Chou YY - 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: chou hc, chou yy. Pediatr Crit Care Med. 2019 Nov;20(11):1021-1026. doi: 10.1097/PCC.0000000000002068. Pediatr Crit Care Med. 2019. PMID: 31261230

2

Russell-Silver syndrome: molecular diagnosis of maternal uniparental disomy of chromosome 7 using methylation-specific polymerase chain reaction assay and single nucleotide polymorphisms genotyping.

Chou YY, Chen CC, Kuo PL, Tsai WH, Lin SJ. Chou YY, et al. J Formos Med Assoc. 2004 Oct;103(10):797-802. J Formos Med Assoc. 2004. PMID: 15490033

3

Hypophosphatemic rickets associated with epidermal nevus syndrome and giant hairy nevus.

Chou YY, Chao SC, Shiue CN, Tsai WH, Lin SJ. Chou YY, et al. J Pediatr Endocrinol Metab. 2005 Jan;18(1):93-5. doi: 10.1515/jpem.2005.18.1.93. J Pediatr Endocrinol Metab. 2005. PMID: 15679074

4

Relationship between umbilical cord blood insulin-like growth factors and anthropometry in term newborns.

Hung TY, Lin CC, Hwang YS, Lin SJ, Chou YY, Tsai WH. Hung TY, et al. Among authors: chou yy. Acta Paediatr Taiwan. 2008 Jan-Feb;49(1):19-23. Acta Paediatr Taiwan. 2008. PMID: 18581724

5

Measuring propionyl-CoA carboxylase activity in phytohemagglutinin stimulated lymphocytes using high performance liquid chromatography.

Liu YN, Liu TT, Fan YL, Niu DM, Chien YH, Chou YY, Lee NC, Hsiao KJ, Chiu YH. Liu YN, et al. Among authors: chou yy. Clin Chim Acta. 2016 Jan 30;453:13-20. doi: 10.1016/j.cca.2015.11.023. Epub 2015 Nov 24. Clin Chim Acta. 2016. PMID: 26620954

6

Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series.

Lin HY, Chuang CK, Wang CH, Chien YH, Wang YM, Tsai FJ, Chou YY, Lin SJ, Pan HP, Niu DM, Hwu WL, Ke YY, Lin SP. Lin HY, et al. Among authors: chou yy. Mol Genet Metab Rep. 2016 Apr 18;7:63-9. doi: 10.1016/j.ymgmr.2016.04.003. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27134829 Free PMC article.

7

Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012.

Lin HY, Chuang CK, Huang YH, Tu RY, Lin FJ, Lin SJ, Chiu PC, Niu DM, Tsai FJ, Hwu WL, Chien YH, Lin JL, Chou YY, Tsai WH, Chang TM, Lin SP. Lin HY, et al. Among authors: chou yy. Orphanet J Rare Dis. 2016 Jun 27;11(1):85. doi: 10.1186/s13023-016-0471-6. Orphanet J Rare Dis. 2016. PMID: 27349225 Free PMC article.

8

Functional independence of Taiwanese children with Prader-Willi syndrome.

Lee CL, Lin HY, Tsai LP, Chiu HC, Tu RY, Huang YH, Chien YH, Lee NC, Niu DM, Chao MC, Tsai FJ, Chou YY, Chuang CK, Lin SP. Lee CL, et al. Among authors: chou yy. Am J Med Genet A. 2018 Jun;176(6):1309-1314. doi: 10.1002/ajmg.a.38705. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696774

9

Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese.

Yu MH, Tsang MH, Lai S, Ho MS, Tse DML, Willis B, Kwong AK, Chou YY, Lin SP, Quinzii CM, Hwu WL, Chien YH, Kuo PL, Chan VC, Tsoi C, Chong SC, Rodenburg RJT, Smeitink J, Mak CC, Yeung KS, Fung JL, Lam W, Hui J, Lee NC, Fung CW, Chung BH. Yu MH, et al. Among authors: chou yy. NPJ Genom Med. 2019 Aug 5;4:18. doi: 10.1038/s41525-019-0091-x. eCollection 2019. NPJ Genom Med. 2019. PMID: 31396399 Free PMC article.

10

Earlier and higher dosing of alglucosidase alfa improve outcomes in patients with infantile-onset Pompe disease: Evidence from real-world experiences.

Chien YH, Tsai WH, Chang CL, Chiu PC, Chou YY, Tsai FJ, Wong SL, Lee NC, Hwu WL. Chien YH, et al. Among authors: chou yy. Mol Genet Metab Rep. 2020 Apr 29;23:100591. doi: 10.1016/j.ymgmr.2020.100591. eCollection 2020 Jun. Mol Genet Metab Rep. 2020. PMID: 32373469 Free PMC article.

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