Hershberger RE - Search Results

1

Peters S, Johnson R, Birch S, Zentner D, Hershberger RE, Fatkin D. Peters S, et al. Among authors: hershberger re. Heart Lung Circ. 2020 Apr;29(4):566-574. doi: 10.1016/j.hlc.2019.11.018. Epub 2019 Dec 17. Heart Lung Circ. 2020. PMID: 31974027 Review.

2

Differences in beta-adrenergic neuroeffector mechanisms in ischemic versus idiopathic dilated cardiomyopathy.

Bristow MR, Anderson FL, Port JD, Skerl L, Hershberger RE, Larrabee P, O'Connell JB, Renlund DG, Volkman K, Murray J, et al. Bristow MR, et al. Among authors: hershberger re. Circulation. 1991 Sep;84(3):1024-39. doi: 10.1161/01.cir.84.3.1024. Circulation. 1991. PMID: 1653120

3

Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected.

Hershberger RE, Ni H, Crispell KA. Hershberger RE, et al. J Card Fail. 1999 Sep;5(3):203-12. doi: 10.1016/s1071-9164(99)90005-2. J Card Fail. 1999. PMID: 10496193

4

Periodic rescreening is indicated for family members at risk of developing familial dilated cardiomyopathy.

Crispell KA, Hanson EL, Coates K, Toy W, Hershberger RE. Crispell KA, et al. Among authors: hershberger re. J Am Coll Cardiol. 2002 May 1;39(9):1503-7. doi: 10.1016/s0735-1097(02)01788-6. J Am Coll Cardiol. 2002. PMID: 11985914 Free article.

5

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.

Hershberger RE, Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Litt M. Hershberger RE, et al. Am Heart J. 2002 Dec;144(6):1081-6. doi: 10.1067/mhj.2002.126737. Am Heart J. 2002. PMID: 12486434

6

Clinical and genetic issues in familial dilated cardiomyopathy.

Burkett EL, Hershberger RE. Burkett EL, et al. Among authors: hershberger re. J Am Coll Cardiol. 2005 Apr 5;45(7):969-81. doi: 10.1016/j.jacc.2004.11.066. J Am Coll Cardiol. 2005. PMID: 15808750 Free article. Review.

7

Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.

Kushner JD, Nauman D, Burgess D, Ludwigsen S, Parks SB, Pantely G, Burkett E, Hershberger RE. Kushner JD, et al. Among authors: hershberger re. J Card Fail. 2006 Aug;12(6):422-9. doi: 10.1016/j.cardfail.2006.03.009. J Card Fail. 2006. PMID: 16911908

8

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, Hershberger RE. Parks SB, et al. Among authors: hershberger re. Am Heart J. 2008 Jul;156(1):161-9. doi: 10.1016/j.ahj.2008.01.026. Epub 2008 Mar 12. Am Heart J. 2008. PMID: 18585512 Free PMC article.

9

Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Hershberger RE, Cowan J, Morales A, Siegfried JD. Hershberger RE, et al. Circ Heart Fail. 2009 May;2(3):253-61. doi: 10.1161/CIRCHEARTFAILURE.108.817346. Circ Heart Fail. 2009. PMID: 19808347 Free PMC article. Review.

10

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.

Hershberger RE, Pinto JR, Parks SB, Kushner JD, Li D, Ludwigsen S, Cowan J, Morales A, Parvatiyar MS, Potter JD. Hershberger RE, et al. Circ Cardiovasc Genet. 2009 Aug;2(4):306-13. doi: 10.1161/CIRCGENETICS.108.846733. Epub 2009 May 15. Circ Cardiovasc Genet. 2009. PMID: 20031601 Free PMC article.

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