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Ilaria Ragnatela

Showing results (1-10 of 16) with videos related to

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Genes|February 25, 2023
A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico AnalysisMaria d'Apolito, Francesco Santoro, Rosa Santacroce, et al.
Heart Failure Reviews|December 2, 2023
Multidisciplinary approach in cardiomyopathies: From genetics to advanced imagingFrancesco Santoro, Enrica Vitale, Ilaria Ragnatela, et al.
International Journal of Molecular Sciences|February 13, 2025
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing StudyMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
International Journal of Molecular Sciences|March 13, 2024
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico AnalysisMaria d'Apolito, Alessandra Ranaldi, Francesco Santoro, et al.
Genes|July 27, 2024
Investigation of a Large Kindred Reveals Cardiac Calsequestrin (<i>CASQ2</i>) as a Cause of Brugada SyndromeMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
The American Journal of Cardiology|August 26, 2024
Impact of Frailty on Outcome of Older Patients With Non-ST Elevation Acute Myocardial Infarction Who Undergo Percutaneous Coronary InterventionMarco Mele, Ilaria Ragnatela, Matteo Romano, et al.
NPJ Cardiovascular Health|March 3, 2026
Psychological profile of patients with Brugada syndrome and the impact of its diagnosis and managementFrancesco Santoro, Luigi Di Biase, Antonio Curcio, et al.
Journal of Cardiovascular Electrophysiology|June 23, 2025
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene MutationFrancesco Santoro, Maria D'Apolito, Ilaria Ragnatela, et al.
Heart (British Cardiac Society)|September 4, 2023
Beta-blockers and renin-angiotensin system inhibitors for Takotsubo syndrome recurrence: a network meta-analysisFrancesco Santoro, Scott Sharkey, Rodolfo Citro, et al.
Atherosclerosis|November 13, 2025
Blood Cell Subtype patterns in Takotsubo Syndrome and acute coronary syndrome: analysis from the GEIST registryGiuseppina Novo, Luca Arcari, Cristina Madaudo, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Genes|February 25, 2023
A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico AnalysisMaria d'Apolito, Francesco Santoro, Rosa Santacroce, et al.
Heart Failure Reviews|December 2, 2023
Multidisciplinary approach in cardiomyopathies: From genetics to advanced imagingFrancesco Santoro, Enrica Vitale, Ilaria Ragnatela, et al.
International Journal of Molecular Sciences|February 13, 2025
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing StudyMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
International Journal of Molecular Sciences|March 13, 2024
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico AnalysisMaria d'Apolito, Alessandra Ranaldi, Francesco Santoro, et al.
Genes|July 27, 2024
Investigation of a Large Kindred Reveals Cardiac Calsequestrin (<i>CASQ2</i>) as a Cause of Brugada SyndromeMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
The American Journal of Cardiology|August 26, 2024
Impact of Frailty on Outcome of Older Patients With Non-ST Elevation Acute Myocardial Infarction Who Undergo Percutaneous Coronary InterventionMarco Mele, Ilaria Ragnatela, Matteo Romano, et al.
NPJ Cardiovascular Health|March 3, 2026
Psychological profile of patients with Brugada syndrome and the impact of its diagnosis and managementFrancesco Santoro, Luigi Di Biase, Antonio Curcio, et al.
Journal of Cardiovascular Electrophysiology|June 23, 2025
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene MutationFrancesco Santoro, Maria D'Apolito, Ilaria Ragnatela, et al.
Heart (British Cardiac Society)|September 4, 2023
Beta-blockers and renin-angiotensin system inhibitors for Takotsubo syndrome recurrence: a network meta-analysisFrancesco Santoro, Scott Sharkey, Rodolfo Citro, et al.
Atherosclerosis|November 13, 2025
Blood Cell Subtype patterns in Takotsubo Syndrome and acute coronary syndrome: analysis from the GEIST registryGiuseppina Novo, Luca Arcari, Cristina Madaudo, et al.
Pageof 2