Seidman JG - Search Results

1

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.

Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG, et al. Watkins H, et al. Among authors: seidman jg. N Engl J Med. 1995 Apr 20;332(16):1058-64. doi: 10.1056/NEJM199504203321603. N Engl J Med. 1995. PMID: 7898523 Free article.

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

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

4

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Among authors: seidman jg, seidman ce. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

5

Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.

Watkins H, Thierfelder L, Anan R, Jarcho J, Matsumori A, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 1993 Dec;53(6):1180-5. Am J Hum Genet. 1993. PMID: 8250038 Free PMC article.

6

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

7

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.

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

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.

10

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.

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