Lo FS - Search Results

1

Polymorphism in the transmembrane region of the MICA gene and type 1 diabetes.

Lee YJ, Huang FY, Wang CH, Lo FS, Tsan KW, Hsu CH, Huang CY, Chang SC, Chang JG. Lee YJ, et al. Among authors: lo fs. J Pediatr Endocrinol Metab. 2000 May;13(5):489-96. doi: 10.1515/jpem.2000.13.5.489. J Pediatr Endocrinol Metab. 2000. PMID: 10803866

2

Solitary maxillary central incisor and congenital nasal pyriform aperture stenosis.

Lo FS, Lee YJ, Lin SP, Shen EY, Huang JK, Lee KS. Lo FS, et al. Eur J Pediatr. 1998 Jan;157(1):39-44. doi: 10.1007/s004310050763. Eur J Pediatr. 1998. PMID: 9461361 Review.

3

DQA1*Arg52,DQB1*nonAsp57, and DRB1*04 genotypes in Chinese children with insulin-dependent diabetes mellitus.

Huang FY, Lee YJ, Lo FS, Wang CH, Lin SP, Hsu CH, Kao HA, Tsan KW, Chang JG. Huang FY, et al. Among authors: lo fs. Exp Clin Immunogenet. 1998;15(1):33-45. doi: 10.1159/000019051. Exp Clin Immunogenet. 1998. PMID: 9619398

4

A freely available statistical program for testing associations.

Lee YJ, Chen MR, Chang WC, Lo FS, Huang FY. Lee YJ, et al. Among authors: lo fs. MD Comput. 1998 Sep-Oct;15(5):327-30. MD Comput. 1998. PMID: 9753980 No abstract available.

5

HLA DQA1 genotyping of Chinese in Taiwan by PCR-RFLP.

Lo FS, Chang JG, Lee YJ, Linacre A, Lee JC. Lo FS, et al. Kaohsiung J Med Sci. 1998 Aug;14(8):458-63. Kaohsiung J Med Sci. 1998. PMID: 9780594

6

Congenital nasal pyriform aperture stenosis: a diagnostic clue to solitary maxillary central incisor prior to eruption in three infants.

Lo FS, Lee KS, Chen LS, Hung HY, Hsu CH, Lin SP, Lee YJ. Lo FS, et al. J Otolaryngol. 1999 Feb;28(1):51-3. J Otolaryngol. 1999. PMID: 10077785 No abstract available.

7

Association of CTLA4 gene A-G polymorphism with type 1 diabetes in Chinese children.

Lee YJ, Huang FY, Lo FS, Wang WC, Hsu CH, Kao HA, Yang TY, Chang JG. Lee YJ, et al. Among authors: lo fs. Clin Endocrinol (Oxf). 2000 Feb;52(2):153-7. doi: 10.1046/j.1365-2265.2000.00929.x. Clin Endocrinol (Oxf). 2000. PMID: 10671941

8

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

9

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.

10

Thyroid function in children with newly diagnosed type 1 diabetes mellitus.

Lin CH, Lee YJ, Huang CY, Kao HA, Shih BF, Wang AM, Lo FS. Lin CH, et al. Among authors: lo fs. Acta Paediatr Taiwan. 2003 May-Jun;44(3):145-9. Acta Paediatr Taiwan. 2003. PMID: 14521019

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

165 results

Search Page

Filters