Lam L - Search Results

1

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.

Bagnall RD, Crompton DE, Petrovski S, Lam L, Cutmore C, Garry SI, Sadleir LG, Dibbens LM, Cairns A, Kivity S, Afawi Z, Regan BM, Duflou J, Berkovic SF, Scheffer IE, Semsarian C. Bagnall RD, et al. Among authors: lam l. Ann Neurol. 2016 Apr;79(4):522-34. doi: 10.1002/ana.24596. Epub 2016 Feb 2. Ann Neurol. 2016. PMID: 26704558

2

Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

Doolan A, Tebo M, Ingles J, Nguyen L, Tsoutsman T, Lam L, Chiu C, Chung J, Weintraub RG, Semsarian C. Doolan A, et al. Among authors: lam l. J Mol Cell Cardiol. 2005 Feb;38(2):387-93. doi: 10.1016/j.yjmcc.2004.12.006. Epub 2005 Jan 27. J Mol Cell Cardiol. 2005. PMID: 15698845

3

Genes, calcium and modifying factors in hypertrophic cardiomyopathy.

Tsoutsman T, Lam L, Semsarian C. Tsoutsman T, et al. Among authors: lam l. Clin Exp Pharmacol Physiol. 2006 Jan-Feb;33(1-2):139-45. doi: 10.1111/j.1440-1681.2006.04340.x. Clin Exp Pharmacol Physiol. 2006. PMID: 16445713 Review.

4

Application of proteomics in cardiovascular medicine.

Lam L, Lind J, Semsarian C. Lam L, et al. Int J Cardiol. 2006 Mar 22;108(1):12-9. doi: 10.1016/j.ijcard.2006.01.002. Epub 2006 Feb 8. Int J Cardiol. 2006. PMID: 16466817 Review.

5

Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy.

Tsoutsman T, Chung J, Doolan A, Nguyen L, Williams IA, Tu E, Lam L, Bailey CG, Rasko JE, Allen DG, Semsarian C. Tsoutsman T, et al. Among authors: lam l. J Mol Cell Cardiol. 2006 Oct;41(4):623-32. doi: 10.1016/j.yjmcc.2006.07.016. Epub 2006 Sep 1. J Mol Cell Cardiol. 2006. PMID: 16950368

6

Proteome map of the normal murine ventricular myocardium.

Lam L, Arthur J, Semsarian C. Lam L, et al. Proteomics. 2007 Oct;7(19):3629-33. doi: 10.1002/pmic.200700312. Proteomics. 2007. PMID: 17722207

7

Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy.

Tsoutsman T, Kelly M, Ng DC, Tan JE, Tu E, Lam L, Bogoyevitch MA, Seidman CE, Seidman JG, Semsarian C. Tsoutsman T, et al. Among authors: lam l. Circulation. 2008 Apr 8;117(14):1820-31. doi: 10.1161/CIRCULATIONAHA.107.755777. Epub 2008 Mar 24. Circulation. 2008. PMID: 18362229

8

Differential protein expression profiling of myocardial tissue in a mouse model of hypertrophic cardiomyopathy.

Lam L, Tsoutsman T, Arthur J, Semsarian C. Lam L, et al. J Mol Cell Cardiol. 2010 May;48(5):1014-22. doi: 10.1016/j.yjmcc.2009.08.015. Epub 2009 Aug 26. J Mol Cell Cardiol. 2010. PMID: 19715700

9

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia.

Gray B, Bagnall RD, Lam L, Ingles J, Turner C, Haan E, Davis A, Yang PC, Clancy CE, Sy RW, Semsarian C. Gray B, et al. Among authors: lam l. Heart Rhythm. 2016 Aug;13(8):1652-60. doi: 10.1016/j.hrthm.2016.05.004. Epub 2016 May 5. Heart Rhythm. 2016. PMID: 27157848 Free PMC article.

10

A Prospective Study of Sudden Cardiac Death among Children and Young Adults.

Bagnall RD, Weintraub RG, Ingles J, Duflou J, Yeates L, Lam L, Davis AM, Thompson T, Connell V, Wallace J, Naylor C, Crawford J, Love DR, Hallam L, White J, Lawrence C, Lynch M, Morgan N, James P, du Sart D, Puranik R, Langlois N, Vohra J, Winship I, Atherton J, McGaughran J, Skinner JR, Semsarian C. Bagnall RD, et al. Among authors: lam l. N Engl J Med. 2016 Jun 23;374(25):2441-52. doi: 10.1056/NEJMoa1510687. N Engl J Med. 2016. PMID: 27332903 Free article.

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