Molecular genetics made simple

por Kassem, Heba Sh., Girolami, Francesca, Sanoudou, Despina
Publicado 2012

Genetic profile of hypertrophic cardiomyopathy in Tunisia: Is it different?

por Jaafar, Nawel, Girolami, Francesca, Zairi, Ihsen, Kraiem, Sondes, Hammami, Mohamed, Olivotto, Iacopo
Publicado 2015

Bioinformatics for Next Generation Sequencing Data

por Magi, Alberto, Benelli, Matteo, Gozzini, Alessia, Girolami, Francesca, Torricelli, Francesca, Brandi, Maria Luisa
Publicado 2010

Genetic advances in sarcomeric cardiomyopathies: state of the art

por Ho, Carolyn Y., Charron, Philippe, Richard, Pascale, Girolami, Francesca, Van Spaendonck-Zwarts, Karin Y., Pinto, Yigal
Publicado 2015

Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?

por Mazzarotto, Francesco, Olivotto, Iacopo, Boschi, Beatrice, Girolami, Francesca, Poggesi, Corrado, Barton, Paul J. R., Walsh, Roddy
Publicado 2020

Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome: Protecting Families

por De Gregorio, Maria Grazia, Girolami, Francesca, Tomberli, Benedetta, Rossi, Guendalina, Tomberli, Alessia, Baldini, Katia, Olivotto, Iacopo
Publicado 2020

Bicuspid Aortic Valve in Children and Adolescents: A Comprehensive Review

por Spaziani, Gaia, Girolami, Francesca, Arcieri, Luigi, Calabri, Giovanni Battista, Porcedda, Giulio, Di Filippo, Chiara, Surace, Francesca Chiara, Pozzi, Marco, Favilli, Silvia
Publicado 2022

Aortic Dilatation in Pediatric Patients with Bicuspid Aortic Valve: How the Choice of Nomograms May Change Prevalence

por Spaziani, Gaia, Bonanni, Francesca, Girolami, Francesca, Bennati, Elena, Calabri, Giovanni Battista, Di Filippo, Chiara, Porcedda, Giulio, Passantino, Silvia, Nistri, Stefano, Olivotto, Iacopo, Favilli, Silvia
Publicado 2023

Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

por Girolami, Francesca, Frisso, Giulia, Benelli, Matteo, Crotti, Lia, Iascone, Maria, Mango, Ruggiero, Mazzaccara, Cristina, Pilichou, Kalliope, Arbustini, Eloisa, Tomberli, Benedetta, Limongelli, Giuseppe, Basso, Cristina, Olivotto, Iacopo
Publicado 2018

Mitochondrial Energetics and Ca(2+)-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy

por Lombardi, Maria, Lazzeroni, Davide, Pisano, Annalinda, Girolami, Francesca, Alfieri, Ottavio, La Canna, Giovanni, d’Amati, Giulia, Olivotto, Iacopo, Rimoldi, Ornella E., Foglieni, Chiara, Camici, Paolo G.
Publicado 2020

A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis

por Spinelli, Valentina, Girolami, Francesca, Marrone, Chiara, Consigli, Veronica, Iascone, Maria, Passantino, Silvia, Porcedda, Giulio, Calabri, Giovanni Battista, De Simone, Luciano, Olivotto, Iacopo, Santoro, Giuseppe, Favilli, Silvia
Publicado 2020

Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry

por Girolami, Francesca, Spinelli, Valentina, Maurizi, Niccolò, Focardi, Martina, Nesi, Gabriella, Maio, Vincenza, Grifoni, Rossella, Albora, Giuseppe, Bertaccini, Bruno, Targetti, Mattia, Coppini, Raffaele, Favilli, Silvia, Olivotto, Iacopo, Cerbai, Elisabetta
Publicado 2022

Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

por Coppini, Raffaele, Ho, Carolyn Y., Ashley, Euan, Day, Sharlene, Ferrantini, Cecilia, Girolami, Francesca, Tomberli, Benedetta, Bardi, Sara, Torricelli, Francesca, Cecchi, Franco, Mugelli, Alessandro, Poggesi, Corrado, Tardiff, Jil, Olivotto, Iacopo
Publicado 2014

Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked Questions

por Girolami, Francesca, Gozzini, Alessia, Pálinkás, Eszter Dalma, Ballerini, Adelaide, Tomberli, Alessia, Baldini, Katia, Marchi, Alberto, Zampieri, Mattia, Passantino, Silvia, Porcedda, Giulio, Calabri, Giovanni Battista, Bennati, Elena, Spaziani, Gaia, Crotti, Lia, Cecchi, Franco, Favilli, Silvia, Olivotto, Iacopo
Publicado 2023

Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center

por Mazzarotto, Francesco, Girolami, Francesca, Boschi, Beatrice, Barlocco, Fausto, Tomberli, Alessia, Baldini, Katia, Coppini, Raffaele, Tanini, Ilaria, Bardi, Sara, Contini, Elisa, Cecchi, Franco, Pelo, Elisabetta, Cook, Stuart A., Cerbai, Elisabetta, Poggesi, Corrado, Torricelli, Francesca, Walsh, Roddy, Olivotto, Iacopo
Publicado 2018

Myosins and MyomiR Network in Patients with Obstructive Hypertrophic Cardiomyopathy

por Foglieni, Chiara, Lombardi, Maria, Lazzeroni, Davide, Zerboni, Riccardo, Lazzarini, Edoardo, Bertoli, Gloria, Pisano, Annalinda, Girolami, Francesca, Andolfo, Annapaola, Magagnotti, Cinzia, Peretto, Giovanni, Sartorio, Carmem L., Olivotto, Iacopo, La Canna, Giovanni, Alfieri, Ottavio, Rimoldi, Ornella E., Barile, Lucio, d’Amati, Giulia, Camici, Paolo G.
Publicado 2022

Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)

por Ho, Carolyn Y., Day, Sharlene M., Ashley, Euan A., Michels, Michelle, Pereira, Alexandre C., Jacoby, Daniel, Cirino, Allison L., Fox, Jonathan C., Lakdawala, Neal K., Ware, James S., Caleshu, Colleen A., Helms, Adam S., Colan, Steven D., Girolami, Francesca, Cecchi, Franco, Seidman, Christine E., Sajeev, Gautam, Signorovitch, James, Green, Eric M., Olivotto, Iacopo
Publicado 2018

Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human MYBPC3 HCM

por Pioner, Josè Manuel, Vitale, Giulia, Steczina, Sonette, Langione, Marianna, Margara, Francesca, Santini, Lorenzo, Giardini, Francesco, Lazzeri, Erica, Piroddi, Nicoletta, Scellini, Beatrice, Palandri, Chiara, Schuldt, Maike, Spinelli, Valentina, Girolami, Francesca, Mazzarotto, Francesco, van der Velden, Jolanda, Cerbai, Elisabetta, Tesi, Chiara, Olivotto, Iacopo, Bueno-Orovio, Alfonso, Sacconi, Leonardo, Coppini, Raffaele, Ferrantini, Cecilia, Regnier, Michael, Poggesi, Corrado
Publicado 2023

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

por Mazzarotto, Francesco, Hawley, Megan H., Beltrami, Matteo, Beekman, Leander, de Marvao, Antonio, McGurk, Kathryn A., Statton, Ben, Boschi, Beatrice, Girolami, Francesca, Roberts, Angharad M., Lodder, Elisabeth M., Allouba, Mona, Romeih, Soha, Aguib, Yasmine, Baksi, A. John, Pantazis, Antonis, Prasad, Sanjay K., Cerbai, Elisabetta, Yacoub, Magdi H., O’Regan, Declan P., Cook, Stuart A., Ware, James S., Funke, Birgit, Olivotto, Iacopo, Bezzina, Connie R., Barton, Paul J. R., Walsh, Roddy
Publicado 2021

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

por Crotti, Lia, Spazzolini, Carla, Nyegaard, Mette, Overgaard, Michael T, Kotta, Maria-Christina, Dagradi, Federica, Sala, Luca, Aiba, Takeshi, Ayers, Mark D, Baban, Anwar, Barc, Julien, Beach, Cheyenne M, Behr, Elijah R, Bos, J Martijn, Cerrone, Marina, Covi, Peter, Cuneo, Bettina, Denjoy, Isabelle, Donner, Birgit, Elbert, Adrienne, Eliasson, Håkan, Etheridge, Susan P, Fukuyama, Megumi, Girolami, Francesca, Hamilton, Robert, Horie, Minoru, Iascone, Maria, Jaimez, Juan Jiménez, Jensen, Henrik Kjærulf, Kannankeril, Prince J, Kaski, Juan P, Makita, Naomasa, Muñoz-Esparza, Carmen, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Porretta, Alessandra Pia, Prandstetter, Christopher, Probst, Vincent, Robyns, Tomas, Rosenthal, Eric, Rosés-Noguer, Ferran, Sekarski, Nicole, Singh, Anoop, Spentzou, Georgia, Stute, Fridrike, Tfelt-Hansen, Jacob, Till, Jan, Tobert, Kathryn E, Vinocur, Jeffrey M, Webster, Gregory, Wilde, Arthur A M, Wolf, Cordula M, Ackerman, Michael J, Schwartz, Peter J
Publicado 2023