Bahl A - Search Results

1

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

Mogensen J, Murphy RT, Kubo T, Bahl A, Moon JC, Klausen IC, Elliott PM, McKenna WJ. Mogensen J, et al. Among authors: bahl a. J Am Coll Cardiol. 2004 Dec 21;44(12):2315-25. doi: 10.1016/j.jacc.2004.05.088. J Am Coll Cardiol. 2004. PMID: 15607392 Free article.

2

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.

Mogensen J, Murphy RT, Shaw T, Bahl A, Redwood C, Watkins H, Burke M, Elliott PM, McKenna WJ. Mogensen J, et al. Among authors: bahl a. J Am Coll Cardiol. 2004 Nov 16;44(10):2033-40. doi: 10.1016/j.jacc.2004.08.027. J Am Coll Cardiol. 2004. PMID: 15542288 Free article.

3

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.

Murphy RT, Mogensen J, McGarry K, Bahl A, Evans A, Osman E, Syrris P, Gorman G, Farrell M, Holton JL, Hanna MG, Hughes S, Elliott PM, Macrae CA, McKenna WJ. Murphy RT, et al. Among authors: bahl a. J Am Coll Cardiol. 2005 Mar 15;45(6):922-30. doi: 10.1016/j.jacc.2004.11.053. J Am Coll Cardiol. 2005. PMID: 15766830 Free article.

4

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.

Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ. Kubo T, et al. Among authors: bahl a. J Am Coll Cardiol. 2007 Jun 26;49(25):2419-26. doi: 10.1016/j.jacc.2007.02.061. Epub 2007 Jun 11. J Am Coll Cardiol. 2007. PMID: 17599605 Free article.

5

Hypertrophic cardiomyopathy-the clinical challenge of managing a hereditary heart condition.

Mogensen J, Bahl A, McKenna WJ. Mogensen J, et al. Among authors: bahl a. Eur Heart J. 2003 Mar;24(6):496-8. doi: 10.1016/s0195-668x(02)00815-1. Eur Heart J. 2003. PMID: 12643880 No abstract available.

6

Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy.

Mogensen J, Bahl A, Kubo T, Elanko N, Taylor R, McKenna WJ. Mogensen J, et al. Among authors: bahl a. J Med Genet. 2003 May;40(5):e59. doi: 10.1136/jmg.40.5.e59. J Med Genet. 2003. PMID: 12746413 Free PMC article. No abstract available.

7

Familial conduction system disease associated with hypertrophic cardiomyopathy.

Bahl A, Saikia UN, Talwar KK. Bahl A, et al. Int J Cardiol. 2008 Apr 25;125(3):e44-7. doi: 10.1016/j.ijcard.2006.12.050. Epub 2007 Apr 18. Int J Cardiol. 2008. PMID: 17445920

8

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.

Rai TS, Ahmad S, Bahl A, Ahuja M, Ahluwalia TS, Singh B, Talwar KK, Khullar M. Rai TS, et al. Among authors: bahl a. Mol Cell Biochem. 2009 Jan;321(1-2):189-96. doi: 10.1007/s11010-008-9932-0. Epub 2008 Oct 25. Mol Cell Biochem. 2009. PMID: 18953637

9

Mitochondrial DNA variations associated with hypertrophic cardiomyopathy.

Govindaraj P, Khan NA, Rani B, Rani DS, Selvaraj P, Jyothi V, Bahl A, Narasimhan C, Rakshak D, Premkumar K, Khullar M, Thangaraj K. Govindaraj P, et al. Among authors: bahl a. Mitochondrion. 2014 May;16:65-72. doi: 10.1016/j.mito.2013.10.006. Epub 2013 Nov 9. Mitochondrion. 2014. PMID: 24215792

10

Genetic and clinical profile of Indian patients of idiopathic restrictive cardiomyopathy with and without hypertrophy.

Rai TS, Ahmad S, Ahluwalia TS, Ahuja M, Bahl A, Saikia UN, Singh B, Talwar KK, Khullar M. Rai TS, et al. Among authors: bahl a. Mol Cell Biochem. 2009 Nov;331(1-2):187-92. doi: 10.1007/s11010-009-0157-7. Epub 2009 May 17. Mol Cell Biochem. 2009. PMID: 19449150

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