Nonaka I - Search Results

1

A novel mtDNA C11777A mutation in Leigh syndrome.

Komaki H, Akanuma J, Iwata H, Takahashi T, Mashima Y, Nonaka I, Goto Y. Komaki H, et al. Among authors: nonaka i. Mitochondrion. 2003 Mar;2(4):293-304. doi: 10.1016/S1567-7249(03)00003-5. Mitochondrion. 2003. PMID: 16120329

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: nonaka i. 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: nonaka i. Pediatr Neurol. 1992 Sep-Oct;8(5):328-32. doi: 10.1016/0887-8994(92)90084-c. Pediatr Neurol. 1992. PMID: 1329789

4

Mitochondrial DNA mutation and Leigh's syndrome.

Sakuta R, Goto Y, Horai S, Ogino T, Yoshinaga H, Ohtahara S, Nonaka I. Sakuta R, et al. Among authors: nonaka i. Ann Neurol. 1992 Oct;32(4):597-8. doi: 10.1002/ana.410320428. Ann Neurol. 1992. PMID: 1456751 No abstract available.

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: nonaka i. 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. Among authors: nonaka i. 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. Among authors: nonaka i. Neurology. 1992 Mar;42(3 Pt 1):545-50. doi: 10.1212/wnl.42.3.545. Neurology. 1992. PMID: 1549215

8

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: nonaka i. Am J Med Genet. 1991 Mar 15;38(4):583-7. doi: 10.1002/ajmg.1320380417. Am J Med Genet. 1991. PMID: 1648309

9

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

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

10

Muscle histopathology in myoclonus epilepsy with ragged-red fibers (MERRF).

Matsuoka T, Goto Y, Yoneda M, Nonaka I. Matsuoka T, et al. Among authors: nonaka i. J Neurol Sci. 1991 Dec;106(2):193-8. doi: 10.1016/0022-510x(91)90257-8. J Neurol Sci. 1991. PMID: 1666407

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