Kuroda Y - Search Results

1

DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia.

Matsuda J, Ito M, Naito E, Yokota I, Kuroda Y. Matsuda J, et al. Among authors: kuroda y. J Inherit Metab Dis. 1995;18(5):534-46. doi: 10.1007/BF02435998. J Inherit Metab Dis. 1995. PMID: 8598634

2

Decrease of pyruvate dehydrogenase phosphatase activity in patients with congenital lactic acidemia.

Ito M, Kobashi H, Naito E, Saijo T, Takeda E, Huq AH, Kuroda Y. Ito M, et al. Among authors: kuroda y. Clin Chim Acta. 1992 Jul 31;209(1-2):1-7. doi: 10.1016/0009-8981(92)90327-m. Clin Chim Acta. 1992. PMID: 1327585

3

Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein.

Ito M, Huq AH, Naito E, Saijo T, Takeda E, Kuroda Y. Ito M, et al. Among authors: kuroda y. J Inherit Metab Dis. 1992;15(6):848-56. doi: 10.1007/BF01800220. J Inherit Metab Dis. 1992. PMID: 1338114

4

Clinical and biochemical findings in parents of children with vitamin D-dependent rickets Type II.

Yokota I, Takeda E, Ito M, Kobashi H, Saijo T, Kuroda Y. Yokota I, et al. Among authors: kuroda y. J Inherit Metab Dis. 1991;14(2):231-40. doi: 10.1007/BF01800596. J Inherit Metab Dis. 1991. PMID: 1653381

5

Demonstration of an unstable variant of pyruvate dehydrogenase protein (E1) in cultured fibroblasts from a patient with congenital lactic acidemia.

Huq AH, Ito M, Naito E, Saijo T, Takeda E, Kuroda Y. Huq AH, et al. Among authors: kuroda y. Pediatr Res. 1991 Jul;30(1):11-4. doi: 10.1203/00006450-199107000-00003. Pediatr Res. 1991. PMID: 1909778

6

Screening for disorders of pyruvate metabolism by measuring the ratio of the rates of lactate production and pyruvate decarboxylation in cultured skin fibroblasts.

Kuroda Y, Kawakami I, Kobashi H, Naito E, Ito M, Saijo T, Yokota I, Takeda E. Kuroda Y, et al. Clin Chim Acta. 1991 May 31;199(1):17-22. doi: 10.1016/0009-8981(91)90004-v. Clin Chim Acta. 1991. PMID: 1934498

7

A semiquantitative filter paper method for screening for lactic acidemia.

Kuroda Y, Watanabe T, Ito M, Naito E, Yokota I, Saijo T, Takeda E. Kuroda Y, et al. Tokushima J Exp Med. 1990 Jun;37(1-2):35-8. Tokushima J Exp Med. 1990. PMID: 2260086

8

Detection of pyruvate metabolism disorders by culture of skin fibroblasts with dichloroacetate.

Naito E, Kuroda Y, Takeda E, Yokota I, Kobashi H, Miyao M. Naito E, et al. Among authors: kuroda y. Pediatr Res. 1988 Jun;23(6):561-4. doi: 10.1203/00006450-198806000-00005. Pediatr Res. 1988. PMID: 2839811

9

Congenital lactic acidosis.

Kuroda Y, Naito E, Takeda E, Yokota I, Miyao M. Kuroda Y, et al. Enzyme. 1987;38(1-4):108-14. doi: 10.1159/000469196. Enzyme. 1987. PMID: 3440441

10

Molecular analysis of abnormal pyruvate dehydrogenase in a patient with thiamine-responsive congenital lactic acidemia.

Naito E, Ito M, Takeda E, Yokota I, Yoshijima S, Kuroda Y. Naito E, et al. Among authors: kuroda y. Pediatr Res. 1994 Sep;36(3):340-6. doi: 10.1203/00006450-199409000-00013. Pediatr Res. 1994. PMID: 7808831

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