Sakuta R - 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. 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: sakuta r. J Child Neurol. 1993 Apr;8(2):129-33. doi: 10.1177/088307389300800204. J Child Neurol. 1993. PMID: 8505474

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

4

Vascular involvement in mitochondrial myopathy.

Sakuta R, Nonaka I. Sakuta R, et al. Ann Neurol. 1989 Jun;25(6):594-601. doi: 10.1002/ana.410250611. Ann Neurol. 1989. PMID: 2500889

5

Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S. Tokunaga M, et al. Among authors: sakuta r. Ann Neurol. 1993 Mar;33(3):275-80. doi: 10.1002/ana.410330308. Ann Neurol. 1993. PMID: 7684581

6

Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNA.

Kamakura K, Abe H, Tadano Y, Nakamura R, Kobayashi H, Kawaguchi S, Nagata N, Matsuoka T, Sakuta R, Nonaka I. Kamakura K, et al. Among authors: sakuta r. J Neurol. 1995 Mar;242(4):253-5. doi: 10.1007/BF00919602. J Neurol. 1995. PMID: 7798128 No abstract available.

7

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: sakuta r. Ann Neurol. 1994 Mar;35(3):370-3. doi: 10.1002/ana.410350322. Ann Neurol. 1994. PMID: 8122892

8

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. J Neurol Sci. 1993 Apr;115(2):158-60. doi: 10.1016/0022-510x(93)90219-o. J Neurol Sci. 1993. PMID: 8482977

9

An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism.

Sakuta R, Goto Y, Nonaka I, Horai S. Sakuta R, et al. Am J Hum Genet. 1993 Oct;53(4):964-5. Am J Hum Genet. 1993. PMID: 8213827 Free PMC article. No abstract available.

10

The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings.

Ozawa M, Goto Y, Sakuta R, Tanno Y, Tsuji S, Nonaka I. Ozawa M, et al. Among authors: sakuta r. Neuromuscul Disord. 1995 Nov;5(6):483-8. doi: 10.1016/0960-8966(95)00009-c. Neuromuscul Disord. 1995. PMID: 8580730

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