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Genetics of cardiovascular disease
Citations 231-240 of 492 total displayed.
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Past content
(since Jan 1999):
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- Articles
SCN5A Mutation Associated With Dilated Cardiomyopathy, Conduction Disorder, and Arrhythmia
- William P. McNair, Lisa Ku, Matthew R.G. Taylor, Pam R. Fain, Dmi Dao, Eugene Wolfel, Luisa Mestroni and the Familial Cardiomyopathy Registry Research Group
Circulation published October 4, 2004, doi:10.1161/01.CIR.0000144458.58660.BB
[Abstract]
- Articles
Atherosclerosis in Patients Infected With HIV Is Influenced by a Mutant Monocyte Chemoattractant Protein-1 Allele
- Carlos Alonso-Villaverde, Blai Coll, Sandra Parra, Manuel Montero, Nahum Calvo, Mònica Tous, Jorge Joven, and Lluis Masana
Circulation published October 4, 2004, doi:10.1161/01.CIR.0000143835.95029.7D
[Abstract]
- Correspondence
Polymorphism of Inhibitory Renin-Angiotensin System as a Genetic Risk Factor for Atrial Fibrillation • Response
- Akiyoshi Ogimoto, Jitsuo Higaki, Tetsuro Miki, Chia-Ti Tsai, Ling-Ping Lai, Jiunn-Lee Lin, Fu-Tien Chiang, Juey-Jen Hwang, Kuan-Lih Hsu, Chuen-Den Tseng, Chiau-Suong Liau, Yung-Zu Tseng, Marylyn D. Ritchie, and Jason H. Moore
Circulation 2004;110:e329, doi:10.1161/01.CIR.0000142882.58972.51
[Full text]
- Basic Science for Clinicians
Genetic Basis of Atherosclerosis: Part I: New Genes and Pathways
- Aldons J. Lusis, Alan M. Fogelman, and Gregg C. Fonarow
Circulation 2004;110:1868-1873, doi:10.1161/01.CIR.0000143041.58692.CC
[Full text]
- Correspondence
Do Meta-Analyses of Association Studies of Endothelial Nitric Oxide Synthase Variants and Ischemic Heart Disease Provide Conclusive Answers? • Response
- Gian Paolo Rossi, Giuseppe Maiolino, Juan P. Casas, Aroon D. Hingorani, Steve E. Humphries, Liam Smeeth, and Leonelo E. Bautista
Circulation 2004;110:e305-306e, doi:10.1161/01.CIR.0000142057.63388.A6
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- Editorials
Cholesteryl Ester Transfer Protein and Coronary Artery Disease: An Observation With Therapeutic Implications
- Megan L. Wolfe and Daniel J. Rader
Circulation 2004;110:1338-1340, doi:10.1161/01.CIR.0000143047.52724.BB
[Full text]
- Vascular Medicine
Homozygous Deficiency of Heparin Cofactor II: Relevance of P17 Glutamate Residue in Serpins, Relationship With Conformational Diseases, and Role in Thrombosis
- Javier Corral, Justo Aznar, Rocio Gonzalez-Conejero, Piedad Villa, Antonia Miñano, Amparo Vayá, Robin W. Carrell, James A. Huntington, and Vicente Vicente
Circulation 2004;110:1303-1307; published online before print as doi:10.1161/01.CIR.0000140763.51679.D9
[Abstract]
[Full text]
- Articles
Homozygous Deficiency of Heparin Cofactor II. Relevance of P17 Glutamate Residue in Serpins, Relationship With Conformational Diseases, and Role in Thrombosis
- Javier Corral, Justo Aznar, Rocio Gonzalez-Conejero, Piedad Villa, Antonia Miñano, Amparo Vayá, Robin W. Carrell, James A. Huntington, and Vicente Vicente
Circulation published August 30, 2004, doi:10.1161/01.CIR.0000140763.51679.D9
[Abstract]
- Correspondence
Further Confirmation That a Conduction Disturbance Underlies the Electrocardiographic Pattern of the So-Called Brugada Syndrome • Response
- Bortolo Martini, Hanno L. Tan, Raymond Tukkie, Jim Vleugels, Irma K.L.M. de Groot, Arthur A.M. Wilde, and Peter Sogaard
Circulation 2004;110:e53, doi:10.1161/01.CIR.0000141260.46251.0E
[Full text]
- Correspondence
Genetic Variability of von Willebrand Factor and Atherosclerosis
- Frank W.G. Leebeek, Irene M. van der Meer, and Jacqueline C.M. Witteman
Circulation 2004;110:e57, doi:10.1161/01.cir.0000141263.99616.d9
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