Lin SP - Search Results

1

Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients.

Su PH, Yu JS, Wu YZ, Tsai YS, Lo FS, Lin JL, Chao MC, Hsu CC, Ke YY, Chiu PC, Chen JC, Huang YH, Lin SP, Chou YY, Ting WH, Wang SY, Chiu CF, Huang YC, Hsiao HP, Lin CH, Wang CH, Bau DT, Lin CY. Su PH, et al. Among authors: lin cy, lin ch, lin jl, lin sp. In Vivo. 2024 Jan-Feb;38(1):341-350. doi: 10.21873/invivo.13444. In Vivo. 2024. Retraction in: In Vivo. 2024 Jul-Aug;38(4):2097. doi: 10.21873/invivo.13670. PMID: 38148081 Free PMC article. Retracted.

2

Omphalocele and gastroschisis in Taiwan.

Hsu CC, Lin SP, Chen CH, Chi CS, Lee HC, Hung HY, Kao HA, Hsu CH. Hsu CC, et al. Among authors: lin sp. Eur J Pediatr. 2002 Oct;161(10):552-5. doi: 10.1007/s00431-002-1031-8. Epub 2002 Aug 15. Eur J Pediatr. 2002. PMID: 12297903

3

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: lin jl, lin sp. 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.

4

Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Yen JL, Lee YJ, Huang CY, Hung HY, Hsu CH, Kao HA, Chang JH, Chiu NC, Ho CS, Chao MC, Niu DM, Tsai LP, Kuo PL. Lin HY, et al. Among authors: lin sp. Pediatr Int. 2007 Jun;49(3):375-9. doi: 10.1111/j.1442-200X.2007.02368.x. Pediatr Int. 2007. PMID: 17532839

5

Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Chuang CK, Chen MR, Yen JL, Lee YJ, Huang CY, Tsai LP, Niu DM, Chao MC, Kuo PL. Lin HY, et al. Among authors: lin sp. Acta Paediatr. 2007 Jun;96(6):902-5. doi: 10.1111/j.1651-2227.2007.00284.x. Acta Paediatr. 2007. PMID: 17537021

6

Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients.

Lin WD, Lin SP, Wang CH, Hwu WL, Chuang CK, Lin SJ, Tsai Y, Chen CP, Tsai FJ. Lin WD, et al. Among authors: lin sj, lin sp. Clin Chim Acta. 2008 Aug;394(1-2):89-93. doi: 10.1016/j.cca.2008.04.014. Epub 2008 Apr 27. Clin Chim Acta. 2008. PMID: 18486607

7

Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndrome.

Lin HY, Lin SP, Tsai LP, Chao MC, Chen MR, Chuang CK, Huang CY, Tsai FJ, Chou IC, Chiu PC, Huang CH, Yen JL, Lin JL, Kuo PL. Lin HY, et al. Among authors: lin jl, lin sp. J Chin Med Assoc. 2008 Jun;71(6):305-9. doi: 10.1016/S1726-4901(08)70127-8. J Chin Med Assoc. 2008. PMID: 18567561 Free article.

8

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. Among authors: lin jl, lin sp. 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.

9

Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004.

Lin HY, Lin SP, Chuang CK, Niu DM, Chen MR, Tsai FJ, Chao MC, Chiu PC, Lin SJ, Tsai LP, Hwu WL, Lin JL. Lin HY, et al. Among authors: lin sj, lin jl, lin sp. Am J Med Genet A. 2009 May;149A(5):960-4. doi: 10.1002/ajmg.a.32781. Am J Med Genet A. 2009. PMID: 19396827

10

FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.

Lin WD, Chou IC, Lee NC, Wang CH, Hwu WL, Lin SP, Chao MC, Tsai Y, Tsai FJ. Lin WD, et al. Among authors: lin sp. Clin Chem Lab Med. 2010 Apr;48(4):485-8. doi: 10.1515/CCLM.2010.100. Clin Chem Lab Med. 2010. PMID: 20184535

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