Roberts R - Search Results

1

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: roberts r. N Engl J Med. 1998 Apr 30;338(18):1248-57. doi: 10.1056/NEJM199804303381802. N Engl J Med. 1998. PMID: 9562578 Free article.

2

Angiotensin-I converting enzyme genotypes and left ventricular hypertrophy in patients with hypertrophic cardiomyopathy.

Lechin M, Quiñones MA, Omran A, Hill R, Yu QT, Rakowski H, Wigle D, Liew CC, Sole M, Roberts R, et al. Lechin M, et al. Among authors: roberts r. Circulation. 1995 Oct 1;92(7):1808-12. doi: 10.1161/01.cir.92.7.1808. Circulation. 1995. PMID: 7671365

3

Isolation of a de novo mutant myocardial beta MHC protein in a pedigree with hypertrophic cardiomyopathy.

Greve G, Bachinski L, Friedman DL, Czernuzewicz G, Anan R, Towbin J, Seidman CE, Roberts R. Greve G, et al. Among authors: roberts r. Hum Mol Genet. 1994 Nov;3(11):2073-5. Hum Mol Genet. 1994. PMID: 7874131 No abstract available.

4

Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscle.

Yu QT, Ifegwu J, Marian AJ, Mares A Jr, Hill R, Perryman MB, Bachinski LL, Roberts R. Yu QT, et al. Among authors: roberts r. Circulation. 1993 Feb;87(2):406-12. doi: 10.1161/01.cir.87.2.406. Circulation. 1993. PMID: 8425289

5

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA. Bowles KR, et al. Among authors: roberts r. J Clin Invest. 1996 Sep 15;98(6):1355-60. doi: 10.1172/JCI118922. J Clin Invest. 1996. PMID: 8823300 Free PMC article.

6

Genetic heterogeneity in familial dilated cardiomyopathy.

Schultz KR, Gajarski RJ, Pignatelli R, Goytia V, Roberts R, Bachinski L, Towbin JA. Schultz KR, et al. Among authors: roberts r. Biochem Mol Med. 1995 Dec;56(2):87-93. doi: 10.1006/bmme.1995.1061. Biochem Mol Med. 1995. PMID: 8825069

7

Familial hypertrophic cardiomyopathy: diagnostic and therapeutic implications of recent genetic studies.

Bachinski LL, Roberts R. Bachinski LL, et al. Among authors: roberts r. Mol Med Today. 1996 Sep;2(9):387-93. doi: 10.1016/s1357-4310(96)10030-7. Mol Med Today. 1996. PMID: 8885258 Review.

8

Molecular genetics of hypertrophic cardiomyopathy.

Roberts R, Marian AJ, Bachinski L. Roberts R, et al. J Card Fail. 1996 Dec;2(4 Suppl):S87-95. doi: 10.1016/s1071-9164(96)80063-7. J Card Fail. 1996. PMID: 8951565 Review. No abstract available.

9

Identification of a genetic locus for familial atrial fibrillation.

Brugada R, Tapscott T, Czernuszewicz GZ, Marian AJ, Iglesias A, Mont L, Brugada J, Girona J, Domingo A, Bachinski LL, Roberts R. Brugada R, et al. Among authors: roberts r. N Engl J Med. 1997 Mar 27;336(13):905-11. doi: 10.1056/NEJM199703273361302. N Engl J Med. 1997. PMID: 9070470 Free article.

10

Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathies.

Bachinski LL, Abchee A, Durand JB, Roberts R, Krahe R, Hobson GM. Bachinski LL, et al. Among authors: roberts r. Mol Cell Probes. 1997 Feb;11(1):55-8. doi: 10.1006/mcpr.1996.0076. Mol Cell Probes. 1997. PMID: 9076715

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