Hershberger RE - Search Results

1

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.

2

Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice.

Crispell KA, Wray A, Ni H, Nauman DJ, Hershberger RE. Crispell KA, et al. Among authors: hershberger re. J Am Coll Cardiol. 1999 Sep;34(3):837-47. doi: 10.1016/s0735-1097(99)00276-4. J Am Coll Cardiol. 1999. PMID: 10483968 Free article.

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

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.

Jakobs PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, Hershberger RE. Jakobs PM, et al. Among authors: hershberger re. J Card Fail. 2001 Sep;7(3):249-56. doi: 10.1054/jcaf.2001.26339. J Card Fail. 2001. PMID: 11561226

5

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.

Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Dienel NH, Litt M, Hershberger RE. Hanson EL, et al. Among authors: hershberger re. J Card Fail. 2002 Feb;8(1):28-32. doi: 10.1054/jcaf.2002.31157. J Card Fail. 2002. PMID: 11862580

6

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.

7

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

8

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

9

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Li D, Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Partain J, Nixon RR, Allen CN, Irwin RP, Jakobs PM, Litt M, Hershberger RE. Li D, et al. Among authors: hershberger re. Am J Hum Genet. 2006 Dec;79(6):1030-9. doi: 10.1086/509900. Epub 2006 Oct 24. Am J Hum Genet. 2006. PMID: 17186461 Free PMC article.

10

The family history as a tool to identify patients at risk for dilated cardiomyopathy.

Nauman D, Morales A, Cowan J, Dagua J, Hershberger RE. Nauman D, et al. Among authors: hershberger re. Prog Cardiovasc Nurs. 2008 Winter;23(1):41-4. doi: 10.1111/j.1751-7117.2008.08223.x. Prog Cardiovasc Nurs. 2008. PMID: 18326985 Review. No abstract available.

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