Kuno T - Search Results

1

Clinical characteristics of Angelman syndrome patients with a non-IC-deleted imprinting mutation.

Saitoh S, Wada T, Kuno T, Kim KC, Ohashi H, Hashimoto K, Niikawa N. Saitoh S, et al. Among authors: kuno t. Clin Genet. 1999 Apr;55(4):277-8. doi: 10.1034/j.1399-0004.1999.550411.x. Clin Genet. 1999. PMID: 10361990 No abstract available.

2

The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients.

Nishiyori A, Yoshino M, Kato H, Matsuura T, Hoshide R, Matsuda I, Kuno T, Miyazaki S, Hirose S, Kuromaru R, Mori M. Nishiyori A, et al. Among authors: kuno t. Hum Genet. 1997 Feb;99(2):171-6. doi: 10.1007/s004390050333. Hum Genet. 1997. PMID: 9048915

3

Late-onset ornithine transcarbamylase deficiency in male patients: prognostic factors and characteristics of plasma amino acid profile.

Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M. Harada E, et al. Among authors: kuno t. Pediatr Int. 2006 Apr;48(2):105-11. doi: 10.1111/j.1442-200X.2006.02181.x. Pediatr Int. 2006. PMID: 16635166

4

Plasma beta-carotene, retinol, and alpha-tocopherol levels in relation to glycemic control of children with insulin-dependent diabetes mellitus.

Hozumi M, Murata T, Morinobu T, Manago M, Kuno T, Tokuda M, Konishi K, Mingci Z, Tamai H. Hozumi M, et al. Among authors: kuno t. J Nutr Sci Vitaminol (Tokyo). 1998 Feb;44(1):1-9. doi: 10.3177/jnsv.44.1. J Nutr Sci Vitaminol (Tokyo). 1998. PMID: 9591229

5

Rapid decrease of urinary pyridinoline excretion in growth hormone deficient children following discontinuation of growth hormone therapy.

Kuno T, Tasaki H, Miyazaki S, Horie H. Kuno T, et al. Acta Paediatr Jpn. 1997 Feb;39(1):18-20. doi: 10.1111/j.1442-200x.1997.tb03549.x. Acta Paediatr Jpn. 1997. PMID: 9124047

6

Central diabetes insipidus: an ominous sign in severe hypoxic encephalopathy.

Hojo M, Kuno T, Sakamoto K, Hamasaki Y, Miyazaki S, Kuroiwa T, Nishima S. Hojo M, et al. Among authors: kuno t. Acta Paediatr Scand. 1990 Jun-Jul;79(6-7):701-3. doi: 10.1111/j.1651-2227.1990.tb11539.x. Acta Paediatr Scand. 1990. PMID: 2386066 No abstract available.

7

Hyperammonemia caused by impaired mitochondrial ornithine transport in a patient with partial quantitative deficiency of ornithine carbamoyltransferase.

Kuno T, Miyazaki S, Inoue I, Saheki T. Kuno T, et al. Clin Biochem. 1990 Apr;23(2):143-7. doi: 10.1016/0009-9120(90)80027-g. Clin Biochem. 1990. PMID: 2372929

8

Continuous subcutaneous insulin injection for a case of mitochondrial cytopathy with diabetes mellitus requiring a large amount of insulin.

Kuno T, Tashiro K, Sato T, Tasaki H, Miyazaki S. Kuno T, et al. Pediatr Int. 1999 Feb;41(1):97-100. doi: 10.1046/j.1442-200x.1999.01002.x. Pediatr Int. 1999. PMID: 10200145 No abstract available.

9

[Late-onset type ornitine transcarbamirase deficiency (OTCD) with fulminant onset following a fatal prognosis].

Yasutake T, Nagatomo D, Mizuta T, Eguchi Y, Kumagai T, Ario K, Ozaki I, Kuno T, Fujimoto K. Yasutake T, et al. Among authors: kuno t. Nihon Shokakibyo Gakkai Zasshi. 2007 Dec;104(12):1752-7. Nihon Shokakibyo Gakkai Zasshi. 2007. PMID: 18057853 Japanese.

10

Antioxidant vitamin levels in plasma and low density lipoprotein of obese girls.

Kuno T, Hozumi M, Morinobu T, Murata T, Mingci Z, Tamai H. Kuno T, et al. Free Radic Res. 1998 Jan;28(1):81-6. doi: 10.3109/10715769809097878. Free Radic Res. 1998. PMID: 9554835

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