Canlyniadau Chwilio - Avraham Lorber
- Dangos 1 - 9 canlyniadau o 9
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Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia gan Hadas Lahat, Michael Eldar, Etgar Levy‐Nissenbaum, Tangiz Bahan, Eitan Friedman, Asad Khoury, Avraham Lorber, Daniel L. Kastner, Boleslaw Goldman, Elon Pras
Cyhoeddwyd 2001Artigo -
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Functional abnormalities in iPSC‐derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations gan Atara Novak, Lili Barad, Avraham Lorber, Mihaela Gherghiceanu, Irina Reiter, Binyamin Eisen, Liron Eldor, Joseph Itskovitz‐Eldor, Michael Eldar, Michael Arad, Ofer Binah
Cyhoeddwyd 2015Artigo -
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Human Embryonic and Induced Pluripotent Stem Cell–Derived Cardiomyocytes Exhibit Beat Rate Variability and Power-Law Behavior gan Yael Mandel, Amir Weissman, Revital Schick, Lili Barad, Atara Novak, Gideon Meiry, Stanislav Goldberg, Avraham Lorber, Michael R. Rosen, Joseph Itskovitz‐Eldor, Ofer Binah
Cyhoeddwyd 2012Artigo -
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A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from... gan 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
Cyhoeddwyd 2001Artigo -
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A current and future outlook on upcoming technologies in remote monitoring of patients with heart failure gan Tarek Bekfani, Marat Fudim, John G.F. Cleland, Ana Jorbenadze, Stephan von Haehling, Avraham Lorber, Alexander Rothman, Kenneth M. Steín, William T. Abraham, Horst Sievert, Stefan D. Anker
Cyhoeddwyd 2020Revisão -
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Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype gan Adel Shalata, Ann Saada, Mohammed Mahroum, Yarin Hadid, Chaya Furman, Zaher Eldin Shalata, Robert J. Desnick, Avraham Lorber, Asaad Khoury, Adnan Higazi, Avraham Shaag, V. Barash, Ronen Spiegel, Euvgeni Vlodavsky, Pierre Rustin, Shmuel Pietrokovski, Irena Manov, Dan Gieger, Galit Tal, Adi Salzberg, Hanna Mandel
Cyhoeddwyd 2025Revisão -
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Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation gan Dirk J. Lefeber, Arjan P.M. de Brouwer, Éva Morava, Moniek Riemersma, Janneke Schuurs-Hoeijmakers, Birgit Absmanner, Kiek Verrijp, Willem M.R. van den Akker, Karin Huijben, Gerry Steenbergen, Jeroen van Reeuwijk, Adam Jóźwiak, Nili Zucker, Avraham Lorber, Martin Lammens, Carlos Knopf, Hans van Bokhoven, Stephanie Grünewald, Ludwig Lehle, Livia Kapusta, Hanna Mandel, Ron A. Wevers
Cyhoeddwyd 2011Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Medicine
Biology
Internal medicine
Cardiology
Gene
Genetics
Blood pressure
Catecholaminergic polymorphic ventricular tachycardia
Ryanodine receptor
Ryanodine receptor 2
Cell biology
Endocrinology
Heart failure
Heart rate
Locus (genetics)
Mutation
Phenotype
Receptor
Acoustics
Adrenergic
Asymptomatic
Atrial fibrillation
Beat (acoustics)
Biochemistry
Biosynthesis
Bradycardia
Caffeine
Calcium
Calsequestrin
Cardiac arrhythmia