Oura T - Search Results

1

Experimental research on a new treatment for maternal phenylketonuria(PKU).

Imamura T, Shintaku H, Nakajima T, Sawada Y, Isshiki G, Oura T. Imamura T, et al. Among authors: oura t. Adv Exp Med Biol. 1993;338:277-80. doi: 10.1007/978-1-4615-2960-6_57. Adv Exp Med Biol. 1993. PMID: 8304125 No abstract available.

2

Experimental research on a fetal treatment for tetrahydrobiopterin deficiency.

Shintaku H, Nakajima T, Imamura T, Sawada Y, Isshiki G, Oura T. Shintaku H, et al. Among authors: oura t. Adv Exp Med Biol. 1993;338:273-6. doi: 10.1007/978-1-4615-2960-6_56. Adv Exp Med Biol. 1993. PMID: 8304124 No abstract available.

3

Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotype.

Okano Y, Hase Y, Lee DH, Takada G, Shigematsu Y, Oura T, Isshiki G. Okano Y, et al. Among authors: oura t. J Inherit Metab Dis. 1994;17(1):156-9. doi: 10.1007/BF00735425. J Inherit Metab Dis. 1994. PMID: 8051931 No abstract available.

4

Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjects.

Shintaku H, Hsiao KJ, Liu TT, Imamura T, Hase Y, Chen RG, Isshiki G, Oura T. Shintaku H, et al. Among authors: oura t. J Inherit Metab Dis. 1994;17(1):163-6. doi: 10.1007/BF00735427. J Inherit Metab Dis. 1994. PMID: 8051934 No abstract available.

5

Molecular characterization of phenylketonuria in Japanese patients.

Okano Y, Asada M, Kang Y, Nishi Y, Hase Y, Oura T, Isshiki G. Okano Y, et al. Among authors: oura t. Hum Genet. 1998 Nov;103(5):613-8. doi: 10.1007/s004390050877. Hum Genet. 1998. PMID: 9860305

6

Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblasts.

Okano Y, Hase Y, Shintaku H, Araki K, Furuyama J, Oura T, Isshiki G. Okano Y, et al. Among authors: oura t. Hum Mol Genet. 1994 Apr;3(4):659. doi: 10.1093/hmg/3.4.659. Hum Mol Genet. 1994. PMID: 7915167 No abstract available.

7

Short tandem repeat polymorphisms in Japanese families with phenylketonuria.

Kang Y, Okano Y, Hase Y, Oura T, Isshiki G. Kang Y, et al. Among authors: oura t. J Inherit Metab Dis. 1996;19(3):375-6. doi: 10.1007/BF01799274. J Inherit Metab Dis. 1996. PMID: 8803787 No abstract available.

8

Frequency and distribution of phenylketonuric mutations in Orientals.

Okano Y, Hase Y, Lee DH, Furuyama J, Shintaku H, Oura T, Isshiki G. Okano Y, et al. Among authors: oura t. Hum Mutat. 1992;1(3):216-20. doi: 10.1002/humu.1380010307. Hum Mutat. 1992. PMID: 1301927

9

Effects of phenylalanine loading on protein synthesis in the fetal heart and brain of rat: an experimental approach to maternal phenylketonuria.

Okano Y, Chow IZ, Isshiki G, Inoue A, Oura T. Okano Y, et al. Among authors: oura t. J Inherit Metab Dis. 1986;9(1):15-24. doi: 10.1007/BF01813896. J Inherit Metab Dis. 1986. PMID: 2941618

10

Early treatment of inborn errors of biopterin metabolism.

Hase Y, Okano Y, Sawada Y, Shintaku H, Yamamoto H, Oura T. Hase Y, et al. Among authors: oura t. Acta Paediatr Jpn. 1988 Aug;30(4):390-6. doi: 10.1111/j.1442-200x.1988.tb02527.x. Acta Paediatr Jpn. 1988. PMID: 3150226 No abstract available.

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