Nonaka I - Search Results

1

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.

2

A T-to-G mutation at nucleotide pair 8993 in mitochondrial DNA in a patient with Leigh's syndrome.

Yoshinaga H, Ogino T, Ohtahara S, Sakuta R, Nonaka I, Horai S. Yoshinaga H, et al. Among authors: nonaka i. J Child Neurol. 1993 Apr;8(2):129-33. doi: 10.1177/088307389300800204. J Child Neurol. 1993. PMID: 8505474

3

Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.

Kawakami Y, Sakuta R, Hashimoto K, Fujino O, Fujita T, Hida M, Horai S, Goto Y, Nonaka I. Kawakami Y, et al. Among authors: nonaka i. Ann Neurol. 1994 Mar;35(3):370-3. doi: 10.1002/ana.410350322. Ann Neurol. 1994. PMID: 8122892

4

Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative study.

Sakuta R, Goto Y, Horai S, Nonaka I. Sakuta R, et al. Among authors: nonaka i. J Neurol Sci. 1993 Apr;115(2):158-60. doi: 10.1016/0022-510x(93)90219-o. J Neurol Sci. 1993. PMID: 8482977

5

[Mitochondrial encephalomyopathies: 3243 mutation as a central matter].

Goto Y, Nonaka I. Goto Y, et al. Among authors: nonaka i. Rinsho Shinkeigaku. 1995 Dec;35(12):1425-6. Rinsho Shinkeigaku. 1995. PMID: 8752418 Review. Japanese.

6

Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome.

Makino M, Horai S, Goto Y, Nonaka I. Makino M, et al. Among authors: nonaka i. Neuromuscul Disord. 1998 May;8(3-4):149-51. doi: 10.1016/s0960-8966(98)00017-0. Neuromuscul Disord. 1998. PMID: 9631394

7

Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications.

Makino M, Horai S, Goto Y, Nonaka I. Makino M, et al. Among authors: nonaka i. J Hum Genet. 2000;45(2):69-75. doi: 10.1007/s100380050014. J Hum Genet. 2000. PMID: 10721666

8

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

9

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

10

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

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