Seidman CE - Search Results

1

The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet Study.

Ho CY, Day SM, Colan SD, Russell MW, Towbin JA, Sherrid MV, Canter CE, Jefferies JL, Murphy AM, Cirino AL, Abraham TP, Taylor M, Mestroni L, Bluemke DA, Jarolim P, Shi L, Sleeper LA, Seidman CE, Orav EJ; HCMNet Investigators. Ho CY, et al. Among authors: seidman ce. JAMA Cardiol. 2017 Apr 1;2(4):419-428. doi: 10.1001/jamacardio.2016.5670. JAMA Cardiol. 2017. PMID: 28241245 Free PMC article.

2

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

3

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Watkins H, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

4

A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.

Watkins H, Anan R, Coviello DA, Spirito P, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Circulation. 1995 May 1;91(9):2302-5. doi: 10.1161/01.cir.91.9.2302. Circulation. 1995. PMID: 7729014

5

Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene.

Solomon SD, Wolff S, Watkins H, Ridker PM, Come P, McKenna WJ, Seidman CE, Lee RT. Solomon SD, et al. Among authors: seidman ce. J Am Coll Cardiol. 1993 Aug;22(2):498-505. doi: 10.1016/0735-1097(93)90055-6. J Am Coll Cardiol. 1993. PMID: 8335820 Free article.

6

Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.

Watkins H, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 1995;4 Spec No:1721-7. doi: 10.1093/hmg/4.suppl_1.1721. Hum Mol Genet. 1995. PMID: 8541871 Review.

7

A mouse model of familial hypertrophic cardiomyopathy.

Geisterfer-Lowrance AA, Christe M, Conner DA, Ingwall JS, Schoen FJ, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Among authors: seidman jg, seidman ce. Science. 1996 May 3;272(5262):731-4. doi: 10.1126/science.272.5262.731. Science. 1996. PMID: 8614836

8

Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene.

Coviello DA, Maron BJ, Spirito P, Watkins H, Vosberg HP, Thierfelder L, Schoen FJ, Seidman JG, Seidman CE. Coviello DA, et al. Among authors: seidman jg, seidman ce. J Am Coll Cardiol. 1997 Mar 1;29(3):635-40. doi: 10.1016/s0735-1097(96)00538-4. J Am Coll Cardiol. 1997. PMID: 9060904 Free article.

9

Molecular genetic studies of familial hypertrophic cardiomyopathy.

Seidman CE, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Basic Res Cardiol. 1998;93 Suppl 3:13-6. doi: 10.1007/s003950050196. Basic Res Cardiol. 1998. PMID: 9879437 Review.

10

Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.

Gruver EJ, Fatkin D, Dodds GA, Kisslo J, Maron BJ, Seidman JG, Seidman CE. Gruver EJ, et al. Among authors: seidman jg, seidman ce. Am J Cardiol. 1999 Jun 17;83(12A):13H-18H. doi: 10.1016/s0002-9149(99)00251-9. Am J Cardiol. 1999. PMID: 10750581

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