Lin SP - Search Results

1

Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients With Severe Illnesses.

Wu ET, Hwu WL, Chien YH, Hsu C, Chen TF, Chen NQ, Chou HC, Tsao PN, Fan PC, Tsai IJ, Lin SP, Hsieh WS, Chang TM, Chen CN, Lee CH, Chou YY, Chiu PC, Tsai WH, Hsiung HC, Lai F, Lee NC. Wu ET, et al. Among authors: lin sp. Pediatr Crit Care Med. 2019 Nov;20(11):1021-1026. doi: 10.1097/PCC.0000000000002068. Pediatr Crit Care Med. 2019. PMID: 31261230

2

Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in Prader-Willi syndrome and Duchenne muscular dystrophy.

Hung CC, Chen CP, Lin SP, Chien SC, Lee CN, Cheng WF, Hsieh WS, Liu MS, Su YN, Lin WL. Hung CC, et al. Among authors: lin wl, lin sp. Clin Chem. 2006 Dec;52(12):2203-10. doi: 10.1373/clinchem.2006.071118. Epub 2006 Oct 13. Clin Chem. 2006. PMID: 17040959

3

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

4

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.

5

Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR.

Hung CC, Lin SY, Lin SP, Niu DM, Lee NC, Cheng WF, Chen CP, Lin WL, Lee CN, Su YN. Hung CC, et al. Among authors: lin sy, lin wl, lin sp. Electrophoresis. 2009 Jan;30(2):410-6. doi: 10.1002/elps.200800225. Electrophoresis. 2009. PMID: 19137525

6

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

7

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

8

Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in Taiwan.

Cheng KH, Liu MY, Kao CH, Chen YJ, Hsiao KJ, Liu TT, Lin HY, Huang CH, Chiang CC, Ho HJ, Lin SP, Lee NC, Hwu WL, Lin JL, Hung PY, Niu DM. Cheng KH, et al. Among authors: lin jl, lin hy, lin sp. J Chin Med Assoc. 2010 Jun;73(6):314-8. doi: 10.1016/S1726-4901(10)70067-8. J Chin Med Assoc. 2010. PMID: 20603089 Free article.

9

Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome.

Lin SY, Lee CN, Hung CC, Tsai WY, Lin SP, Li NC, Hsieh WS, Tung YC, Niu DM, Hsu WM, Chen LY, Fang MY, Tu MP, Kuo PW, Lin CY, Su YN, Ho HN. Lin SY, et al. Among authors: lin cy, lin sp. Am J Med Genet A. 2010 Oct;152A(10):2521-8. doi: 10.1002/ajmg.a.33629. Am J Med Genet A. 2010. PMID: 20830799

10

Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan.

Lin HY, Chen MR, Chuang CK, Chen CP, Lin DS, Chien YH, Ke YY, Tsai FJ, Pan HP, Lin SJ, Hwu WL, Niu DM, Lee NC, Lin SP. Lin HY, et al. Among authors: lin sj, lin sp, lin ds. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S421-7. doi: 10.1007/s10545-010-9212-5. Epub 2010 Oct 6. J Inherit Metab Dis. 2010. PMID: 20924685

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