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Cardiology in Review
|
May 19, 2025
Myocardial Repair and Molecular Changes Following Mechanical Unloading With Ventricular Assist Device
Alaaeddine El Ghazawi, Hadi Skouri, Mohammad Sabra, et al.
Cardiac Electrophysiology Clinics
|
February 28, 2016
Iron Overload Leading to Torsades de Pointes in β-Thalassemia and Long QT Syndrome
Marwan M Refaat, Lea El Hage, Annette Buur Steffensen, et al.
Journal of the American College of Cardiology
|
December 3, 2021
Exercise-Induced Ventricular Ectopy and Cardiovascular Mortality in Asymptomatic Individuals
Marwan M Refaat, Charbel Gharios, M Vinayaga Moorthy, et al.
Acta Physiologica (Oxford, England)
|
August 28, 2020
Nicotinamide adenine dinucleotide: Biosynthesis, consumption and therapeutic role in cardiac diseases
Cynthia Tannous, George W Booz, Raffaele Altara, et al.
Journal of Cardiac Failure
|
February 4, 2012
Survival benefit of implantable cardioverter-defibrillators in left ventricular assist device-supported heart failure patients
Marwan M Refaat, Toshikazu Tanaka, Robert L Kormos, et al.
Pacing and Clinical Electrophysiology : PACE
|
July 15, 2015
The Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long QT Syndrome
Kristian L Poulsen, Mostafa Hotait, Kirstine Calloe, et al.
Critical Pathways in Cardiology
|
June 24, 2015
Obstructive Sleep Apnea and Atrial Fibrillation: Pathophysiology and Implications for Treatment
Abhishek Maan, Moussa Mansour, Elad Anter, et al.
Circulation Research
|
June 11, 2011
A novel ryanodine receptor mutation linked to sudden death increases sensitivity to cytosolic calcium
Albano C Meli, Marwan M Refaat, Miroslav Dura, et al.
Annals of Hematology
|
July 8, 2021
Digital thermography and vascular involvement in β-thalassemia intermedia
Farah Abdulhai, Miran A Jaffa, Joseph Elias, et al.
Circulation. Arrhythmia and Electrophysiology
|
February 21, 2013
Characterization and mechanisms of action of novel NaV1.5 channel mutations associated with Brugada syndrome
Kirstine Calloe, Marwan M Refaat, Soren Grubb, et al.
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of 13
Search research articles
Search
Showing results (91-100 of 125) with videos related to
Sort By:
Page
of 13
Cardiology in Review
|
May 19, 2025
Myocardial Repair and Molecular Changes Following Mechanical Unloading With Ventricular Assist Device
Alaaeddine El Ghazawi, Hadi Skouri, Mohammad Sabra, et al.
Cardiac Electrophysiology Clinics
|
February 28, 2016
Iron Overload Leading to Torsades de Pointes in β-Thalassemia and Long QT Syndrome
Marwan M Refaat, Lea El Hage, Annette Buur Steffensen, et al.
Journal of the American College of Cardiology
|
December 3, 2021
Exercise-Induced Ventricular Ectopy and Cardiovascular Mortality in Asymptomatic Individuals
Marwan M Refaat, Charbel Gharios, M Vinayaga Moorthy, et al.
Acta Physiologica (Oxford, England)
|
August 28, 2020
Nicotinamide adenine dinucleotide: Biosynthesis, consumption and therapeutic role in cardiac diseases
Cynthia Tannous, George W Booz, Raffaele Altara, et al.
Journal of Cardiac Failure
|
February 4, 2012
Survival benefit of implantable cardioverter-defibrillators in left ventricular assist device-supported heart failure patients
Marwan M Refaat, Toshikazu Tanaka, Robert L Kormos, et al.
Pacing and Clinical Electrophysiology : PACE
|
July 15, 2015
The Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long QT Syndrome
Kristian L Poulsen, Mostafa Hotait, Kirstine Calloe, et al.
Critical Pathways in Cardiology
|
June 24, 2015
Obstructive Sleep Apnea and Atrial Fibrillation: Pathophysiology and Implications for Treatment
Abhishek Maan, Moussa Mansour, Elad Anter, et al.
Circulation Research
|
June 11, 2011
A novel ryanodine receptor mutation linked to sudden death increases sensitivity to cytosolic calcium
Albano C Meli, Marwan M Refaat, Miroslav Dura, et al.
Annals of Hematology
|
July 8, 2021
Digital thermography and vascular involvement in β-thalassemia intermedia
Farah Abdulhai, Miran A Jaffa, Joseph Elias, et al.
Circulation. Arrhythmia and Electrophysiology
|
February 21, 2013
Characterization and mechanisms of action of novel NaV1.5 channel mutations associated with Brugada syndrome
Kirstine Calloe, Marwan M Refaat, Soren Grubb, et al.
Page
of 13