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International Journal of Cardiology|December 10, 2013
Titin mutation in familial restrictive cardiomyopathyYael Peled, Michael Gramlich, Guy Yoskovitz, et al.Circulation|November 9, 2005
Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathyFerhaan Ahmad, Michael Arad, Nicolas Musi, et al.Elife|June 28, 2022
<i>SNTA1</i> gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patientsEric N Jimenez-Vazquez, Michael Arad, Álvaro Macías, et al.Journal of the American College of Cardiology|October 11, 2023
International Consensus on Differential Diagnosis and Management of Patients With Danon Disease: JACC State-of-the-Art ReviewKimberly N Hong, Emily A Eshraghian, Michael Arad, et al.Journal of the American Heart Association|March 12, 2024
Sustained Pericarditis Recurrence Risk Reduction With Long-Term RilonaceptMassimo Imazio, Allan L Klein, Antonio Brucato, et al.Heart (British Cardiac Society)|May 4, 2015
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chainDiego García-Giustiniani, Michael Arad, Martín Ortíz-Genga, et al.Circulation. Genomic and Precision Medicine|November 10, 2025
Mavacamten Monotherapy in Real-World Patients with Obstructive Hypertrophic Cardiomyopathy: Evidence From COLLIGO-HCMOzlem Bilen, Arnon Shmuel Adler, Rachel Bastiaenen, et al.Circulation. Genomic and Precision Medicine|November 5, 2020
Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European RegistryDor Lotan, Joel Salazar-Mendiguchía, Jens Mogensen, et al.Plos One|October 18, 2018
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathyRevital Schick, Lucy N Mekies, Yuval Shemer, et al.European Journal of Neurology|January 29, 2025
Hereditary Transthyretin Amyloidosis in Israel: Genetic Landscape and Clinical CharacteristicsAmir Dori, Odelia Chorin, Noa Ruhrman-Shahar, et al.Pageof 15