Oura T - Search Results

1

Mass screening of galactosemia: improved Beutler Test using automated quantitative fluorescence assay.

Fujimoto A, Okano Y, Miyagi T, Isshiki G, Oura T. Fujimoto A, et al. Among authors: oura t. Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:69. Southeast Asian J Trop Med Public Health. 1999. PMID: 11400789 No abstract available.

2

Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader.

Fujimoto A, Okano Y, Miyagi T, Isshiki G, Oura T. Fujimoto A, et al. Among authors: oura t. Clin Chem. 2000 Jun;46(6 Pt 1):806-10. Clin Chem. 2000. PMID: 10839768

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

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

5

[DNA diagnosis for inherited metabolic disorders].

Okano Y, Oura T. Okano Y, et al. Among authors: oura t. Nihon Rinsho. 1992 Jul;50(7):1536-41. Nihon Rinsho. 1992. PMID: 1357200 Japanese.

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

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

8

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.

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

199 results

Search Page

Filters