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Genetics of cardiovascular disease
Citations 381-390 of 491 total displayed.
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Past content
(since Jan 1999):
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- Clinical Investigations and Reports
Metavinculin Mutations Alter Actin Interaction in Dilated Cardiomyopathy
- Timothy M. Olson, Susanne Illenberger, Nina Y. Kishimoto, Stefan Huttelmaier, Mark T. Keating, and Brigitte M. Jockusch
Circulation 2002;105:431-437, doi:10.1161/hc0402.102930
[Abstract]
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- Clinical Investigations and Reports
Sarcomere Protein Gene Mutations in Hypertrophic Cardiomyopathy of the Elderly
- Hideshi Niimura, Kristen K. Patton, William J. McKenna, Johann Soults, Barry J. Maron, J.G. Seidman, and Christine E. Seidman
Circulation 2002;105:446-451, doi:10.1161/hc0402.102990
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- Clinical Investigations and Reports
Increased Risk of Arrhythmic Events in Long-QT Syndrome With Mutations in the Pore Region of the Human Ether-a-go-go–Related Gene Potassium Channel
- Arthur J. Moss, Wojciech Zareba, Elizabeth S. Kaufman, Eric Gartman, Derick R. Peterson, Jesaia Benhorin, Jeffrey A. Towbin, Mark T. Keating, Silvia G. Priori, Peter J. Schwartz, G. Michael Vincent, Jennifer L. Robinson, Mark L. Andrews BBS, Changyong Feng, W. Jackson Hall, Aharon Medina, Li Zhang, and Zhiqing Wang
Circulation published January 28, 2002, doi:10.1161/hc0702.105124
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- Articles
Fibrillin-1 Genotype Is Associated With
Aortic Stiffness and Disease Severity in Patients With Coronary
Artery Disease
- Tanya L. Medley, Timothy J. Cole, Christoph D. Gatzka, William Y.S. Wang, Anthony M. Dart, and Bronwyn A. Kingwell
Circulation published January 22, 2002, doi:10.1161/hc0702.104129
[Abstract]
- Clinical Investigations and Reports
Clinical, Genetic, and Biophysical Characterization of SCN5A Mutations Associated With Atrioventricular Conduction Block
- Dao W. Wang, Prakash C. Viswanathan, Jeffrey R. Balser, Alfred L. George, Jr, and D. Woodrow Benson
Circulation 2002;105:341-346, doi:10.1161/hc0302.102592
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- Correspondence
Consider Cardiomyopathy in Subjects With Familial Partial Lipodystrophy • Response
- Hartmut H.-J. Schmidt and Robert A. Hegele
Circulation 2002;105:e7
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- Articles
Clinical and Molecular Heterogeneity in the Brugada Syndrome. A Novel Gene Locus on Chromosome 3
- Raul Weiss, M. Michael Barmada, Tuduy Nguyen, Jolene S. Seibel, Doris Cavlovich, Cari A. Kornblit, Adam Angelilli, Flordeliza Villanueva, Dennis M. McNamara, and Barry London
Circulation published December 31, 2001, doi:10.1161/hc0602.103618
[Abstract]
- Clinical Investigations and Reports
Genetic Variation in Coagulation and Fibrinolytic Proteins and Their Relation With Acute Myocardial Infarction: A Systematic Review
- S. Matthijs Boekholdt, Nick R. Bijsterveld, Arno H.M. Moons, Marcel Levi, Harry R. Büller, and Ron J.G. Peters
Circulation 2001;104:3063-3068, doi:10.1161/hc5001.100793
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- Clinical Investigations and Reports
Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family
- Florence Kyndt, Vincent Probst, Franck Potet, Sophie Demolombe, Jean-Christophe Chevallier, Isabelle Baro, Jean-Paul Moisan, Pierre Boisseau, Jean-Jacques Schott, Denis Escande, and Hervé Le Marec
Circulation 2001;104:3081-3086, doi:10.1161/hc5001.100834
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- Correspondence
Anti-Ischemic Therapy and Myocardial Ischemia Shown by Single Photon Emission Computed Tomography Imaging
- Johann Auer, Robert Berent, Bernd Eber, Robert A. O’Rourke, Tuhin Chaudhuri, Leslee Shaw, and Daniel S. Berman
Circulation 2001;104:e151-152e
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