Zobrazeno 1 - 10
of 167
pro vyhledávání: '"Avraham, Lorber"'
Autor:
Nili Schamroth Pravda, Ofra Kalter‐Leibovici, Amiram Nir, Avraham Lorber, Alexander Dadashev, Rafael Hirsch, Michal Benderly
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 9 (2024)
Background A significant percentage of patients with congenital heart disease surviving into adulthood will develop arrhythmias. These arrhythmias are associated with an increased risk of adverse events and death. We aimed to assess arrhythmia preval
Externí odkaz:
https://doaj.org/article/804e614cf1ce48dea1d9441ef8771c7f
Autor:
Miry Blich, Hodaya Oron, Wisam Darawsha, Mahmoud Suleiman, Lior Gepstein, Monther Boulos, Avraham Lorber, Asaad Kchoury
Publikováno v:
Journal of Arrhythmia, Vol 39, Iss 4, Pp 607-612 (2023)
Abstract Background Determining the pathogenesis of sudden cardiac arrest (SCA) in children is crucial for its management and prognosis. Our aim is to analyze the role of broad genetic testing in the prevention, diagnosis, and prognosis of SCA in Chi
Externí odkaz:
https://doaj.org/article/f2c0d73dcf8345caabccf8f0fa8d891a
Autor:
Sharon Brosilow, Wisam Abo Zaid, Daniel Maghen, Asaad Khoury, Doron Aharonson, Avraham Lorber
Publikováno v:
Cardiology in the Young. :1-4
Objectives: When cardiac muscle damage occurs, cardiac troponins are released to blood and their detection is used as a marker in clinical setting. The prognostic value of the quantitative levels of blood troponin I in cases of myocarditis and myoper
Autor:
Michal Benderly, Jonathan Buber, Ofra Kalter‐Leibovici, Leonard Blieden, Alexander Dadashev, Avraham Lorber, Amiram Nir, Sergei Yalonetsky, Gabriel Chodick, Dahlia Weitzman, Ran Balicer, Efrat Mazor Dray, Havi Murad, Yaron Razon, Rafael Hirsch
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 2 (2021)
Background Several studies have examined hospitalizations among patients with adult congenital heart disease (ACHD). Few investigated other services or utilization patterns. Our aim was to study service utilization patterns and predictors among patie
Externí odkaz:
https://doaj.org/article/b2ec3166e065495fb93880fd80b9ad1c
Autor:
Tzipora C Falik‐Zaccai, Yiftah Barsheshet, Hanna Mandel, Meital Segev, Avraham Lorber, Shachaf Gelberg, Limor Kalfon, Shani Ben Haroush, Adel Shalata, Liat Gelernter‐Yaniv, Sarah Chaim, Dorith Raviv Shay, Morad Khayat, Michal Werbner, Inbar Levi, Yishay Shoval, Galit Tal, Stavit Shalev, Eli Reuveni, Emily Avitan‐Hersh, Eugene Vlodavsky, Liat Appl‐Sarid, Dorit Goldsher, Reuven Bergman, Zvi Segal, Ora Bitterman‐Deutsch, Orly Avni
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 3, Pp 319-336 (2017)
Abstract Dilated cardiomyopathy (DCM) is a life‐threatening disorder whose genetic basis is heterogeneous and mostly unknown. Five Arab Christian infants, aged 4–30 months from four families, were diagnosed with DCM associated with mild skin, tee
Externí odkaz:
https://doaj.org/article/3bda5fe3b264454bbafad929188d4a0f
Publikováno v:
Cardiovascular Revascularization Medicine.
Autor:
Ibrahim Marai, Avraham Lorber, Ariela Lowenstein, Lee Greenblatt-Kimron, Galit Pinto, Miri Cohen
Publikováno v:
Experimental Aging Research. 48:136-149
Background Heart rate variability (HRV) has been suggested as an indicator of capacity to adapt effectively to physiological or environmental challenges and of physical and psychological health in old age. Aims The study assessed levels of high-frequ
Publikováno v:
International Heart Journal. 60:979-982
Congenital long QT syndrome (LQTS) is a cardiac channelopathy that leads to the prolongation of the QT interval. This prolongation can lead to ventricular tachyarrhythmia, syncope, and sudden cardiac death. There are various types of LQTS. Treatment
Autor:
Leonard C Blieden, Avraham Lorber, Amiram Nir, Dahlia Weitzman, Alexander Dadashev, Ofra Kalter-Leibovici, Sergei Yalonetsky, Michal Benderly, Jonathan Buber, Rafael Hirsch, Gabriel Chodick, Yaron Razon, Efrat Mazor-Dray
Publikováno v:
International Journal of Cardiology. 276:81-86
Background The significance of depression/anxiety among ACHD patients in terms of health care utilization is unknown and data on the association with mortality are scarce. Methods Analyses comprised 8334 ACHD patients, age ≥ 18 years, insured by a
Autor:
Amiram Nir, Yaron Razon, Gabriel Chodick, Havi Murad, Alexander Dadashev, Avraham Lorber, Rafael Hirsch, Ofra Kalter-Leibovici, Sergei Yalonetsky, Michal Benderly, Ran D. Balicer, Dahlia Weitzman, Jonathan Buber, Leonard C. Blieden, Efrat Mazor Dray
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Several studies have examined hospitalizations among patients with adult congenital heart disease (ACHD). Few investigated other services or utilization patterns. Our aim was to study service utilization patterns and predictors among patie