 1991. PMID: 1648309

10

Mitochondrial encephalomyopathies and cytochrome c oxidase deficiency: muscle culture study.

Nonaka I, Koga Y, Kikuchi A, Goto Y. Nonaka I, et al. Among authors: goto y. Acta Neuropathol. 1991;82(4):286-94. doi: 10.1007/BF00308814. Acta Neuropathol. 1991. PMID: 1662001

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