Halloysite Nanotubes and Sepiolite for Health Applications

por Biddeci, Giuseppa, Spinelli, Gaetano, Colomba, Paolo, Di Blasi, Francesco
Publicado 2023

Nanomaterials: A Review about Halloysite Nanotubes, Properties, and Application in the Biological Field

por Biddeci, Giuseppa, Spinelli, Gaetano, Colomba, Paolo, Di Blasi, Francesco
Publicado 2022

A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report

por Pisani, Antonio, Imbriaco, Massimo, Zizzo, Carmela, Albeggiani, Giuseppe, Colomba, Paolo, Alessandro, Riccardo, Iemolo, Francesco, Duro, Giovanni
Publicado 2012

De novo mutation in a male patient with Fabry disease: a case report

por Iemolo, Francesco, Pizzo, Federica, Albeggiani, Giuseppe, Zizzo, Carmela, Colomba, Paolo, Scalia, Simone, Bartolotta, Caterina, Duro, Giovanni
Publicado 2014

Sex Differences in Anderson–Fabry Cardiomyopathy: Clinical, Genetic, and Imaging Analysis in Women

por Faro, Denise Cristiana, Losi, Valentina, Rodolico, Margherita Stefania, Torrisi, Elvira Mariateresa, Colomba, Paolo, Duro, Giovanni, Monte, Ines Paola
Publicado 2023

Hemochromatosis Mimicked Gaucher Disease: Role of Hyperferritinemia in Evaluation of a Clinical Case

por Zizzo, Carmela, Ruggeri, Irene, Colomba, Paolo, Argano, Christiano, Francofonte, Daniele, Zora, Marcomaria, Marsana, Emanuela Maria, Duro, Giovanni, Corrao, Salvatore
Publicado 2022

A pilot study of circulating microRNAs as potential biomarkers of Fabry disease

por Cammarata, Giuseppe, Scalia, Simone, Colomba, Paolo, Zizzo, Carmela, Pisani, Antonio, Riccio, Eleonora, Montalbano, Michaela, Alessandro, Riccardo, Giordano, Antonello, Duro, Giovanni
Publicado 2018

Late-Onset Pompe Disease with Normal Creatine Kinase Levels: The Importance of Rheumatological Suspicion

por Marotto, Daniela, Moschetti, Marta, Lo Curto, Alessia, Spezzigu, Anna M., Giacomarra, Miriam, Marsana, Emanuela M., Zizzo, Carmela, Duro, Giovanni, Colomba, Paolo
Publicado 2023

Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs

por Colomba, Paolo, Zizzo, Carmela, Alessandro, Riccardo, Cammarata, Giuseppe, Scalia, Simone, Giordano, Antonello, Pieroni, Maurizio, Sicurella, Luigi, Amico, Luisa, Burlina, Alessandro, Duro, Giovanni
Publicado 2018

High Variability of Fabry Disease Manifestations in an Extended Italian Family

por Cammarata, Giuseppe, Fatuzzo, Pasquale, Rodolico, Margherita Stefania, Colomba, Paolo, Sicurella, Luigi, Iemolo, Francesco, Zizzo, Carmela, Alessandro, Riccardo, Bartolotta, Caterina, Duro, Giovanni, Monte, Ines
Publicado 2015

Identification of Biomarkers in Cerebrospinal Fluid and Serum of Multiple Sclerosis Patients by Immunoproteomics Approach

por Colomba, Paolo, Fontana, Simona, Salemi, Giuseppe, Barranca, Marilisa, Lo Sicco, Claudia, Mazzola, Maria Antonietta, Ragonese, Paolo, Savettieri, Giovanni, De Leo, Giacomo, Alessandro, Riccardo, Duro, Giovanni
Publicado 2014

