Chang CY - Search Results

1

Functional independence of Taiwanese patients with mucopolysaccharidoses.

Lee CL, Lin HY, Chuang CK, Chiu HC, Tu RY, Huang YH, Hwu WL, Tsai FJ, Chiu PC, Niu DM, Chen YJ, Chao MC, Chang TM, Lin JL, Chang CY, Kao YC, Lin SP. Lee CL, et al. Among authors: chang tm, chang cy. Mol Genet Genomic Med. 2019 Aug;7(8):e790. doi: 10.1002/mgg3.790. Epub 2019 Jun 18. Mol Genet Genomic Med. 2019. PMID: 31215158 Free PMC article.

2

Cri-du-chat syndrome.

Chang CY, Lin SP, Lin HY, Chen YJ, Kao HA, Yeung CY, Hsu CH, Chi H. Chang CY, et al. Acta Paediatr Taiwan. 2007 Nov-Dec;48(6):328-31. Acta Paediatr Taiwan. 2007. PMID: 18437967

3

Non-ketotic hyperglycinemia with a novel GLDC mutation in a Taiwanese child.

Chang CY, Lin SP, Lin HY, Chuang CK, Ho CS, Hsu CH. Chang CY, et al. Acta Paediatr Taiwan. 2008 Jan-Feb;49(1):35-7. Acta Paediatr Taiwan. 2008. PMID: 18581728

4

X-linked myotubular myopathy with a novel MTM1 mutation in a Taiwanese child.

Chang CY, Lin SP, Lin HY, Chuang CK, Ho CS, Su YN. Chang CY, et al. J Formos Med Assoc. 2008 Dec;107(12):965-70. doi: 10.1016/S0929-6646(09)60022-X. J Formos Med Assoc. 2008. PMID: 19129059 Free article.

5

Intravenous pamidronate therapy in Taiwanese patients with osteogenesis imperfecta.

Lin HY, Lin SP, Chuang CK, Chen MR, Chang CY. Lin HY, et al. Among authors: chang cy. Pediatr Neonatol. 2008 Oct;49(5):161-5. doi: 10.1016/S1875-9572(09)60002-4. Pediatr Neonatol. 2008. PMID: 19133566 Free article.

6

Clinical features of osteogenesis imperfecta in Taiwan.

Lin HY, Lin SP, Chuang CK, Chen MR, Chang CY, Niu DM. Lin HY, et al. Among authors: chang cy. J Formos Med Assoc. 2009 Jul;108(7):570-6. doi: 10.1016/S0929-6646(09)60375-2. J Formos Med Assoc. 2009. PMID: 19586831 Free article.

7

A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan.

Lin SP, Lin HY, Wang TJ, Chang CY, Lin CH, Huang SF, Tsai CC, Liu HL, Keutzer J, Chuang CK. Lin SP, et al. Among authors: chang cy. Orphanet J Rare Dis. 2013 Sep 22;8:147. doi: 10.1186/1750-1172-8-147. Orphanet J Rare Dis. 2013. PMID: 24053568 Free PMC article.

8

Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI.

Lin HY, Chuang CK, Chen MR, Lin SM, Hung CL, Chang CY, Chiu PC, Tsai WH, Niu DM, Tsai FJ, Lin SJ, Hwu WL, Lin JL, Lin SP. Lin HY, et al. Among authors: chang cy. Mol Genet Metab. 2016 Apr;117(4):431-7. doi: 10.1016/j.ymgme.2016.02.003. Epub 2016 Feb 16. Mol Genet Metab. 2016. PMID: 26899310

9

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.

Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP. Lin HY, et al. Among authors: chang cy. Mol Genet Metab. 2016 Sep;119(1-2):8-13. doi: 10.1016/j.ymgme.2016.07.003. Epub 2016 Jul 12. Mol Genet Metab. 2016. PMID: 27436784

10

An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan.

Lin HY, Lee CL, Lo YT, Tu RY, Chang YH, Chang CY, Chiu PC, Chang TM, Tsai WH, Niu DM, Chuang CK, Lin SP. Lin HY, et al. Among authors: chang yh, chang tm, chang cy. Diagnostics (Basel). 2019 Oct 5;9(4):140. doi: 10.3390/diagnostics9040140. Diagnostics (Basel). 2019. PMID: 31590383 Free PMC article.

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