Chiang CC - Search Results

1

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: chiang cc. 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.

2

High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese population.

Lin HY, Chong KW, Hsu JH, Yu HC, Shih CC, Huang CH, Lin SJ, Chen CH, Chiang CC, Ho HJ, Lee PC, Kao CH, Cheng KH, Hsueh C, Niu DM. Lin HY, et al. Among authors: chiang cc. Circ Cardiovasc Genet. 2009 Oct;2(5):450-6. doi: 10.1161/CIRCGENETICS.109.862920. Epub 2009 Jul 24. Circ Cardiovasc Genet. 2009. PMID: 20031620

3

Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan.

Niu DM, Chien YH, Chiang CC, Ho HC, Hwu WL, Kao SM, Chiang SH, Kao CH, Liu TT, Chiang H, Hsiao KJ. Niu DM, et al. Among authors: chiang cc, chiang sh, chiang h. J Inherit Metab Dis. 2010 Oct;33(Suppl 2):S295-305. doi: 10.1007/s10545-010-9129-z. Epub 2010 Jun 22. J Inherit Metab Dis. 2010. PMID: 20567911

4

Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan.

Liao HC, Chiang CC, Niu DM, Wang CH, Kao SM, Tsai FJ, Huang YH, Liu HC, Huang CK, Gao HJ, Yang CF, Chan MJ, Lin WD, Chen YJ. Liao HC, et al. Among authors: chiang cc. Clin Chim Acta. 2014 Apr 20;431:80-6. doi: 10.1016/j.cca.2014.01.030. Epub 2014 Feb 7. Clin Chim Acta. 2014. PMID: 24513544

5

Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI.

Chan MJ, Liao HC, Gelb MH, Chuang CK, Liu MY, Chen HJ, Kao SM, Lin HY, Huang YH, Kumar AB, Chennamaneni NK, Pendem N, Lin SP, Chiang CC. Chan MJ, et al. Among authors: chiang cc. J Pediatr. 2019 Feb;205:176-182. doi: 10.1016/j.jpeds.2018.09.063. Epub 2018 Nov 6. J Pediatr. 2019. PMID: 30409495 Free PMC article.

6

Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A).

Lin HY, Huang CH, Yu HC, Chong KW, Hsu JH, Lee PC, Cheng KH, Chiang CC, Ho HJ, Lin SP, Chen SJ, Lin PK, Niu DM. Lin HY, et al. Among authors: chiang cc. J Inherit Metab Dis. 2010 Oct;33(5):619-24. doi: 10.1007/s10545-010-9166-7. Epub 2010 Sep 7. J Inherit Metab Dis. 2010. PMID: 20821055

7

A large-scale nationwide newborn screening program for Pompe disease in Taiwan: towards effective diagnosis and treatment.

Yang CF, Liu HC, Hsu TR, Tsai FC, Chiang SF, Chiang CC, Ho HC, Lai CJ, Yang TF, Chuang SY, Lin CY, Niu DM. Yang CF, et al. Among authors: chiang cc, chiang sf. Am J Med Genet A. 2014 Jan;164A(1):54-61. doi: 10.1002/ajmg.a.36197. Epub 2013 Nov 15. Am J Med Genet A. 2014. PMID: 24243590

8

Clinical observations on enzyme replacement therapy in patients with Fabry disease and the switch from agalsidase beta to agalsidase alfa.

Lin HY, Huang YH, Liao HC, Liu HC, Hsu TR, Shen CI, Li ST, Li CF, Lee LH, Lee PC, Huang CK, Chiang CC, Lin SP, Niu DM. Lin HY, et al. Among authors: chiang cc. J Chin Med Assoc. 2014 Apr;77(4):190-7. doi: 10.1016/j.jcma.2013.11.006. Epub 2013 Dec 30. J Chin Med Assoc. 2014. PMID: 24388678 Free article.

9

Mass Spectrometry but Not Fluorimetry Distinguishes Affected and Pseudodeficiency Patients in Newborn Screening for Pompe Disease.

Liao HC, Chan MJ, Yang CF, Chiang CC, Niu DM, Huang CK, Gelb MH. Liao HC, et al. Among authors: chiang cc. Clin Chem. 2017 Jul;63(7):1271-1277. doi: 10.1373/clinchem.2016.269027. Epub 2017 Apr 27. Clin Chem. 2017. PMID: 28450385 Free PMC article.

10

Functional and biological studies of α-galactosidase A variants with uncertain significance from newborn screening in Taiwan.

Liao HC, Hsu TR, Young L, Chiang CC, Huang CK, Liu HC, Niu DM, Chen YJ. Liao HC, et al. Among authors: chiang cc. Mol Genet Metab. 2018 Feb;123(2):140-147. doi: 10.1016/j.ymgme.2017.06.002. Epub 2017 Jun 8. Mol Genet Metab. 2018. PMID: 28615118

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