Modeling Catecholaminergic Polymorphic Ventricular Tachycardia using Induced Pluripotent Stem Cell-derived Cardiomyocytes by Atara Novak, Avraham Lorber, Joseph Itskovitz-Eldor, Ofer Binah

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THE OCCURRENCE OF CHEYNE STOKES RESPIRATION IN CONGESTIVE HEART FAILURE: THE EFFECT OF AGE by Avivit Pe'Er, Avraham Lorber, Suheir Suraiya, Atul Malhotra, Giora Pillar

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Cardiac Function in Long-Term Survivors of Childhood Lymphoma by Mark K. Friedberg, Ido Solt, Myriam Weyl-Ben-Arush, Yulia Braver, Avraham Lorber

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Arrhythmia Burden Among Adult Patients With Congenital Heart Disease: A Population‐Based Study by Nili Schamroth Pravda, Ofra Kalter‐Leibovici, Amiram Nir, Avraham Lorber, Alexander Dadashev, Rafael Hirsch, Michal Benderly

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The role of genetic testing in the prevention, diagnosis, and prognosis of sudden cardiac arrest in children by Miry Blich, Hodaya Oron, Wisam Darawsha, Mahmoud Suleiman, Lior Gepstein, Monther Boulos, Avraham Lorber, Asaad Kchoury

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Health Service Utilization Patterns Among Adults With Congenital Heart Disease: A Population‐Based Study by 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

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Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype by Adel Shalata, Ann Saada, Mohammed Mahroum, Yarin Hadid, Chaya Furman, Zaher Eldin Shalata, Robert J. Desnick, Avraham Lorber, Asaad Khoury, Adnan Higazi, Avraham Shaag, Varda Barash, Ronen Spiegel, Euvgeni Vlodavsky, Pierre Rustin, Shmuel Pietrokovski, Irena Manov, Dan Gieger, Galit Tal, Adi Salzberg, Hanna Mandel

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Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. by Dirk J Lefeber, Arjan P M de Brouwer, Eva Morava, Moniek Riemersma, Janneke H M Schuurs-Hoeijmakers, Birgit Absmanner, Kiek Verrijp, Willem M R van den Akker, Karin Huijben, Gerry Steenbergen, Jeroen van Reeuwijk, Adam Jozwiak, Nili Zucker, Avraham Lorber, Martin Lammens, Carlos Knopf, Hans van Bokhoven, Stephanie Grünewald, Ludwig Lehle, Livia Kapusta, Hanna Mandel, Ron A Wevers

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome by 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

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome by 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

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