Seidman JG - Search Results

1

Gene mutations in apical hypertrophic cardiomyopathy.

Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE. Arad M, et al. Among authors: seidman jg, seidman ce. Circulation. 2005 Nov 1;112(18):2805-11. doi: 10.1161/CIRCULATIONAHA.105.547448. Circulation. 2005. PMID: 16267253

2

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

3

An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.

MacRae CA, Watkins HC, Jarcho JA, Thierfelder L, McKenna WJ, Seidman JG, Seidman CE. MacRae CA, et al. Among authors: seidman jg, seidman ce. Circulation. 1994 Jan;89(1):33-5. doi: 10.1161/01.cir.89.1.33. Circulation. 1994. PMID: 8281665

4

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.

5

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.

6

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.

Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE. Niimura H, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1998 Apr 30;338(18):1248-57. doi: 10.1056/NEJM199804303381802. N Engl J Med. 1998. PMID: 9562578 Free article.

7

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.

8

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

9

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy.

Ho CY, Lever HM, DeSanctis R, Farver CF, Seidman JG, Seidman CE. Ho CY, et al. Among authors: seidman jg, seidman ce. Circulation. 2000 Oct 17;102(16):1950-5. doi: 10.1161/01.cir.102.16.1950. Circulation. 2000. PMID: 11034944

10

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.

Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, McDonough B, Smoot L, Mullen MP, Woolf PK, Wigle ED, Seidman JG, Seidman CE. Kamisago M, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 2000 Dec 7;343(23):1688-96. doi: 10.1056/NEJM200012073432304. N Engl J Med. 2000. PMID: 11106718 Free article.

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