Liu CS - Search Results

1

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions.

Chung WH, Chang WC, Lee YS, Wu YY, Yang CH, Ho HC, Chen MJ, Lin JY, Hui RC, Ho JC, Wu WM, Chen TJ, Wu T, Wu YR, Hsih MS, Tu PH, Chang CN, Hsu CN, Wu TL, Choon SE, Hsu CK, Chen DY, Liu CS, Lin CY, Kaniwa N, Saito Y, Takahashi Y, Nakamura R, Azukizawa H, Shi Y, Wang TH, Chuang SS, Tsai SF, Chang CJ, Chang YS, Hung SI; Taiwan Severe Cutaneous Adverse Reaction Consortium; Japan Pharmacogenomics Data Science Consortium. Chung WH, et al. Among authors: liu cs. JAMA. 2014 Aug 6;312(5):525-34. doi: 10.1001/jama.2014.7859. JAMA. 2014. PMID: 25096692

2

Long-term follow-up of spinal and bulbar muscular atrophy in Taiwan.

Fu SC, Kuo HC, Chu CC, Wu YR, Ro LS, Liu CS, Huang CC. Fu SC, et al. Among authors: liu cs. J Formos Med Assoc. 2013 Jun;112(6):326-31. doi: 10.1016/j.jfma.2012.03.008. Epub 2012 Jun 6. J Formos Med Assoc. 2013. PMID: 23787009 Free article.

3

Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome.

Chen CH, Chen TH, Kuo SJ, Chen CP, Lee DJ, Ke YY, Yeh KT, Ma GC, Liu CS, Shih JC, Chen M. Chen CH, et al. Among authors: liu cs. Lymphology. 2009 Sep;42(3):134-8. Lymphology. 2009. PMID: 19927903 Review.

4

SCA31 is rare in the Chinese population on Taiwan.

Lee YC, Liu CS, Lee TY, Lo YC, Lu YC, Soong BW. Lee YC, et al. Among authors: liu cs. Neurobiol Aging. 2012 Feb;33(2):426.e23-4. doi: 10.1016/j.neurobiolaging.2010.10.012. Epub 2010 Dec 15. Neurobiol Aging. 2012. PMID: 21163552

5

Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report.

Ou YH, Chen AW, Fan JY, Cheng WL, Lin TT, Chen MK, Liu CS. Ou YH, et al. Among authors: liu cs. Medicine (Baltimore). 2018 Oct;97(42):e12878. doi: 10.1097/MD.0000000000012878. Medicine (Baltimore). 2018. PMID: 30335006 Free PMC article.

6

Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.

Chiang MC, Chen HM, Lee YH, Chang HH, Wu YC, Soong BW, Chen CM, Wu YR, Liu CS, Niu DM, Wu JY, Chen YT, Chern Y. Chiang MC, et al. Among authors: liu cs. Hum Mol Genet. 2007 Mar 1;16(5):483-98. doi: 10.1093/hmg/ddl481. Epub 2007 Jan 9. Hum Mol Genet. 2007. PMID: 17213233

7

Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax.

Yeang CH, Ma GC, Shih JC, Yang YS, Chen CP, Chang SP, Wu SH, Liu CS, Kuo SJ, Chou HC, Hwu WL, Cameron AD, Ginsberg NA, Lin YS, Chen M. Yeang CH, et al. Among authors: liu cs. PLoS One. 2012;7(4):e34901. doi: 10.1371/journal.pone.0034901. Epub 2012 Apr 18. PLoS One. 2012. PMID: 22529953 Free PMC article.

8

Caveolin-1 provides palliation for adverse hepatic reactions in hypercholesterolemic rabbits.

Chen YH, Lin WW, Liu CS, Hsu LS, Lin YM, Su SL. Chen YH, et al. Among authors: liu cs. PLoS One. 2014 Jan 24;9(1):e71862. doi: 10.1371/journal.pone.0071862. eCollection 2014. PLoS One. 2014. PMID: 24475013 Free PMC article.

9

A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy.

Ma GC, Liu CS, Chang SP, Yeh KT, Ke YY, Chen TH, Wang BB, Kuo SJ, Shih JC, Chen M. Ma GC, et al. Among authors: liu cs. Prenat Diagn. 2008 Nov;28(11):1057-63. doi: 10.1002/pd.2130. Prenat Diagn. 2008. PMID: 18973153

10

Mitochondrial dysfunction and psychiatric disorders.

Jou SH, Chiu NY, Liu CS. Jou SH, et al. Among authors: liu cs. Chang Gung Med J. 2009 Jul-Aug;32(4):370-9. Chang Gung Med J. 2009. PMID: 19664343 Free article. Review.

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