Sakuta R - Search Results

1

A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob disease.

Isozumi K, Fukuuchi Y, Tanaka K, Nogawa S, Ishihara T, Sakuta R. Isozumi K, et al. Among authors: sakuta r. Intern Med. 1994 Sep;33(9):543-6. doi: 10.2169/internalmedicine.33.543. Intern Med. 1994. PMID: 8000105 Free article.

2

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

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

4

[Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene].

Hara K, Yamamoto M, Anegawa T, Sakuta R, Nakamura M. Hara K, et al. Among authors: sakuta r. Rinsho Shinkeigaku. 1994 Apr;34(4):361-5. Rinsho Shinkeigaku. 1994. PMID: 8026131 Japanese.

5

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y, et al. Kadowaki T, et al. Among authors: sakuta r. N Engl J Med. 1994 Apr 7;330(14):962-8. doi: 10.1056/NEJM199404073301403. N Engl J Med. 1994. PMID: 8121460 Free article.

6

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

7

Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO).

Hattori Y, Goto Y, Sakuta R, Nonaka I, Mizuno Y, Horai S. Hattori Y, et al. Among authors: sakuta r. J Neurol Sci. 1994 Aug;125(1):50-5. doi: 10.1016/0022-510x(94)90241-0. J Neurol Sci. 1994. PMID: 7525879

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

9

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

10

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

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