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Clinical genetics
Citations 11-20 of 38 total displayed.
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Past content
(since Mar 2000):
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- Articles
Mechanisms of Abnormal Calcium Homeostasis in Mutations Responsible for Catecholaminergic Polymorphic Ventricular Tachycardia
- Vivek Iyer, Roger J. Hajjar, and Antonis A. Armoundas
Circ. Res. published January 18, 2007, doi:10.1161/01.RES.0000258468.31815.42
[Abstract]
- Clinical Research
Haplotypes of the Caspase-1 Gene, Plasma Caspase-1 Levels, and Cardiovascular Risk
- Stefan Blankenberg, Tiphaine Godefroy, Odette Poirier, Hans J. Rupprecht, Sandrine Barbaux, Christoph Bickel, Viviane Nicaud, Renate Schnabel, Frank Kee, Caroline Morrison, Alun Evans, Karl J. Lackner, François Cambien, Thomas Münzel, Laurence Tiret for the AtheroGene Investigators
Circ. Res. 2006;99:102-108; published online before print as doi:10.1161/01.RES.0000232324.87983.4b
[Abstract]
[Full text]
- Articles
Haplotypes of the Caspase-1 Gene, Plasma Caspase-1 Levels, and Cardiovascular Risk
- Stefan Blankenberg, Tiphaine Godefroy, Odette Poirier, Hans J. Rupprecht, Sandrine Barbaux, Christoph Bickel, Viviane Nicaud, Renate Schnabel, Frank Kee, Caroline Morrison, Alun Evans, Karl J. Lackner, François Cambien, Thomas Münzel, Laurence Tiret for the AtheroGene Investigators
Circ. Res. published June 15, 2006, doi:10.1161/01.RES.0000232324.87983.4b
[Abstract]
- Editorials
Intracellular Calcium Handling Dysfunction and Arrhythmogenesis: A New Challenge for the Electrophysiologist
- Silvia G. Priori and Carlo Napolitano
Circ. Res. 2005;97:1077-1079, doi:10.1161/01.RES.0000194556.41865.e2
[Full text]
- UltraRapid Communications
Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor
- Marina Cerrone, Barbara Colombi, Massimo Santoro, Marina Raffaele di Barletta, Mario Scelsi, Laura Villani, Carlo Napolitano, and Silvia G Priori
Circ. Res. 2005;96:e77-82e; published online before print as doi:10.1161/01.RES.0000169067.51055.72
[Abstract]
[Full text]
- Articles
Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor (RyR2)
- Marina Cerrone, Barbara Colombi, Massimo Santoro, Marina Raffale di Barletta, Mario Scelsi, Laura Villani, Carlo Napolitano, and Silvia G Priori
Circ. Res. published May 12, 2005, doi:10.1161/01.RES.0000169067.51055.72
[Abstract]
- Clinical Research
A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene
- Silvia G. Priori, Sandeep V. Pandit, Ilaria Rivolta, Omer Berenfeld, Elena Ronchetti, Amit Dhamoon, Carlo Napolitano, Justus Anumonwo, Marina Raffaele di Barletta, Smitha Gudapakkam, Giuliano Bosi, Marco Stramba-Badiale, and José Jalife
Circ. Res. 2005;96:800-807; published online before print as doi:10.1161/01.RES.0000162101.76263.8c
[Abstract]
[Full text]
- Articles
A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene
- Silvia G. Priori, Sandeep V. Pandit, Ilaria Rivolta, Omer Berenfeld, Elena Ronchetti, Amit Dhamoon, Carlo Napolitano, Justus Anumonwo, Marina Raffaele di Barletta, Smitha Gudapakkam, Giuliano Bosi, Marco Stramba-Badiale, and José Jalife
Circ. Res. published March 10, 2005, doi:10.1161/01.RES.0000162101.76263.8c
[Abstract]
- UltraRapid Communications
Association of Human Connexin40 Gene Polymorphisms With Atrial Vulnerability as a Risk Factor for Idiopathic Atrial Fibrillation
- Mehran Firouzi, Hemanth Ramanna, Bart Kok, Habo J. Jongsma, Bobby P.C. Koeleman, Pieter A. Doevendans, W. Antoinette Groenewegen, and Richard N.W. Hauer
Circ. Res. 2004;95:e29-33e; published online before print as doi:10.1161/01.RES.0000141134.64811.0a
[Abstract]
[Full text]
- Articles
Association of Human Connexin40 Gene Polymorphisms With Atrial Vulnerability as a Risk Factor for Idiopathic Atrial Fibrillation
- Mehran Firouzi, Hemanth Ramanna, Bart Kok, Habo J. Jongsma, Bobby P.C. Koeleman, Pieter A. Doevendans, W. Antoinette Groenewegen, and Richard N.W. Hauer
Circ. Res. published August 5, 2004, doi:10.1161/01.RES.0000141134.64811.0a
[Abstract]
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