Nonaka I - Search Results

1

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.

Mitsuhashi S, Hatakeyama H, Karahashi M, Koumura T, Nonaka I, Hayashi YK, Noguchi S, Sher RB, Nakagawa Y, Manfredi G, Goto Y, Cox GA, Nishino I. Mitsuhashi S, et al. Among authors: nonaka i. Hum Mol Genet. 2011 Oct 1;20(19):3841-51. doi: 10.1093/hmg/ddr305. Epub 2011 Jul 12. Hum Mol Genet. 2011. PMID: 21750112 Free PMC article.

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

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

5

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

6

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

7

[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: nonaka i. Rinsho Shinkeigaku. 1992 Feb;32(2):155-60. Rinsho Shinkeigaku. 1992. PMID: 1611773 Japanese.

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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