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Genetics of cardiovascular disease
Citations 421-430 of 492 total displayed.
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Past content
(since Jan 1999):
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- Clinical Investigations and Reports
Common Hepatic Lipase Gene Promoter Variant Determines Clinical Response to Intensive Lipid-Lowering Treatment
- Alberto Zambon, Samir S. Deeb, B. Greg Brown, John E. Hokanson, and John D. Brunzell
Circulation 2001;103:792-798
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- Clinical Investigations and Reports
Common Genetic Variation in ABCA1 Is Associated With Altered Lipoprotein Levels and a Modified Risk for Coronary Artery Disease
- Susanne M. Clee, Aeilko H. Zwinderman, James C. Engert, Karin Y. Zwarts, Henri O. F. Molhuizen, Kirsten Roomp, J. Wouter Jukema, Michel van Wijland, Marjel van Dam, Thomas J. Hudson, Angela Brooks-Wilson, Jacques Genest, Jr, John J. P. Kastelein, and Michael R. Hayden
Circulation 2001;0:13r-20r
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- Basic Science Reports
Right Ventricular Hypertrophy Secondary to Pulmonary Hypertension Is Linked to Rat Chromosome 17 : Evaluation of Cardiac Ryanodine Ryr2 Receptor as a Candidate
- Lan Zhao, Abdelkrim Sebkhi, Derek J. R. Nunez, Lu Long, Christopher S. Haley, Josiane Szpirer, Claude Szpirer, Alan J. Williams, and Martin R. Wilkins
Circulation 2001;103:442-447
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- Clinical Investigations and Reports
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia
- Silvia G. Priori, Carlo Napolitano, Natascia Tiso, Mirella Memmi, Gabriele Vignati, Raffaella Bloise, Vincenzo Sorrentino, and Gian Antonio Danieli
Circulation 2001;103:196-200
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- Editorials
Twenty-First Century Phox: Not Yet Ready for Widespread Screening
- Alexander Steven Whitehead and Garret A. FitzGerald
Circulation 2001;103:7-9
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- Clinical Investigations and Reports
Hypertrophic Cardiomyopathy Caused by a Novel  -Tropomyosin Mutation (V95A) Is Associated With Mild Cardiac Phenotype, Abnormal Calcium Binding to Troponin, Abnormal Myosin Cycling, and Poor Prognosis
- Akihiko Karibe, Larry S. Tobacman, James Strand, Carol Butters, Nick Back, Linda L. Bachinski, Andrew E. Arai, Anne Ortiz, Robert Roberts, Earl Homsher, and Lameh Fananapazir
Circulation 2001;103:65-71
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- Clinical Investigations and Reports
Genotype-Phenotype Correlation in the Long-QT Syndrome : Gene-Specific Triggers for Life-Threatening Arrhythmias
- Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini, Arthur J. Moss, G. Michael Vincent, Carlo Napolitano, Isabelle Denjoy, Pascale Guicheney, Günter Breithardt, Mark T. Keating, Jeffrey A. Towbin, Alan H. Beggs, Paul Brink, Arthur A. M. Wilde, Lauri Toivonen, Wojciech Zareba, Jennifer L. Robinson, Katherine W. Timothy, Valerie Corfield, Duangrurdee Wattanasirichaigoon, Clive Corbett, Wilhelm Haverkamp, Eric Schulze-Bahr, Michael H. Lehmann, Ketty Schwartz, Philippe Coumel, and Raffaella Bloise
Circulation 2001;103:89-95
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- Correspondence
Smoking and Aldosterone Synthase Polymorphism • Response
- Pitt O. Lim, Aarno Hautanen, M. Mänttäri, Markku Kupari, V. Manninen, Petri Toivanen, Leena Tenkanen, Kathleen M. Kayes, Scott Rosenfeld, and Perrin C. White
Circulation 2000;102:e183
[Full text]
- Clinical Investigations and Reports
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia
- Silvia G. Priori, Carlo Napolitano, Natascia Tiso, Mirella Memmi, Gabriele Vignati, Raffaella Bloise, Vincenzo Sorrentino, and Gian Antonio Danieli
Circulation 2000;0:11r
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- Editorials
Predicting the Long-QT Genotype From Clinical Data : From Sense to Science
- Arthur A. M. Wilde and Dan M. Roden
Circulation 2000;102:2796-2798
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