Liu TT - Search Results

1

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

2

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.

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

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.

5

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: liu tt, liu yn. 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

6

Measuring propionyl-CoA carboxylase activity in phytohemagglutinin stimulated lymphocytes using high performance liquid chromatography.

Liu YN, Liu TT, Fan YL, Niu DM, Chien YH, Chou YY, Lee NC, Hsiao KJ, Chiu YH. Liu YN, et al. Among authors: liu tt. Clin Chim Acta. 2016 Jan 30;453:13-20. doi: 10.1016/j.cca.2015.11.023. Epub 2015 Nov 24. Clin Chim Acta. 2016. PMID: 26620954

7

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

8

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.

9

A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function.

Tsai PC, Huang YH, Guo YC, Wu HT, Lin KP, Tsai YS, Liao YC, Liu YT, Liu TT, Kao LS, Yet SF, Fann MJ, Soong BW, Lee YC. Tsai PC, et al. Among authors: liu tt, liu yt. Neurology. 2014 Sep 2;83(10):903-12. doi: 10.1212/WNL.0000000000000758. Epub 2014 Aug 6. Neurology. 2014. PMID: 25098539

10

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.

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