Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Haitham, Hreibe"'
Autor:
Khalil, Jalkh, Kayla, Shahbazian, Phong, Nguyen, Wael, AlJaroudi, Evan, Hiner, Adnan, AlJaroudi, Haitham, Hreibe
Publikováno v:
In Journal of Electrocardiology July-August 2024 85:96-108
Publikováno v:
Case Reports in Cardiology, Vol 2023 (2023)
Leadless pacing systems have revolutionized the field of electrophysiology given its low complication rates and almost non-existent rate of infections compared with traditional pacemakers. These devices boast resistance to infections given its unique
Externí odkaz:
https://doaj.org/article/c3a68ab54a4648d992937c1beb29a420
Autor:
N. Stanley Nahman, Taylor Payne, Jennifer L. Waller, Joyce Maalouf, Haitham Hreibe, Mufaddal Kheda, Aaron Gopal
Publikováno v:
The Journal of Innovations in Cardiac Rhythm Management
End-stage renal disease (ESRD) constitutes a major burden on the health-care system in the United States, with more than 300,000 patients nationwide being treated with renal replacement therapy. Very few studies to date have evaluated the benefit of
Publikováno v:
AA practice. 14(11)
Autor:
Abdullah Omar, Haitham Hreibe, Adam E. Berman, Joyce Maalouf, Hoyle Whiteside, Ajay Pillai, Samir Saba
Publikováno v:
Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing. 59(3)
Pulmonary vein isolation (PVI) with cryoballoon ablation (CBA) is routinely guided by fluoroscopy and utilizes contrast injection to ensure catheter positioning and pulmonary vein occlusion. Non-fluoroscopic imaging techniques including electromagnet
Publikováno v:
Journal of the American College of Cardiology. 73:461
Pulmonary vein isolation (PVI) with cryoballoon ablation (CBA) is routinely guided by fluoroscopy and utilizes contrast to ensure catheter positioning. Non-fluoroscopic techniques include electromagnetic mapping (EM) and intracardiac echocardiography
CONGENITAL LONG QT SYNDROME TYPE 2: THE CASE OF A MISDIAGNOSED ARRHYTHMIA AND A NEAR FALL FROM DEATH
Publikováno v:
Journal of the American College of Cardiology. 73:2929
Long QT Syndrome-2 (LQT2) is a rare congenital disorder of ventricular myocardial repolarization due to heterozygous mutations in the alpha subunit of the rapid rectifier potassium channel of HERG and MiRP1 genes resulting in slowing of cardiac potas
Publikováno v:
Journal of the American College of Cardiology. 71:A2589