Roberts R - Search Results

1

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations.

Marian AJ, Mares A Jr, Kelly DP, Yu QT, Abchee AB, Hill R, Roberts R. Marian AJ, et al. Among authors: roberts r. Eur Heart J. 1995 Mar;16(3):368-76. doi: 10.1093/oxfordjournals.eurheartj.a060920. Eur Heart J. 1995. PMID: 7789380

2

Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.

Marian AJ, Yu QT, Mares A Jr, Hill R, Roberts R, Perryman MB. Marian AJ, et al. Among authors: roberts r. J Clin Invest. 1992 Dec;90(6):2156-65. doi: 10.1172/JCI116101. J Clin Invest. 1992. PMID: 1361491 Free PMC article.

3

Accumulation and assembly of myosin in hypertrophic cardiomyopathy with the 403 Arg to Gln beta-myosin heavy chain mutation.

Vybiral T, Deitiker PR, Roberts R, Epstein HF. Vybiral T, et al. Among authors: roberts r. Circ Res. 1992 Dec;71(6):1404-9. doi: 10.1161/01.res.71.6.1404. Circ Res. 1992. PMID: 1423936

4

Molecular biology for the cardiologist.

Mares A Jr, Towbin J, Bies RD, Roberts R. Mares A Jr, et al. Among authors: roberts r. Curr Probl Cardiol. 1992 Jan;17(1):1-72. doi: 10.1016/0146-2806(92)90010-l. Curr Probl Cardiol. 1992. PMID: 1563272 Review. No abstract available.

5

Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy.

Perryman MB, Yu QT, Marian AJ, Mares A Jr, Czernuszewicz G, Ifegwu J, Hill R, Roberts R. Perryman MB, et al. Among authors: roberts r. J Clin Invest. 1992 Jul;90(1):271-7. doi: 10.1172/JCI115848. J Clin Invest. 1992. PMID: 1634614 Free PMC article.

6

Isolation of a human chromosome 14-only somatic cell hybrid: analysis using Alu and LINE-based PCR.

Mares A Jr, Ledbetter SA, Ledbetter DH, Roberts R, Hejtmancik JF. Mares A Jr, et al. Among authors: roberts r. Genomics. 1991 Sep;11(1):215-8. doi: 10.1016/0888-7543(91)90122-u. Genomics. 1991. PMID: 1765380

7

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population.

Hejtmancik JF, Brink PA, Towbin J, Hill R, Brink L, Tapscott T, Trakhtenbroit A, Roberts R. Hejtmancik JF, et al. Among authors: roberts r. Circulation. 1991 May;83(5):1592-7. doi: 10.1161/01.cir.83.5.1592. Circulation. 1991. PMID: 2022018

8

Early diagnosis of acute myocardial infarction based on assay for subforms of creatine kinase-MB.

Puleo PR, Guadagno PA, Roberts R, Scheel MV, Marian AJ, Churchill D, Perryman MB. Puleo PR, et al. Among authors: roberts r. Circulation. 1990 Sep;82(3):759-64. doi: 10.1161/01.cir.82.3.759. Circulation. 1990. PMID: 2203554

9

Molecular genetics: cardiac disease and risk-related genes.

Roberts R. Roberts R. Clin Cardiol. 1995 Sep;18(9 Suppl 4):IV13-9. doi: 10.1002/clc.4960181604. Clin Cardiol. 1995. PMID: 7489615 Free article. Review.

10

Molecular and clinical aspects of inherited cardiomyopathies.

Durand JB, Abchee AB, Roberts R. Durand JB, et al. Among authors: roberts r. Ann Med. 1995 Jun;27(3):311-7. doi: 10.3109/07853899509002583. Ann Med. 1995. PMID: 7546620 Free article. Review.

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