Kao CH - 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: kao ch. 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

Growth hormone therapy in neonatal patients with methylmalonic acidemia.

Kao CH, Liu MY, Liu TT, Hsiao KJ, Cheng KH, Huang CH, Lin HY, Niu DM. Kao CH, et al. J Chin Med Assoc. 2009 Sep;72(9):462-7. doi: 10.1016/S1726-4901(09)70408-3. J Chin Med Assoc. 2009. PMID: 19762313 Free article.

3

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: kao ch. 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

4

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: kao sm, kao ch. 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

5

Lenticular subluxation in a patient with homocystinuria undetected by neonatal screening.

Cheng KH, Hung MC, Chen SJ, Kao CH, Niu DM. Cheng KH, et al. Among authors: kao ch. J Chin Med Assoc. 2007 Dec;70(12):562-4. doi: 10.1016/S1726-4901(08)70062-5. J Chin Med Assoc. 2007. PMID: 18194900 Free article.

6

Junctional epidermolysis bullosa.

Kao CH, Chen SJ, Hwang B, Yang AH, Hsu CY, Huang CH. Kao CH, et al. J Chin Med Assoc. 2006 Oct;69(10):503-6. doi: 10.1016/S1726-4901(09)70318-1. J Chin Med Assoc. 2006. PMID: 17098678 Free article.

7

Six new mutations of the thyroglobulin gene discovered in taiwanese children presenting with thyroid dyshormonogenesis.

Niu DM, Hsu JH, Chong KW, Huang CH, Lu YH, Kao CH, Yu HC, Lo MY, Jap TS. Niu DM, et al. Among authors: kao ch. J Clin Endocrinol Metab. 2009 Dec;94(12):5045-52. doi: 10.1210/jc.2009-0646. Epub 2009 Oct 16. J Clin Endocrinol Metab. 2009. PMID: 19837936

8

Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report.

Fu CH, Leung C, Kao CH, Yeh SJ. Fu CH, et al. Among authors: kao ch. J Formos Med Assoc. 2015 Aug;114(8):769-73. doi: 10.1016/j.jfma.2012.08.001. Epub 2012 Sep 7. J Formos Med Assoc. 2015. PMID: 26254176 Free article.

9

Glycogenic hepatopathy in type 1 diabetes mellitus.

Lin YC, Kao CH. Lin YC, et al. Among authors: kao ch. Liver Int. 2012 Sep;32(8):1294. doi: 10.1111/j.1478-3231.2012.02844.x. Epub 2012 Jun 25. Liver Int. 2012. PMID: 22731940 No abstract available.

10

Early diagnosis of Gitelman syndrome in a young child: A case report.

Wu CY, Tsai MH, Chen CC, Kao CH. Wu CY, et al. Among authors: kao ch. World J Clin Cases. 2022 Mar 26;10(9):2844-2850. doi: 10.12998/wjcc.v10.i9.2844. World J Clin Cases. 2022. PMID: 35434103 Free PMC article.

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