Liu TT - Search Results

1

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

2

A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.

Tsai PC, Soong BW, Mademan I, Huang YH, Liu CR, Hsiao CT, Wu HT, Liu TT, Liu YT, Tseng YT, Lin KP, Yang UC, Chung KW, Choi BO, Nicholson GA, Kennerson ML, Chan CC, De Jonghe P, Cheng TH, Liao YC, Züchner S, Baets J, Lee YC. Tsai PC, et al. Among authors: liu tt, liu yt, liu cr. Brain. 2017 May 1;140(5):1252-1266. doi: 10.1093/brain/awx058. Brain. 2017. PMID: 28369220 Free PMC article.

3

Mutations in KCND3 cause spinocerebellar ataxia type 22.

Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW. Lee YC, et al. Among authors: liu tt, liu yc. Ann Neurol. 2012 Dec;72(6):859-69. doi: 10.1002/ana.23701. Ann Neurol. 2012. PMID: 23280837 Free PMC article.

4

Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease.

Soong BW, Huang YH, Tsai PC, Huang CC, Pan HC, Lu YC, Chien HJ, Liu TT, Chang MH, Lin KP, Tu PH, Kao LS, Lee YC. Soong BW, et al. Among authors: liu tt. Am J Hum Genet. 2013 Mar 7;92(3):422-30. doi: 10.1016/j.ajhg.2013.01.014. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434117 Free PMC article.

5

Generation and analysis of the expressed sequence tags from the mycelium of Ganoderma lucidum.

Huang YH, Wu HY, Wu KM, Liu TT, Liou RF, Tsai SF, Shiao MS, Ho LT, Tzean SS, Yang UC. Huang YH, et al. Among authors: liu tt. PLoS One. 2013 May 2;8(5):e61127. doi: 10.1371/journal.pone.0061127. Print 2013. PLoS One. 2013. PMID: 23658685 Free PMC article.

6

The roles of alcohol dehydrogenase in patients with atrial fibrillation.

Hu YF, Chang YT, Lin YJ, Chang SL, Lo LW, Huang YH, Liu TT, Chen CH, Tuan TC, Chao TF, Chung FP, Liao JN, Te ALD, Huang CF, Chen SA. Hu YF, et al. Among authors: liu tt. Pacing Clin Electrophysiol. 2017 Dec;40(12):1446-1453. doi: 10.1111/pace.13208. Epub 2017 Oct 31. Pacing Clin Electrophysiol. 2017. PMID: 28975638

7

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

8

Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.

Lin MW, Lee DD, Liu TT, Lin YF, Chen SY, Huang CC, Weng HY, Liu YF, Tanaka A, Arita K, Lai-Cheong J, Palisson F, Chang YT, Wong CK, Matsuura I, McGrath JA, Tsai SF. Lin MW, et al. Among authors: liu tt, liu yf. Eur J Hum Genet. 2010 Jan;18(1):26-32. doi: 10.1038/ejhg.2009.135. Eur J Hum Genet. 2010. PMID: 19690585 Free PMC article.

9

Haploinsufficiency of RCBTB1 is associated with Coats disease and familial exudative vitreoretinopathy.

Wu JH, Liu JH, Ko YC, Wang CT, Chung YC, Chu KC, Liu TT, Chao HM, Jiang YJ, Chen SJ, Chung MY. Wu JH, et al. Among authors: liu tt, liu jh. Hum Mol Genet. 2016 Apr 15;25(8):1637-47. doi: 10.1093/hmg/ddw041. Epub 2016 Feb 11. Hum Mol Genet. 2016. PMID: 26908610

10

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.

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