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Clinical genetics
Citations 51-60 of 397 total displayed.
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Past content
(since Feb 1999):
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- Articles
Long-QT Syndrome After Age 40
- Ilan Goldenberg, Arthur J. Moss, James Bradley, Slava Polonsky, Derick R. Peterson, Scott McNitt, Wojciech Zareba, Mark L. Andrews, Jennifer L. Robinson, Michael J. Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Emanuela H. Locati, Carlo Napolitano, Silvia G. Priori, Ming Qi, Peter J. Schwartz, Jeffrey A. Towbin, G. Michael Vincent, and Li Zhang
Circulation published April 21, 2008, doi:10.1161/CIRCULATIONAHA.107.729368
[Abstract]
- Articles
Risk Factors for Aborted Cardiac Arrest and Sudden Cardiac Death in Children With the Congenital Long-QT Syndrome
- Ilan Goldenberg, Arthur J. Moss, Derick R. Peterson, Scott McNitt, Wojciech Zareba, Mark L. Andrews, Jennifer L. Robinson, Emanuela H. Locati, Michael J. Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Carlo Napolitano, Silvia G. Priori, Ming Qi, Peter J. Schwartz, Jeffrey A. Towbin, G. Michael Vincent, and Li Zhang
Circulation published April 21, 2008, doi:10.1161/CIRCULATIONAHA.107.701243
[Abstract]
- Editorials
Elucidating the Genetic Basis of Peripheral Arterial Disease: Identification of a Quantitative Trait Locus That Determines the Phenotypic Response to Experimental Hindlimb Ischemia
- Louis M. Messina
Circulation 2008;117:1127-1129, doi:10.1161/CIRCULATIONAHA.107.752055
[Full text]
- Genetics
Genetic Variation Within Adrenergic Pathways Determines In Vivo Effects of Presynaptic Stimulation in Humans
- Maple M. Fung, Carie Nguyen, Parag Mehtani, Rany M. Salem, Brandon Perez, Brenda Thomas, Madhusudan Das, Nicholas J. Schork, Sushil K. Mahata, Michael G. Ziegler, and Daniel T. O’Connor
Circulation 2008;117:517-525; published online before print as doi:10.1161/CIRCULATIONAHA.107.706317
[Abstract]
[Full text]
- Editorials
Modulating Phenotypic Expression of the PRKAG2 Cardiac Syndrome
- Michael H. Gollob
Circulation 2008;117:134-135, doi:10.1161/CIRCULATIONAHA.107.747345
[Full text]
- Aortic Diseases
Aortic Aneurysms: An Immune Disease With a Strong Genetic Component
- Helena Kuivaniemi, Chris D. Platsoucas, and M. David Tilson, III
Circulation 2008;117:242-252, doi:10.1161/CIRCULATIONAHA.107.690982
[Full text]
- Editorials
A Bold, New Initiative for Circulation: A Family of Subspecialty Journals
- Joseph Loscalzo
Circulation 2008;117:4-5, doi:10.1161/CIRCULATIONAHA.107.755710
[Full text]
- Arrhythmia/Electrophysiology
Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene (GPD1-L) Mutations in Sudden Infant Death Syndrome
- David W. Van Norstrand, Carmen R. Valdivia, David J. Tester, Kazuo Ueda, Barry London, Jonathan C. Makielski, and Michael J. Ackerman
Circulation 2007;116:2253-2259; published online before print as doi:10.1161/CIRCULATIONAHA.107.704627
[Abstract]
[Full text]
- Basic Science for Clinicians
Inherited Arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases Workshop Consensus Report About the Diagnosis, Phenotyping, Molecular Mechanisms, and Therapeutic Approaches for Primary Cardiomyopathies of Gene Mutations Affecting Ion Channel Function
- Stephan E. Lehnart, Michael J. Ackerman, D. Woodrow Benson, Jr, Ramon Brugada, Colleen E. Clancy, J. Kevin Donahue, Alfred L. George, Jr, Augustus O. Grant, Stephen C. Groft, Craig T. January, David A. Lathrop, W. Jonathan Lederer, Jonathan C. Makielski, Peter J. Mohler, Arthur Moss, Jeanne M. Nerbonne, Timothy M. Olson, Dennis A. Przywara, Jeffrey A. Towbin, Lan-Hsiang Wang, and Andrew R. Marks
Circulation 2007;116:2325-2345, doi:10.1161/CIRCULATIONAHA.107.711689
[Abstract]
[Full text]
- Articles
Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene (GPD1-L) Mutations in Sudden Infant Death Syndrome
- David W. Van Norstrand, Carmen R. Valdivia, David J. Tester, Kazuo Ueda, Barry London, Jonathan C. Makielski, and Michael J. Ackerman
Circulation published October 29, 2007, doi:10.1161/CIRCULATIONAHA.107.704627
[Abstract]
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