Hsiao KJ - 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: hsiao kj. 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. Among authors: hsiao kj. 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

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: hsiao kj. 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

Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiency.

Chiang SH, Wu KF, Liu TT, Wu SJ, Hsiao KJ. Chiang SH, et al. Among authors: hsiao kj. Southeast Asian J Trop Med Public Health. 2003;34 Suppl 3:130-4. Southeast Asian J Trop Med Public Health. 2003. PMID: 15906716

5

Long-term follow-up of Taiwanese Chinese patients treated early for 6-pyruvoyl-tetrahydropterin synthase deficiency.

Liu KM, Liu TT, Lee NC, Cheng LY, Hsiao KJ, Niu DM. Liu KM, et al. Among authors: hsiao kj. Arch Neurol. 2008 Mar;65(3):387-92. doi: 10.1001/archneur.65.3.387. Arch Neurol. 2008. PMID: 18332253 Clinical Trial.

6

Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria.

Liu MY, Yang YL, Chang YC, Chiang SH, Lin SP, Han LS, Qi Y, Hsiao KJ, Liu TT. Liu MY, et al. Among authors: hsiao kj. J Hum Genet. 2010 Sep;55(9):621-6. doi: 10.1038/jhg.2010.81. Epub 2010 Jul 15. J Hum Genet. 2010. PMID: 20631720

7

Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients.

Liu MY, Liu TT, Yang YL, Chang YC, Fan YL, Lee SF, Teng YT, Chiang SH, Niu DM, Lin SJ, Chao MC, Lin SP, Han LS, Qi Y, Hsiao KJ. Liu MY, et al. Among authors: hsiao kj. JIMD Rep. 2012;6:55-64. doi: 10.1007/8904_2011_117. Epub 2012 Jan 31. JIMD Rep. 2012. PMID: 23430940 Free PMC article.

8

Neonatal screening and monitoring system in Taiwan.

Hwu WL, Huang AC, Chen JS, Hsiao KJ, Tsai WY. Hwu WL, et al. Among authors: hsiao kj. Southeast Asian J Trop Med Public Health. 2003;34 Suppl 3:91-3. Southeast Asian J Trop Med Public Health. 2003. PMID: 15906707

9

Long-term follow-up of Chinese patients who received delayed treatment for 6-pyruvoyl-tetrahydropterin synthase deficiency.

Lee NC, Cheng LY, Liu TT, Hsiao KJ, Chiu PC, Niu DM. Lee NC, et al. Among authors: hsiao kj. Mol Genet Metab. 2006 Feb;87(2):128-34. doi: 10.1016/j.ymgme.2005.09.028. Epub 2005 Dec 20. Mol Genet Metab. 2006. PMID: 16364672

10

Two frequent mutations associated with the classic form of propionic acidemia in Taiwan.

Chiu YH, Liu YN, Liao WL, Chang YC, Lin SP, Hsu CC, Chiu PC, Niu DM, Wang CH, Ke YY, Chien YH, Hsiao KJ, Liu TT. Chiu YH, et al. Among authors: hsiao kj. Biochem Genet. 2014 Oct;52(9-10):415-29. doi: 10.1007/s10528-014-9657-6. Epub 2014 May 27. Biochem Genet. 2014. PMID: 24863100

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