F. Borrelli
13 Papers
F. Borrelli is an academic researcher. The author has contributed to research in topics: Hypertrophic cardiomyopathy & Medicine. The author has an hindex of 1, co-authored 6 publications.
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Papers
Sarcomeric versus Non-Sarcomeric HCM
F. Borrelli,Maria Angela Losi,Grazia Canciello,G. Todde,E. Perillo,Giulia Frisso,Giovanni Esposito,R. Lombardi +7 more
TL;DR: In this paper , the authors describe the differences in the phenotypic expression and clinical outcomes of Sarc+ and Sarc− HCM and briefly discuss the current knowledge about HCM caused by rare non-sarcomeric mutations.
Prediction of incident atrial fibrillation in hypertrophic cardiomyopathy.
Maria Angela Losi,Emanuele Monda,R. Lombardi,Michele Lioncino,Grazia Canciello,Marta Rubino,G. Todde,Martina Caiazza,F. Borrelli,Adelaide Fusco,Annapaola Cirillo,E. Perillo,Joseph Sepe,Daniela Pacella,Giovanni de Simone,Paolo Calabrò,Giovanni Esposito,Giuseppe Limongelli +17 more
TL;DR: LA diameter, a worldwide and simple echocardiographic measure, is capable alone to predict AF development in HCM patients, and is shown to be capable alone of identifying patients at high risk to develop AF.
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Mechano-energetic efficiency in patients with hypertrophic cardiomyopathy with and without sarcomeric mutations.
F. Borrelli,R. Lombardi,Grazia Canciello,Giulia Frisso,G. Todde,Giovanni Esposito,Maria Angela Losi +6 more
TL;DR: Lower MEEi in HCM with sarcomeric mutation is not related to significant differences on filling pressure as shown on P/V analysis, and may predict a positive genetic analysis.
1
Left atrial size trajectories and outcome over a 35-year follow-up in patients with hypertrophic cardiomyopathy.
Salvatore di Napoli,Daniela Pacella,L. Ordine,Grazia Canciello,F. Borrelli,Lorenzo Moscano,Raffaele Martorano,R. Polizzi,Brigida Napolitano,Alessandra Spinelli,R. Lombardi,Giovanni Esposito,Maria Angela Losi +12 more
1
Abstract 15004: Characterization of Hypertrophic Cardiomyopathy Caused by Mutations in Four and a Half Lim Domains 1 Gene
Maria Angela Losi,F. Borrelli,Chiara Calore,Grazia Canciello,Fiore Manganelli,Stefano Tozza,Luca Bello,Suet Nee Chen,Maria Bueno Marinas,Rudy Celeghin,Martina Perazzolo Marra,G. Todde,Giulia Frisso,Matthew D. Taylor,Kalliopi Pilichou,R. Lombardi +15 more
TL;DR: In this paper , the prevalence of mutations in the Four and Half Lim domain (FHL1), an X-chromosome gene, have been described in rare cases of Hypertrophic Cardiomyopathy (HCM), mainly associated with myopathy.