Seidman CE - Search Results

1

American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines.

Maron BJ, McKenna WJ, Danielson GK, Kappenberger LJ, Kuhn HJ, Seidman CE, Shah PM, Spencer WH 3rd, Spirito P, Ten Cate FJ, Wigle ED; American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents; European Society of Cardiology Committee for Practice Guidelines. Maron BJ, et al. Among authors: seidman ce. Eur Heart J. 2003 Nov;24(21):1965-91. doi: 10.1016/s0195-668x(03)00479-2. Eur Heart J. 2003. PMID: 14585256 No abstract available.

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

Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Watkins H, Seidman CE, MacRae C, Seidman JG, McKenna W. Watkins H, et al. Among authors: seidman jg, seidman ce. Br Heart J. 1992 Jan;67(1):34-8. doi: 10.1136/hrt.67.1.34. Br Heart J. 1992. PMID: 1739523 Free PMC article. Review. No abstract available.

5

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

Jarcho JA, McKenna W, Pare JA, Solomon SD, Holcombe RF, Dickie S, Levi T, Donis-Keller H, Seidman JG, Seidman CE. Jarcho JA, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1989 Nov 16;321(20):1372-8. doi: 10.1056/NEJM198911163212005. N Engl J Med. 1989. PMID: 2811944

6

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1995 Dec;11(4):434-7. doi: 10.1038/ng1295-434. Nat Genet. 1995. PMID: 7493025

7

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

8

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

9

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.

10

A dinucleotide repeat polymorphism in the human LAMB2 gene on chromosome 1q.

Watkins HC, MacRae CA, Thierfelder L, McKenna WJ, Seidman CE, Seidman JG. Watkins HC, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 1993 Jul;2(7):1084. doi: 10.1093/hmg/2.7.1084-a. Hum Mol Genet. 1993. PMID: 8364561 No abstract available.

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