Cardiopatías Familiares e xenética cardiovascular
Tel Aviv University
Tel Aviv, IsraelPublications in collaboration with researchers from Tel Aviv University (16)
2024
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Dosing and Safety Profile of Aficamten in Symptomatic Obstructive Hypertrophic Cardiomyopathy: Results From SEQUOIA-HCM
Journal of the American Heart Association, Vol. 13, Núm. 15, pp. e035993
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Impact of Aficamten on Disease and Symptom Burden in Obstructive Hypertrophic Cardiomyopathy: Results From SEQUOIA-HCM
Journal of the American College of Cardiology, Vol. 84, Núm. 19, pp. 1821-1831
2023
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Ventricular arrhythmias in patients with hypertrophic cardiomyopathy: Prevalence, distribution, predictors, and outcome
Heart Rhythm, Vol. 20, Núm. 10, pp. 1385-1392
2022
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Hypokinetic hypertrophic cardiomyopathy: clinical phenotype, genetics, and prognosis
ESC Heart Failure, Vol. 9, Núm. 4, pp. 2301-2312
2020
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Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European Registry
Circulation: Genomic and Precision Medicine, Vol. 13, Núm. 6, pp. E003117
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Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Journal of the American College of Cardiology, Vol. 75, Núm. 15, pp. 1772-1784
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Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews
International Journal of Cardiology, Vol. 317, pp. 133-138
2019
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Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Journal of Cellular and Molecular Medicine, Vol. 23, Núm. 3, pp. 2125-2135
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The impact of diabetes mellitus on the clinical phenotype of hypertrophic cardiomyopathy
European Heart Journal, Vol. 40, Núm. 21, pp. 1671-1677
2018
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European expert consensus statement on therapeutic goals in Fabry disease
Molecular Genetics and Metabolism, Vol. 124, Núm. 3, pp. 189-203
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Modeling peripartum cardiomyopathy with human induced pluripotent stem cells reveals distinctive abnormal function of cardiomyocytes
Circulation
2016
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Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
Journal of the American College of Cardiology, Vol. 68, Núm. 22, pp. 2440-2451
2015
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Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain
Heart, Vol. 101, Núm. 13, pp. 1047-1053
2014
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Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic
Israel Medical Association Journal, Vol. 16, Núm. 11, pp. 707
2012
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A family with recurrent sudden death and no clinical clue
Annals of Noninvasive Electrocardiology, Vol. 17, Núm. 4, pp. 387-393