Fenestrated Atrial Septal Defect Percutaneously Occluded by a Single Device: Procedural and Financial Considerations

Por Tal, Roie, Dahud, Qarawani, Lorber, Avraham
Publicado em 2012

Transcatheter Amplatzer septal occluder closure of residual ASD shunt: following StarFlex spring protrusion

Por Khatib, Ihab, Schwartz, Yetzhak, Lorber, Avraham
Publicado no Heart Asia (2011)

Transcatheter closure of ruptured right-coronary aortic sinus fistula to right ventricle

Por Khoury, Asaad, Khatib, Ihab, Halabi, Majdi, Lorber, Avraham
Publicado em 2010

Modeling Catecholaminergic Polymorphic Ventricular Tachycardia using Induced Pluripotent Stem Cell-derived Cardiomyocytes

Por Novak, Atara, Barad, Lili, Lorber, Avraham, Itskovitz-Eldor, Joseph, Binah, Ofer
Publicado em 2012

Cardiac Function in Long-Term Survivors of Childhood Lymphoma

Por Friedberg, Mark K., Solt, Ido, Weyl-Ben-Arush, Myriam, Braver, Yulia, Lorber, Avraham
Publicado em 2011

Cardiomyocytes generated from CPVT(D307H) patients are arrhythmogenic in response to β-adrenergic stimulation

Por Novak, Atara, Barad, Lili, Zeevi-Levin, Naama, Shick, Revital, Shtrichman, Ronit, Lorber, Avraham, Itskovitz-Eldor, Joseph, Binah, Ofer
Publicado em 2012

Extreme clinical variability of dilated cardiomyopathy in two siblings with Alström syndrome

Por Mahamid, Jamal, Lorber, Avraham, Horovitz, Yoseph, Shalev, Stavit A, Collin, Gayle B, Naggert, Jürgen K, Marshall, Jan D, Spiegel, Ronen
Publicado em 2012

Functional abnormalities in iPSC-derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations

Por Novak, Atara, Barad, Lili, Lorber, Avraham, Gherghiceanu, Mihaela, Reiter, Irina, Eisen, Binyamin, Eldor, Liron, Itskovitz-Eldor, Joseph, Eldar, Michael, Arad, Michael, Binah, Ofer
Publicado no J Cell Mol Med (2015)

Human Embryonic and Induced Pluripotent Stem Cell–Derived Cardiomyocytes Exhibit Beat Rate Variability and Power-Law Behavior

Por Mandel, Yael, Weissman, Amir, Schick, Revital, Barad, Lili, Novak, Atara, Meiry, Gideon, Goldberg, Stanislav, Lorber, Avraham, Rosen, Michael R., Itskovitz-Eldor, Joseph, Binah, Ofer
Publicado em 2012

From beat rate variability in induced pluripotent stem cell-derived pacemaker cells to heart rate variability in human subjects

Por Ben-Ari, Meital, Schick, Revital, Barad, Lili, Novak, Atara, Ben-Ari, Erez, Lorber, Avraham, Itskovitz-Eldor, Joseph, Rosen, Michael R, Weissman, Amir, Binah, Ofer
Publicado no Heart Rhythm (2014)

A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from...

Por Lahat, Hadas, Pras, Elon, Olender, Tsviya, Avidan, Nili, Ben-Asher, Edna, Man, Orna, Levy-Nissenbaum, Etgar, Khoury, Asad, Lorber, Avraham, Goldman, Boleslaw, Lancet, Doron, Eldar, Michael
Publicado em 2001

From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG)

Por Kapusta, Livia, Zucker, Nili, Frenckel, George, Medalion, Benjamin, Gal, Tuvia Ben, Birk, Einat, Mandel, Hanna, Nasser, Nadim, Morgenstern, Sarah, Zuckermann, Andreas, Lefeber, Dirk J., de Brouwer, Arjen, Wevers, Ron A., Lorber, Avraham, Morava, Eva
Publicado em 2012

Investigating the cardiac pathology of SCO2‐mediated hypertrophic cardiomyopathy using patients induced pluripotent stem cell–derived cardiomyocytes

Por Hallas, Tova, Eisen, Binyamin, Shemer, Yuval, Ben Jehuda, Ronen, Mekies, Lucy N., Naor, Shulamit, Schick, Revital, Eliyahu, Sivan, Reiter, Irina, Vlodavsky, Eugene, Katz, Yeshayahu (Shai), Õunap, Katrin, Lorber, Avraham, Rodenburg, Richard, Mandel, Hanna, Gherghiceanu, Mihaela, Binah, Ofer
Publicado no J Cell Mol Med (2017)

Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation

Por Lefeber, Dirk J., de Brouwer, Arjan P. M., Morava, Eva, Riemersma, Moniek, Schuurs-Hoeijmakers, Janneke H. M., Absmanner, Birgit, Verrijp, Kiek, van den Akker, Willem M. R., Huijben, Karin, Steenbergen, Gerry, van Reeuwijk, Jeroen, Jozwiak, Adam, Zucker, Nili, Lorber, Avraham, Lammens, Martin, Knopf, Carlos, van Bokhoven, Hans, Grünewald, Stephanie, Lehle, Ludwig, Kapusta, Livia, Mandel, Hanna, Wevers, Ron A.
Publicado em 2011

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

Por Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly
Publicado no EMBO Mol Med (2017)

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

Por Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly
Publicado no EMBO Mol Med (2017)