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Clinical genetics
Citations 201-210 of 397 total displayed.
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Past content
(since Feb 1999):
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- Arrhythmia/Electrophysiology
Transgenic Mouse Model of Ventricular Preexcitation and Atrioventricular Reentrant Tachycardia Induced by an AMP-Activated Protein Kinase Loss-of-Function Mutation Responsible for Wolff-Parkinson-White Syndrome
- Jasvinder S. Sidhu, Yadavendra S. Rajawat, Tapan G. Rami, Michael H. Gollob, Zhinong Wang, Ruiyong Yuan, A.J. Marian, Francesco J. DeMayo, Donald Weilbacher, George E. Taffet, Joanna K. Davies, David Carling, Dirar S. Khoury, and Robert Roberts
Circulation 2005;111:21-29; published online before print as doi:10.1161/01.CIR.0000151291.32974.D5
[Abstract]
[Full text]
- Arrhythmia/Electrophysiology
Genome-Wide Linkage Scan Identifies a Novel Genetic Locus on Chromosome 5p13 for Neonatal Atrial Fibrillation Associated With Sudden Death and Variable Cardiomyopathy
- Carlos Oberti, Lejin Wang, Lin Li, Jiamei Dong, Shaoqi Rao, Wei Du, and Qing Wang
Circulation 2004;110:3753-3759; published online before print as doi:10.1161/01.CIR.0000150333.87176.C7
[Abstract]
[Full text]
- Articles
Transgenic Mouse Model of Ventricular Preexcitation and Atrioventricular Reentrant Tachycardia Induced by an AMP-Activated Protein Kinase Loss-of-Function Mutation Responsible for Wolff-Parkinson-White Syndrome
- Jasvinder S. Sidhu, Yadavendra S. Rajawat, Tapan G. Rami, Michael H. Gollob, Zhinong Wang, Ruiyong Yuan, A. J. Marian, Francesco J. DeMayo, Donald Weilbacher, George E. Taffet, Joanna K. Davies, David Carling, Dirar S. Khoury, and Robert Roberts
Circulation published December 20, 2004, doi:10.1161/01.CIR.0000151291.32974.D5
[Abstract]
- Articles
Genome-Wide Linkage Scan Identifies a Novel Genetic Locus on Chromosome 5p13 for Neonatal Atrial Fibrillation Associated With Sudden Death and Variable Cardiomyopathy
- Carlos Oberti, Lejin Wang, Lin Li, Jiamei Dong, Shaoqi Rao, Wei Du, and Qing Wang
Circulation published December 13, 2004, doi:10.1161/01.CIR.0000150333.87176.C7
[Abstract]
- Editorials
Regenerating More Than Muscle in Muscular Dystrophy
- Ahlke Heydemann and Elizabeth M. McNally
Circulation 2004;110:3290-3292, doi:10.1161/01.CIR.0000149847.84152.0B
[Full text]
- Arrhythmia/Electrophysiology
Value of Electrocardiographic Parameters and Ajmaline Test in the Diagnosis of Brugada Syndrome Caused by SCN5A Mutations
- Kui Hong, Josep Brugada, Antonio Oliva, Antonio Berruezo-Sanchez, Domenico Potenza, Guido D. Pollevick, Alejandra Guerchicoff, Kiyotaka Matsuo, Elena Burashnikov, Robert Dumaine, Jeffrey A. Towbin, Vladislav Nesterenko, Pedro Brugada, Charles Antzelevitch, and Ramon Brugada
Circulation 2004;110:3023-3027; published online before print as doi:10.1161/01.CIR.0000144299.17008.07
[Abstract]
[Full text]
- Articles
Value of Electrocardiographic Parameters and Ajmaline Test in the Diagnosis of Brugada Syndrome Caused by SCN5A Mutations
- Kui Hong, Josep Brugada, Antonio Oliva, Antonio Berruezo-Sanchez, Domenico Potenza, Guido D. Pollevick, Alejandra Guerchicoff, Kiyotaka Matsuo, Elena Burashnikov, Robert Dumaine, Jeffrey A. Towbin, Vladislav Nesterenko, Pedro Brugada, Charles Antzelevitch, and Ramon Brugada
Circulation published November 1, 2004, doi:10.1161/01.CIR.0000144299.17008.07
[Abstract]
- Molecular Cardiology
Left Ventricular Mass in Relation to Genetic Variation in Angiotensin II Receptors, Renin System Genes, and Sodium Excretion
- Tatiana Kuznetsova, Jan A. Staessen, Lutgarde Thijs, Christiane Kunath, Agnieszka Olszanecka, Andrew Ryabikov, Valérie Tikhonoff, Katarzyna Stolarz, Giuseppe Bianchi, Edoardo Casiglia, Robert Fagard, Stefan-Martin Brand-Herrmann, Kalina Kawecka-Jaszcz, Sofia Malyutina, Yuri Nikitin, Eva Brand for the European Project On Genes in Hypertension Investigators
Circulation 2004;110:2644-2650; published online before print as doi:10.1161/01.CIR.0000145541.63406.BA
[Abstract]
[Full text]
- Articles
Left Ventricular Mass in Relation to Genetic Variation in Angiotensin II Receptors, Renin System Genes, and Sodium Excretion
- Tatiana Kuznetsova, Jan A. Staessen, Lutgarde Thijs, Christiane Kunath, Agnieszka Olszanecka, Andrew Ryabikov, Valérie Tikhonoff, Katarzyna Stolarz, Giuseppe Bianchi, Edoardo Casiglia, Robert Fagard, Stefan-Martin Brand-Herrmann, Kalina Kawecka-Jaszcz, Sofia Malyutina, Yuri Nikitin, Eva Brand for the European Project On Genes in Hypertension (EPOGH) Investigators
Circulation published October 18, 2004, doi:10.1161/01.CIR.0000145541.63406.BA
[Abstract]
- Editorials
Family History, Subclinical Atherosclerosis, and Coronary Heart Disease Risk: Barriers and Opportunities for the Use of Family History Information in Risk Prediction and Prevention
- Christopher J. O’Donnell
Circulation 2004;110:2074-2076, doi:10.1161/01.CIR.0000145539.77021.AC
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