Lin SP - Search Results

1

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. Among authors: lin sp. J Otolaryngol. 1999 Feb;28(1):51-3. J Otolaryngol. 1999. PMID: 10077785 No abstract available.

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. Among authors: lin sp. Eur J Pediatr. 1998 Jan;157(1):39-44. doi: 10.1007/s004310050763. Eur J Pediatr. 1998. PMID: 9461361 Review.

3

Frequency of associated anomalies in congenital hypoplasia of depressor anguli oris muscle: a study of 50 patients.

Lin DS, Huang FY, Lin SP, Chen MR, Kao HA, Hung HY, Hsu CH. Lin DS, et al. Among authors: lin sp. Am J Med Genet. 1997 Aug 8;71(2):215-8. Am J Med Genet. 1997. PMID: 9217225

4

Robinow syndrome: report of one case.

Wang LY, Hsu CH, Shih SL, Lin SP. Wang LY, et al. Among authors: lin sp. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 May-Jun;38(3):235-8. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997. PMID: 9230545

5

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: lin sp. Exp Clin Immunogenet. 1998;15(1):33-45. doi: 10.1159/000019051. Exp Clin Immunogenet. 1998. PMID: 9619398

6

Polymorphism of transmembrane region of MICA gene and Kawasaki disease.

Huang Y, Lee YJ, Chen MR, Hsu CH, Lin SP, Sung TC, Chang SC, Chang JG. Huang Y, et al. Among authors: lin sp. Exp Clin Immunogenet. 2000;17(3):130-7. doi: 10.1159/000019132. Exp Clin Immunogenet. 2000. PMID: 10899738

7

Congenital varicella syndrome as an unusual cause of congenital malformation: report of one case.

Huang CS, Lin SP, Chiu NC, Hung HY. Huang CS, et al. Among authors: lin sp. Acta Paediatr Taiwan. 2001 Jul-Aug;42(4):239-42. Acta Paediatr Taiwan. 2001. PMID: 11550414

8

The VATER association: analysis of forty six cases without karyotyping.

Huang LW, Chen MR, Lin SP, Huang FY, Ho MY, Kao HA, Hsu CH, Hung HY, Tsai TC. Huang LW, et al. Among authors: lin sp. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995 Jan-Feb;36(1):30-4. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995. PMID: 7778443

9

Computerized Dysmorphology Database Mackay (CDDM): preliminary report.

Hsu CH, Lin SP, Huang FY. Hsu CH, et al. Among authors: lin sp. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1994 Jan-Feb;35(1):19-26. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1994. PMID: 8178639

10

Newborns with ambiguous genitalia, impalpable gonads, and hyperpigmentation.

Chang HY, Lee YJ, Lin SP, Lee HH. Chang HY, et al. Among authors: lin sp. Acta Paediatr Taiwan. 2001 Jan-Feb;42(1):1-4. Acta Paediatr Taiwan. 2001. PMID: 11270178 No abstract available.

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