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International Journal of Cardiology|September 21, 2024
The "Padua classification" of cardiomyopathies: Combining pathobiological basis and morpho-functional remodelingDomenico Corrado, Gaetano Thiene, Barbara Bauce, et al.
Journal of Neurology|March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutationsPietro Riguzzi, Daniele Sabbatini, Aurora Fusto, et al.
European Journal of Human Genetics : EJHG|July 13, 2017
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathyMarzia De Bortoli, Chiara Calore, Alessandra Lorenzon, et al.
International Journal of Cardiology|January 15, 2022
Strength of clinical indication and therapeutic impact of the implantable cardioverter defibrillator in patients with hypertrophic cardiomyopathyCarlo Fumagalli, Valentina De Filippo, Chiara Zocchi, et al.
Neurology|September 28, 2018
The clinical spectrum of CASQ1-related myopathyClaudio Semplicini, Cinzia Bertolin, Luca Bello, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|February 21, 2025
The 'Padua classification' of cardiomyopathies into three groups: hypertrophic/restrictive, dilated/hypokinetic, and scarring/arrhythmogenicDomenico Corrado, Francesca Graziano, Barbara Bauce, et al.
Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.
International Journal of Cardiology|January 19, 2024
Clinical characteristics and outcome of end stage hypertrophic cardiomyopathy: Role of age and heart failure phenotypesBeatrice Musumeci, Giacomo Tini, Elena Biagini, et al.
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