Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Antonietta Buonaiuto"'
Autor:
Marco Ferrone, Michele Ciccarelli, Fahimeh Varzideh, Urna Kansakar, Germano Guerra, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Antonella Fiordelisi, Enzo Venga, Mafalda Esposito, Antonio Rainone, Roberto Ricciardi, Carmine Del Giudice, Fabio Minicucci, Tullio Tesorio, Valeria Visco, Guido Iaccarino, Jessica Gambardella, Gaetano Santulli, Pasquale Mone
Publikováno v:
Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-7 (2024)
Abstract Ischemia with non-obstructive coronary artery (INOCA) is a common cause of hospital admissions, leading to negative outcomes and reduced quality of life. Central to its pathophysiology is endothelial dysfunction, which contributes to myocard
Externí odkaz:
https://doaj.org/article/f10488e065b544179cec1e5ac7303bcd
Autor:
Oriana De Marco, Jessica Gambardella, Antonio Bianco, Antonella Fiordelisi, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Roberta Avvisato, Ivana Capuano, Maria Amicone, Teodolinda Di Risi, Eleonora Riccio, Letizia Spinelli, Antonio Pisani, Guido Iaccarino, Daniela Sorriento
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Fabry disease (FD), also known as Anderson-Fabry disease, is a hereditary disorder of glycosphingolipid metabolism, caused by a deficiency of the lysosomal alpha-galactosidase A enzyme. This causes a progressive accumulation of glycosphingolipids in
Externí odkaz:
https://doaj.org/article/c946a08cf9ab4942b405442ef45de95c
Autor:
Jessica Gambardella, Eleonora Riccio, Antonio Bianco, Antonella Fiordelisi, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Teodolinda Di Risi, Alessandro Viti, Roberta Avvisato, Antonio Pisani, Daniela Sorriento, Guido Iaccarino
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Fabry disease (FD) is a lysosomal storage disorder due to the impaired activity of the α-galactosidase A (GLA) enzyme which induces Gb3 deposition and multiorgan dysfunction. Exercise intolerance and fatigue are frequent and early findings in FD pat
Externí odkaz:
https://doaj.org/article/50839b4c01d849d3a4dcfea61ff3738e
Autor:
Jessica Gambardella, Antonella Fiordelisi, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Roberta Avvisato, Alessandro Viti, Eduardo Sommella, Fabrizio Merciai, Emanuela Salviati, Pietro Campiglia, Valeria D’Argenio, Silvia Parisi, Antonio Bianco, Letizia Spinelli, Eugenio Di Vaia, Alberto Cuocolo, Antonio Pisani, Eleonora Riccio, Teodolinda Di Risi, Michele Ciccarelli, Gaetano Santulli, Daniela Sorriento, Guido Iaccarino
Publikováno v:
iScience, Vol 26, Iss 3, Pp 106074- (2023)
Summary: Skeletal muscle (SM) pain and fatigue are common in Fabry disease (FD). Here, we undertook the investigation of the energetic mechanisms related to FD-SM phenotype. A reduced tolerance to aerobic activity and lactate accumulation occurred in
Externí odkaz:
https://doaj.org/article/d166a40b8e274a6c854f21c19acb1579
Autor:
Jessica Gambardella, Antonella Fiordelisi, Daniela Sorriento, Federica Cerasuolo, Antonietta Buonaiuto, Roberta Avvisato, Antonio Pisani, Fahimeh Varzideh, Eleonora Riccio, Gaetano Santulli, Guido Iaccarino
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 384:72-78
Fabry disease (FD) is a lysosomal storage disorder caused by mutations in the gene for alpha- galactosidase A (GAL) inducing a progressive accumulation of globotriaosylceramide (Gb3) and its metabolites in different organs and tissues. GB3 deposition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b57bf78c89cdde6bcda8d28e565ffc9c
https://doi.org/10.1124/jpet.122.001250
https://doi.org/10.1124/jpet.122.001250