Wu SJ - Search Results

1

Tetrahydrobiopterin-deficient hyperphenylalaninemia in the Chinese.

Liu TT, Chiang SH, Wu SJ, Hsiao KJ. Liu TT, et al. Among authors: wu sj. Clin Chim Acta. 2001 Nov;313(1-2):157-69. doi: 10.1016/s0009-8981(01)00669-6. Clin Chim Acta. 2001. PMID: 11694255

2

Mutation analysis of the 6-pyruvoyl-tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency.

Liu TT, Hsiao KJ, Lu SF, Wu SJ, Wu KF, Chiang SH, Liu XQ, Chen RG, Yu WM. Liu TT, et al. Among authors: wu sj, wu kf. Hum Mutat. 1998;11(1):76-83. doi: 10.1002/(SICI)1098-1004(1998)11:1<76::AID-HUMU12>3.0.CO;2-W. Hum Mutat. 1998. PMID: 9450907

3

Identification of a novel point mutation (S65T) in alpha-galactosidase A gene in Chinese patients with Fabry disease. Mutations in brief no. 169. Online.

Chen CH, Shyu PW, Wu SJ, Sheu SS, Desnick RJ, Hsiao KJ. Chen CH, et al. Among authors: wu sj. Hum Mutat. 1998;11(4):328-30. doi: 10.1002/(SICI)1098-1004(1998)11:4<328::AID-HUMU11>3.0.CO;2-N. Hum Mutat. 1998. PMID: 9554750

4

Neonatal screening for glucose-6-phosphate dehydrogenase deficiency in Taiwan.

Chiang SH, Wu SJ, Wu KF, Hsiao KJ. Chiang SH, et al. Among authors: wu sj, wu kf. Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:72-4. Southeast Asian J Trop Med Public Health. 1999. PMID: 11400791

5

Determination of erythrocyte glutathione peroxidase activity and its reference range in Chinese adults.

Yeh SL, Wu SJ, Shieh MJ, Hsiao KJ. Yeh SL, et al. Among authors: wu sj. J Formos Med Assoc. 1990 Jul;89(7):519-25. J Formos Med Assoc. 1990. PMID: 1979592

6

Erythrocyte hydroxymethylbilane synthase activity in a Chinese family with acute intermittent porphyria.

Lee FY, Hsiao KJ, Tsai YT, Lee SD, Wu SJ, Jeng HS. Lee FY, et al. Among authors: wu sj. Ann Clin Biochem. 1988 Nov;25 ( Pt 6):706-7. doi: 10.1177/000456328802500618. Ann Clin Biochem. 1988. PMID: 3254113 No abstract available.

7

Determination of erythrocyte porphobilinogen deaminase activity using porphobilinogen as substrate.

Hsiao KJ, Lee FY, Wu SJ, Chang WJ. Hsiao KJ, et al. Among authors: wu sj. Clin Chim Acta. 1987 Sep 30;168(2):257-8. doi: 10.1016/0009-8981(87)90296-8. Clin Chim Acta. 1987. PMID: 3677422 No abstract available.

8

Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese children.

Hsiao KJ, Chen CH, Liu TT, Wu SJ, Plettner C, Clemens P. Hsiao KJ, et al. Among authors: wu sj. Taiwan Yi Xue Hui Za Zhi. 1989 Jan;88(1):18-22. Taiwan Yi Xue Hui Za Zhi. 1989. PMID: 2787833

9

Gas chromatographic analysis of abnormal urinary organic acids in phenylketonuria.

Hsiao KJ, Hung SH, Wu SJ, Yeh SF. Hsiao KJ, et al. Among authors: wu sj. Taiwan Yi Xue Hui Za Zhi. 1985 Nov;84(11):1240-50. Taiwan Yi Xue Hui Za Zhi. 1985. PMID: 3868699 No abstract available.

10

Determination of erythrocyte hydroxymethylbilane synthase activity and its application for study of acute intermittent porphyria.

Lee FY, Hsiao KJ, Tsai YT, Lee SD, Wu SJ, Jeng HS. Lee FY, et al. Among authors: wu sj. Taiwan Yi Xue Hui Za Zhi. 1988 Nov;87(11):1029-35. Taiwan Yi Xue Hui Za Zhi. 1988. PMID: 3235962 No abstract available.

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