M
Michael Eldar
Researcher at Sheba Medical Center
Publications - 167
Citations - 7986
Michael Eldar is an academic researcher from Sheba Medical Center. The author has contributed to research in topics: Ventricular tachycardia & Tachycardia. The author has an hindex of 45, co-authored 167 publications receiving 7551 citations. Previous affiliations of Michael Eldar include University of California, San Francisco.
Papers
More filters
Journal ArticleDOI
Effectiveness of Cardiac Resynchronization Therapy by QRS Morphology in the Multicenter Automatic Defibrillator Implantation Trial–Cardiac Resynchronization Therapy (MADIT-CRT)
Wojciech Zareba,Helmut U. Klein,Iwona Cygankiewicz,W. Jackson Hall,Scott McNitt,Mary Beth Brown,David S. Cannom,James P. Daubert,Michael Eldar,Michael R. Gold,Jeffrey J. Goldberger,Ilan Goldenberg,Edgar Lichstein,Heinz F. Pitschner,Mayer Rashtian,Scott D. Solomon,Sami Viskin,Paul J. Wang,Arthur J. Moss +18 more
TL;DR: No clinical benefit was observed in patients with a non-LBBB QRS pattern (right bundle-branch block or intraventricular conduction disturbances), and heart failure patients with New York Heart Association class I or II and LBBB derive substantial clinical benefit from CRT-D: a Reduction in heart failure progression and a reduction in the risk of ventricular tachyarrhythmias.
Journal ArticleDOI
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.
Hadas Lahat,Elon Pras,Tsviya Olender,Nili Avidan,Edna Ben-Asher,Orna Man,Etgar Levy-Nissenbaum,Asad Khoury,Avraham Lorber,Boleslaw Goldman,Doron Lancet,Michael Eldar +11 more
TL;DR: A missense mutation in a highly conserved region of the calsequestrin 2 gene (CASQ2) is described as the potential cause of the autosomal recessive form ofatecholamine-induced polymorphic ventricular tachycardia.
Journal ArticleDOI
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.
Michael Eldar,E. Pras,H. Lahat +2 more
TL;DR: A missense mutation in a highly conserved region of the calsequestrin 2 gene (CASQ2) is described as the potential cause of the autosomal recessive form ofatecholamine-induced polymorphic ventricular tachycardia.
Journal ArticleDOI
Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia Clinical Features and Assignment of the Disease Gene to Chromosome 1p13-21
Hadas Lahat,Michael Eldar,Etgar Levy-Nissenbaum,Tangiz Bahan,Eitan Friedman,Asad Khoury,Avraham Lorber,Daniel L. Kastner,Boleslaw Goldman,Elon Pras +9 more
TL;DR: This unique form of autosomal recessive PVT affects young children and may be lethal if left untreated and mapped the disease gene to chromosome 1p13-21.
Journal ArticleDOI
Long-term prognostic significance of left atrial volume in acute myocardial infarction.
Roy Beinart,Valentina Boyko,Ehud Schwammenthal,Rafael Kuperstein,Alex Sagie,Hanoch Hod,S Matetzky,Solomon Behar,Michael Eldar,Micha S. Feinberg +9 more
TL;DR: In patients with acute MI, increased LA volume, determined within the first 48 h of admission, is an independent predictor of five-year mortality with incremental prognostic information to clinical and echocardiographic data.