Wang TR - Search Results

1

Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan.

Su PH, Hwu WL, Chiang SC, Chiu PC, Lin SJ, Shu SG, Wang TR. Su PH, et al. Among authors: wang tr. J Formos Med Assoc. 1998 Mar;97(3):186-90. J Formos Med Assoc. 1998. PMID: 9549269

2

Quantification of arylsulfatase B activity and diagnosis of Maroteaux-Lamy syndrome.

Hwu WL, Wang TR. Hwu WL, et al. Among authors: wang tr. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991 Sep-Oct;32(5):280-5. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991. PMID: 1776456

3

Cardiovascular disorders in Turner's syndrome and its correlation to karyotype.

Hou JW, Hwu WL, Tsai WY, Lee JS, Wang TR, Lue HC. Hou JW, et al. Among authors: wang tr. J Formos Med Assoc. 1993 Feb;92(2):188-9. J Formos Med Assoc. 1993. PMID: 8101751

4

Diagnosis of mucopolysaccharidosis type IIIB.

Chuang SC, Hwu WL, Wu CC, Hou JW, Wang TR. Chuang SC, et al. Among authors: wang tr. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1996 Sep-Oct;37(5):320-3. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1996. PMID: 8942024

5

DNA fingerprinting in the Chinese with an oligonucleotide probe (GTG)5.

Hwu WL, Chen RL, Lin KH, Wang TR. Hwu WL, et al. Among authors: wang tr. J Formos Med Assoc. 1992 Sep;91(9):839-43. J Formos Med Assoc. 1992. PMID: 1363381

6

Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment.

Chien YH, Chiang SC, Huang A, Lin JM, Chiu YN, Chou SP, Wang TR, Hwu WL. Chien YH, et al. Among authors: wang tr. Acta Paediatr Taiwan. 2004 Nov-Dec;45(6):320-3. Acta Paediatr Taiwan. 2004. PMID: 15868846

7

A clinical observation of achondroplasia.

Hwu WL, Wang TR. Hwu WL, et al. Among authors: wang tr. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991 Jul-Aug;32(4):208-13. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991. PMID: 1776446

8

Alkaptonuria in a Chinese baby.

Wang TR, Hwu WL. Wang TR, et al. J Inherit Metab Dis. 1989;12(3):327. doi: 10.1007/BF01799226. J Inherit Metab Dis. 1989. PMID: 2515375 No abstract available.

9

Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family.

Wang TR, Lin SJ. Wang TR, et al. Am J Med Genet. 1987 Oct;28(2):471-5. doi: 10.1002/ajmg.1320280224. Am J Med Genet. 1987. PMID: 3425620

10

Prevalence of permanent primary congenital hypothyroidism in Taiwan.

Tsai WY, Lee JS, Chao MC, Chen LY, Lin SJ, Wu KH, Wang TR, Chen JS, Chuang SM. Tsai WY, et al. Among authors: wang tr. J Formos Med Assoc. 1995 May;94(5):271-3. J Formos Med Assoc. 1995. PMID: 7613262

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