Lo FS - Search Results

1

Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.

Lee HH, Chang SF, Lo FS, Chao HT, Lin CY. Lee HH, et al. Among authors: lo fs. Mol Genet Metab. 2003 Jul;79(3):214-20. doi: 10.1016/s1096-7192(03)00087-8. Mol Genet Metab. 2003. PMID: 12855227

2

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.

Lee HH, Lee YJ, Wang YM, Chao HT, Niu DM, Chao MC, Tsai FJ, Lo FS, Lin SJ. Lee HH, et al. Among authors: lo fs. Mol Genet Metab. 2008 Apr;93(4):450-7. doi: 10.1016/j.ymgme.2007.10.008. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18039588

3

Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency.

Lee HH, Chang SF, Lee YJ, Raskin S, Lin SJ, Chao MC, Lo FS, Lin CY. Lee HH, et al. Among authors: lo fs. Clin Chem. 2003 Feb;49(2):319-22. doi: 10.1373/49.2.319. Clin Chem. 2003. PMID: 12560361 No abstract available.

4

The promoter region of the CTLA4 gene is associated with type 1 diabetes mellitus.

Lee YJ, Lo FS, Shu SG, Wang CH, Huang CY, Liu HF, Wu CC, Yang TY, Chang JG. Lee YJ, et al. Among authors: lo fs. J Pediatr Endocrinol Metab. 2001 Apr;14(4):383-8. doi: 10.1515/jpem.2001.14.4.383. J Pediatr Endocrinol Metab. 2001. PMID: 11327371

5

Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children.

Tsai ST, Huang CY, Lo FS, Chang YT, Tanizawa T, Chen CK, Wang ZC, Liu HF, Chu CC, Lin M, Lin CH, Li HJ, Lee YJ. Tsai ST, et al. Among authors: lo fs. J Pediatr Endocrinol Metab. 2008 Jul;21(7):665-72. doi: 10.1515/jpem.2008.21.7.665. J Pediatr Endocrinol Metab. 2008. PMID: 18780601

6

The CBLB gene and Graves' disease in children.

Chen CC, Huang CY, Huang FY, Dang CW, Lin CL, Lo FS, Lin CH, Tsang CC, Li HJ, Liu HF, Chu CC, Lin M, Lee YJ. Chen CC, et al. Among authors: lo fs. J Pediatr Endocrinol Metab. 2005 Nov;18(11):1119-26. doi: 10.1515/jpem.2005.18.11.1119. J Pediatr Endocrinol Metab. 2005. PMID: 16459459

7

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature.

Lo FS, Lin JL, Kuo MT, Chiu PC, Shu SG, Chao MC, Lee YJ, Lin SP. Lo FS, et al. Eur J Pediatr. 2009 Aug;168(8):919-23. doi: 10.1007/s00431-008-0858-z. Epub 2008 Oct 29. Eur J Pediatr. 2009. PMID: 18958496 Review.

8

Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese.

Wu YL, Hwang DY, Hsiao HP, Ting WH, Huang CY, Tsai WY, Chen HC, Chao MC, Lo FS, Tsai JD, Yang S, Shih SL, Lin SP, Lin CL, Lee YJ. Wu YL, et al. Among authors: lo fs. PLoS One. 2014 Mar 20;9(3):e90640. doi: 10.1371/journal.pone.0090640. eCollection 2014. PLoS One. 2014. PMID: 24651309 Free PMC article.

9

Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome.

Hung CS, Lin JL, Lee YJ, Lin SP, Chao MC, Lo FS. Hung CS, et al. Among authors: lo fs. J Formos Med Assoc. 2007 Feb;106(2):169-72. doi: 10.1016/S0929-6646(09)60235-7. J Formos Med Assoc. 2007. PMID: 17339163 Free article.

10

Short form of the Chinese version Diabetes Quality of Life for Youth Scale: a psychometric testing in Taiwanese adolescents with type 1 diabetes.

Wang RH, Lo FS, Chen BH, Hsu HY, Lee YJ. Wang RH, et al. Among authors: lo fs. Diabetes Care. 2011 Sep;34(9):1943-5. doi: 10.2337/dc11-0705. Epub 2011 Jul 25. Diabetes Care. 2011. PMID: 21788630 Free PMC article.

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