Kuroda Y - Search Results

1

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

2

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

3

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

4

Diagnosis of partial deficiency of the pyruvate dehydrogenase complex in biopsied muscle.

Toshima K, Kuroda Y, Naito E, Yokota I, Ito M, Watanabe T, Takeda E, Miyao M, Nonaka I. Toshima K, et al. Among authors: kuroda y. Neurology. 1985 Nov;35(11):1670-2. doi: 10.1212/wnl.35.11.1670. Neurology. 1985. PMID: 3932899

5

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

6

Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency.

Kinoshita H, Sakuragawa N, Tada H, Naito E, Kuroda Y, Nonaka I. Kinoshita H, et al. Among authors: kuroda y. J Child Neurol. 1997 Feb;12(2):141-4. doi: 10.1177/088307389701200212. J Child Neurol. 1997. PMID: 9075024 No abstract available.

7

Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency.

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Osaka H, Kimura S, Kuroda Y. Naito E, et al. Among authors: kuroda y. J Inherit Metab Dis. 1997 Aug;20(4):539-48. doi: 10.1023/a:1005305614374. J Inherit Metab Dis. 1997. PMID: 9266390

8

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

9

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

10

[Defects of pyruvate metabolism in cultured lymphoblastoid cells of 20 patients with Leigh syndrome].

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Osaka H, Kimura S, Kuroda Y. Naito E, et al. Among authors: kuroda y. No To Hattatsu. 1996 Nov;28(6):495-500. No To Hattatsu. 1996. PMID: 8940876 Japanese.

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