Sakuta R - Search Results

1

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.

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

Pyruvate Improved Insulin Secretion Status in a Mitochondrial Diabetes Mellitus Patient.

Inoue T, Murakami N, Ayabe T, Oto Y, Nishino I, Goto Y, Koga Y, Sakuta R. Inoue T, et al. Among authors: sakuta r. J Clin Endocrinol Metab. 2016 May;101(5):1924-6. doi: 10.1210/jc.2015-4293. Epub 2016 Feb 17. J Clin Endocrinol Metab. 2016. PMID: 26885883

4

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. Kim DS, et al. Among authors: sakuta r. Neurology. 2004 Mar 23;62(6):1009-11. doi: 10.1212/01.wnl.0000115386.28769.65. Neurology. 2004. PMID: 15037715

5

Hypertrophy of the cerebral white matter in hemimegalencephaly.

Kato M, Mizuguchi M, Sakuta R, Takashima S. Kato M, et al. Among authors: sakuta r. Pediatr Neurol. 1996 May;14(4):335-8. doi: 10.1016/0887-8994(96)00057-4. Pediatr Neurol. 1996. PMID: 8962592

6

Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia.

Nagai T, Tuchiya Y, Maruyama A, Sakuta R, Nonaka I. Nagai T, et al. Among authors: sakuta r. Pediatr Neurol. 1993 May-Jun;9(3):239-42. doi: 10.1016/0887-8994(93)90094-s. Pediatr Neurol. 1993. PMID: 8352860

7

Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficiencies.

Nagai T, Tuchiya Y, Taguchi Y, Sakuta R, Ichiki T, Nonaka I. Nagai T, et al. Among authors: sakuta r. Pediatr Neurol. 1993 Mar-Apr;9(2):151-4. doi: 10.1016/0887-8994(93)90054-g. Pediatr Neurol. 1993. PMID: 8388688

8

Dysembryoplastic neuroepithelial tumors in childhood: long-term outcome and prognostic features.

Nolan MA, Sakuta R, Chuang N, Otsubo H, Rutka JT, Snead OC 3rd, Hawkins CE, Weiss SK. Nolan MA, et al. Among authors: sakuta r. Neurology. 2004 Jun 22;62(12):2270-6. doi: 10.1212/01.wnl.0000130495.69512.6f. Neurology. 2004. PMID: 15210893

9

Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus.

Kadowaki H, Tobe K, Mori Y, Sakura H, Sakuta R, Nonaka I, Hagura R, Yazaki Y, Akanuma Y, Kadowaki T. Kadowaki H, et al. Among authors: sakuta r. Lancet. 1993 Apr 3;341(8849):893-4. doi: 10.1016/0140-6736(93)93101-6. Lancet. 1993. PMID: 8096591 No abstract available.

10

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

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