Liu TT - 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: liu tt, liu my. 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: liu tt, liu my. 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: liu tt. 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: liu tt. 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: liu tt. Arch Neurol. 2008 Mar;65(3):387-92. doi: 10.1001/archneur.65.3.387. Arch Neurol. 2008. PMID: 18332253 Clinical Trial.

6

Brain damage by mild metabolic derangements in methylmalonic acidemia.

Lee NC, Chien YH, Peng SF, Huang AC, Liu TT, Wu AS, Chen LC, Hsu LW, Tseng SC, Hwu WL. Lee NC, et al. Among authors: liu tt. Pediatr Neurol. 2008 Nov;39(5):325-9. doi: 10.1016/j.pediatrneurol.2008.07.018. Pediatr Neurol. 2008. PMID: 18940555

7

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: liu tt. 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

8

Combined methylmalonic aciduria and homocystinuria cblC type of a Taiwanese infant with c.609G>A and C.567dupT mutations in the MMACHC gene.

Chang JT, Chen YY, Liu TT, Liu MY, Chiu PC. Chang JT, et al. Among authors: liu tt, liu my. Pediatr Neonatol. 2011 Aug;52(4):223-6. doi: 10.1016/j.pedneo.2011.05.006. Epub 2011 Jul 16. Pediatr Neonatol. 2011. PMID: 21835369 Free article.

9

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: liu tt. JIMD Rep. 2012;6:55-64. doi: 10.1007/8904_2011_117. Epub 2012 Jan 31. JIMD Rep. 2012. PMID: 23430940 Free PMC article.

10

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: liu tt. 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

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