Lin DS - Search Results

1

Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004.

Lin HY, Lin SP, Chen YJ, Hsu CH, Kao HA, Chen MR, Hung HY, Ho CS, Chang JH, Huang FY, Tsai TC, Lin DS, Chan WT. Lin HY, et al. Among authors: lin sp, lin ds. Pediatr Int. 2007 Jun;49(3):380-6. doi: 10.1111/j.1442-200X.2007.02377.x. Pediatr Int. 2007. PMID: 17532840

2

Interference and blood sample preparation for a pyruvate enzymatic assay.

Chuang CK, Wang TJ, Yeung CY, Hsieh WS, Lin DS, Ho SC, Lin SP. Chuang CK, et al. Among authors: lin sp, lin ds. Clin Biochem. 2006 Jan;39(1):74-7. doi: 10.1016/j.clinbiochem.2005.10.007. Epub 2005 Nov 23. Clin Biochem. 2006. PMID: 16309664

3

Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers.

Lin SP, Chang JH, Lee-Chen GJ, Lin DS, Lin HY, Chuang CK. Lin SP, et al. Among authors: lin hy, lin ds. Clin Chim Acta. 2006 Jul 15;369(1):29-34. doi: 10.1016/j.cca.2006.01.001. Epub 2006 Feb 9. Clin Chim Acta. 2006. PMID: 16480701

4

Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004.

Lin HY, Lin SP, Chen YJ, Hung HY, Kao HA, Hsu CH, Chen MR, Chang JH, Ho CS, Huang FY, Shyur SD, Lin DS, Lee HC. Lin HY, et al. Among authors: lin sp, lin ds. Am J Med Genet A. 2006 May 1;140(9):945-51. doi: 10.1002/ajmg.a.31173. Am J Med Genet A. 2006. PMID: 16528742

5

A method for lactate and pyruvate determination in filter-paper dried blood spots.

Chuang CK, Wang TJ, Yeung CY, Lin DS, Lin HY, Liu HL, Ho HT, Hsieh WS, Lin SP. Chuang CK, et al. Among authors: lin hy, lin sp, lin ds. J Chromatogr A. 2009 Dec 18;1216(51):8947-52. doi: 10.1016/j.chroma.2009.10.074. Epub 2009 Oct 31. J Chromatogr A. 2009. PMID: 19913794

6

Polysomnographic characteristics in patients with mucopolysaccharidoses.

Lin HY, Chen MR, Lin CC, Chen CP, Lin DS, Chuang CK, Niu DM, Chang JH, Lee HC, Lin SP. Lin HY, et al. Among authors: lin sp, lin cc, lin ds. Pediatr Pulmonol. 2010 Dec;45(12):1205-12. doi: 10.1002/ppul.21309. Epub 2010 Aug 17. Pediatr Pulmonol. 2010. PMID: 20717914

7

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

8

A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a family.

Lin DS, Yeung CY, Liu HL, Ho CS, Shu CH, Chuang CK, Huang YW, Wu TY, Huang ZD, Jian YR, Lin SP. Lin DS, et al. Among authors: lin sp. Am J Med Genet A. 2011 Jun;155A(6):1285-9. doi: 10.1002/ajmg.a.33963. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567914

9

CNS-targeted AAV5 gene transfer results in global dispersal of vector and prevention of morphological and function deterioration in CNS of globoid cell leukodystrophy mouse model.

Lin DS, Hsiao CD, Liau I, Lin SP, Chiang MF, Chuang CK, Wang TJ, Wu TY, Jian YR, Huang SF, Liu HL. Lin DS, et al. Among authors: lin sp. Mol Genet Metab. 2011 Aug;103(4):367-77. doi: 10.1016/j.ymgme.2011.05.005. Epub 2011 May 12. Mol Genet Metab. 2011. PMID: 21620749

10

Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndrome.

Lin DS, Chang JH, Liu HL, Wei CH, Yeung CY, Ho CS, Shu CH, Chiang MF, Chuang CK, Huang YW, Wu TY, Jian YR, Huang ZD, Lin SP. Lin DS, et al. Among authors: lin sp. Am J Med Genet A. 2011 Dec;155A(12):3095-9. doi: 10.1002/ajmg.a.34326. Epub 2011 Nov 3. Am J Med Genet A. 2011. PMID: 22052856

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