Diagnosing Fabry nephropathy: the challenge of multiple kidney disease

por Esposito, Pasquale, Caputo, Carmela, Repetto, Monica, Somaschini, Alberto, Pietro, Bellone, Colomba, Paolo, Zizzo, Carmela, Parodi, Angelica, Zanetti, Valentina, Canepa, Marco, Eustachi, Virginia, Sanguineri, Francesca, Mandich, Paola, Viazzi, Francesca
Publicado 2023

Pompe disease: pathogenesis, molecular genetics and diagnosis

por Taverna, Simona, Cammarata, Giuseppe, Colomba, Paolo, Sciarrino, Serafina, Zizzo, Carmela, Francofonte, Daniele, Zora, Marco, Scalia, Simone, Brando, Chiara, Curto, Alessia Lo, Marsana, Emanuela Maria, Olivieri, Roberta, Vitale, Silvia, Duro, Giovanni
Publicado 2020

Inter-familial and intra-familial phenotypic variability in three Sicilian families with Anderson-Fabry disease

por Tuttolomondo, Antonino, Simonetta, Irene, Duro, Giovanni, Pecoraro, Rosaria, Miceli, Salvatore, Colomba, Paolo, Zizzo, Carmela, Nucera, Antonia, Daidone, Mario, Di Chiara, Tiziana, Scaglione, Rosario, Della Corte, Vittoriano, Corpora, Francesca, Vogiatzis, Danai, Pinto, Antonio
Publicado 2017

Can Be miR-126-3p a Biomarker of Premature Aging? An Ex Vivo and In Vitro Study in Fabry Disease

por Lo Curto, Alessia, Taverna, Simona, Costa, Maria Assunta, Passantino, Rosa, Augello, Giuseppa, Adamo, Giorgia, Aiello, Anna, Colomba, Paolo, Zizzo, Carmela, Zora, Marco, Accardi, Giulia, Candore, Giuseppina, Francofonte, Daniele, Di Chiara, Tiziana, Alessandro, Riccardo, Caruso, Calogero, Duro, Giovanni, Cammarata, Giuseppe
Publicado 2021

miR-126-3p and miR-21-5p as Hallmarks of Bio-Positive Ageing; Correlation Analysis and Machine Learning Prediction in Young to Ultra-Centenarian Sicilian Population

por Accardi, Giulia, Bono, Filippa, Cammarata, Giuseppe, Aiello, Anna, Herrero, Maria Trinidad, Alessandro, Riccardo, Augello, Giuseppa, Carru, Ciriaco, Colomba, Paolo, Costa, Maria Assunta, De Vivo, Immaculata, Ligotti, Mattia Emanuela, Lo Curto, Alessia, Passantino, Rosa, Taverna, Simona, Zizzo, Carmela, Duro, Giovanni, Caruso, Calogero, Candore, Giuseppina
Publicado 2022

Mutations in the GLA Gene and LysoGb3: Is It Really Anderson-Fabry Disease?

por Duro, Giovanni, Zizzo, Carmela, Cammarata, Giuseppe, Burlina, Alessandro, Burlina, Alberto, Polo, Giulia, Scalia, Simone, Oliveri, Roberta, Sciarrino, Serafina, Francofonte, Daniele, Alessandro, Riccardo, Pisani, Antonio, Palladino, Giuseppe, Napoletano, Rosa, Tenuta, Maurizio, Masarone, Daniele, Limongelli, Giuseppe, Riccio, Eleonora, Frustaci, Andrea, Chimenti, Cristina, Ferri, Claudio, Pieruzzi, Federico, Pieroni, Maurizio, Spada, Marco, Castana, Cinzia, Caserta, Marina, Monte, Ines, Rodolico, Margherita Stefania, Feriozzi, Sandro, Battaglia, Yuri, Amico, Luisa, Losi, Maria Angela, Autore, Camillo, Lombardi, Marco, Zoccali, Carmine, Testa, Alessandra, Postorino, Maurizio, Mignani, Renzo, Zachara, Elisabetta, Giordano, Antonello, Colomba, Paolo
Publicado 2018