Genetics of cardiovascular disease

Citations 461-470 of 491 total displayed.

Past content (since Jan 1999):

Clinical Investigations and Reports
Elevated HDL Cholesterol Is a Risk Factor for Ischemic Heart Disease in White Women When Caused by a Common Mutation in the Cholesteryl Ester Transfer Protein Gene

Birgit Agerholm-Larsen, Børge G. Nordestgaard, Rolf Steffensen, Gorm Jensen, and Anne Tybjærg-Hansen
Circulation 2000;101:1907-1912 [Abstract] [Full text]  

Clinical Investigations and Reports
Dilated Cardiomyopathy and Sensorineural Hearing Loss : A Heritable Syndrome That Maps to 6q23–24

Jost Schönberger, Hara Levy, Ekkehard Grünig, Somkiat Sangwatanaroj, Diane Fatkin, Calum MacRae, Hinrich Stäcker, Christopher Halpin, Roland Eavey, Edward F. Philbin, Hugo Katus, J. G. Seidman, and Christine E. Seidman
Circulation 2000;101:1812-1818 [Abstract] [Full text]  

Clinical Investigations and Reports
Effects of Flecainide in Patients With New SCN5A Mutation : Mutation-Specific Therapy for Long-QT Syndrome?

J. Benhorin, R. Taub, M. Goldmit, B. Kerem, R. S. Kass, I. Windman, and A. Medina
Circulation 2000;101:1698-1706 [Abstract] [Full text]  

Circulation Electronic Pages
Differences in Cardiac Energetics Between Patients With Familial and Nonfamilial Hypertrophic Cardiomyopathy

Wulf-Ingo Jung, Thomas Hoess, Michael Bunse, Stefan Widmaier, Ludger Sieverding, Johannes Breuer, Jürgen Apitz, Oliver Schmidt, Franz van Erckelens, Guenther J. Dietze, and Otto Lutz
Circulation 2000;101:e121 [Full text]  

Clinical Investigations and Reports
The Apolipoprotein 4 Allele Determines Prognosis and the Effect on Prognosis of Simvastatin in Survivors of Myocardial Infarction : A Substudy of the Scandinavian Simvastatin Survival Study

Lars Ulrik Gerdes, Christian Gerdes, Kari Kervinen, Markku Savolainen, Ib Christian Klausen, Peter Steen Hansen, Y. Antero Kesäniemi, and Ole Færgeman
Circulation 2000;101:1366-1371 [Abstract] [Full text]  

Clinical Investigations and Reports
A Newly Created Splice Donor Site in Exon 25 of the MyBP-C Gene Is Responsible for Inherited Hypertrophic Cardiomyopathy With Incomplete Disease Penetrance

Johannes A. Moolman, Sebastian Reith, Kerstin Uhl, Sonja Bailey, Mathias Gautel, Brigitte Jeschke, Christine Fischer, Julia Ochs, William J. McKenna, Heinz Klues, and Hans-Peter Vosberg
Circulation 2000;101:1396-1402 [Abstract] [Full text]  

Basic Science Reports
Cellular Arrhythmogenic Effects of Congenital and Acquired Long-QT Syndrome in the Heterogeneous Myocardium

Prakash C. Viswanathan and Yoram Rudy
Circulation 2000;101:1192-1198 [Abstract] [Full text]  

Basic Science Reports
Platelet GP IIIa Pl^A Polymorphisms Display Different Sensitivities to Agonists

Alan D. Michelson, Mark I. Furman, Pascal Goldschmidt-Clermont, Mary Ann Mascelli, Craig Hendrix, Lindsay Coleman, Jeanette Hamlington, Marc R. Barnard, Thomas Kickler, Douglas J. Christie, Sourav Kundu, and Paul F. Bray
Circulation 2000;101:1013-1018 [Abstract] [Full text]  

Brief Rapid Communications
Paraoxonase Polymorphism (Gln192Arg) as a Determinant of the Response of Human Coronary Arteries to Serotonin

Christophe Bauters, Carole Amant, Agnès Boulier, Philippe Cabrol, Eugène McFadden, Patrick Duriez, Michel E. Bertrand, and Philippe Amouyel
Circulation 2000;101:740-743 [Abstract] [Full text]  

Brief Rapid Communications
Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

Gary L. Brodsky, Francesco Muntoni, Snjezana Miocic, Gianfranco Sinagra, Caroline Sewry, and Luisa Mestroni
Circulation 2000;101:473-476 [Abstract] [Full text]  

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