Publications by authors named "Alessandra Ranaldi"

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Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene Mutation.
Francesco Santoro, Maria D'Apolito, Ilaria Ragnatela, Alessandra Ranaldi, Alessandra Margaglione

J Cardiovasc Electrophysiol· September 2025

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Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study.
Maria d'Apolito, Francesco Santoro, Alessandra Ranaldi, Sara Cannito, Rosa Santacroce

Int J Mol Sci· January 2025

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Investigation of a Large Kindred Reveals Cardiac Calsequestrin () as a Cause of Brugada Syndrome.
Maria d'Apolito, Francesco Santoro, Alessandra Ranaldi, Ilaria Ragnatela, Anna Laura Colia

Genes (Basel)· June 2024

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De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis.
Maria d'Apolito, Alessandra Ranaldi, Francesco Santoro, Sara Cannito, Matteo Gravina

Int J Mol Sci· February 2024

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