Ingles J - Search Results

1

Establishment of an Australian National Genetic Heart Disease Registry.

Ingles J, McGaughran J, Vohra J, Weintraub RG, Davis A, Atherton J, Semsarian C. Ingles J, et al. Heart Lung Circ. 2008 Dec;17(6):463-7. doi: 10.1016/j.hlc.2008.05.603. Epub 2008 Aug 21. Heart Lung Circ. 2008. PMID: 18722159

2

Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy.

Jayatilleke I, Doolan A, Ingles J, McGuire M, Booth V, Richmond DR, Semsarian C. Jayatilleke I, et al. Among authors: ingles j. Am J Cardiol. 2004 May 1;93(9):1192-4. doi: 10.1016/j.amjcard.2004.01.057. Am J Cardiol. 2004. PMID: 15110224

3

Progression of left ventricular hypertrophy and the angiotensin-converting enzyme gene polymorphism in hypertrophic cardiomyopathy.

Doolan G, Nguyen L, Chung J, Ingles J, Semsarian C. Doolan G, et al. Among authors: ingles j. Int J Cardiol. 2004 Aug;96(2):157-63. doi: 10.1016/j.ijcard.2004.05.003. Int J Cardiol. 2004. PMID: 15314809

4

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: ingles j. 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

5

Long-term follow-up of patients with obstructive hypertrophic cardiomyopathy treated with dual-chamber pacing.

Megevand A, Ingles J, Richmond DR, Semsarian C. Megevand A, et al. Among authors: ingles j. Am J Cardiol. 2005 Apr 15;95(8):991-3. doi: 10.1016/j.amjcard.2004.12.045. Am J Cardiol. 2005. PMID: 15820173

6

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.

Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C. Ingles J, et al. J Med Genet. 2005 Oct;42(10):e59. doi: 10.1136/jmg.2005.033886. J Med Genet. 2005. PMID: 16199542 Free PMC article.

7

Sudden cardiac death in the young: a clinical genetic approach.

Ingles J, Semsarian C. Ingles J, et al. Intern Med J. 2007 Jan;37(1):32-7. doi: 10.1111/j.1445-5994.2006.01241.x. Intern Med J. 2007. PMID: 17199842 Review.

8

Mutation analysis of the natriuretic peptide precursor B (NPPB) gene in patients with hypertrophic cardiomyopathy.

Chiu C, Ingles J, Lind JM, Semsarian C. Chiu C, et al. Among authors: ingles j. DNA Seq. 2006 Oct;17(5):392-5. doi: 10.1080/10425170600724998. DNA Seq. 2006. PMID: 17343213

9

Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians.

Doolan A, Langlois N, Chiu C, Ingles J, Lind JM, Semsarian C. Doolan A, et al. Among authors: ingles j. Int J Cardiol. 2008 Jun 23;127(1):138-41. doi: 10.1016/j.ijcard.2007.05.001. Epub 2007 Jun 4. Int J Cardiol. 2008. PMID: 17544529

10

Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy.

Chiu C, Tebo M, Ingles J, Yeates L, Arthur JW, Lind JM, Semsarian C. Chiu C, et al. Among authors: ingles j. J Mol Cell Cardiol. 2007 Sep;43(3):337-43. doi: 10.1016/j.yjmcc.2007.06.009. Epub 2007 Jun 30. J Mol Cell Cardiol. 2007. PMID: 17655857

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