Zobrazeno 1 - 10
of 648
pro vyhledávání: '"A. Sorriento"'
Autor:
A. Sorriento, A. Cafarelli, P. Spinnato, A. Russo, G. Lisignoli, F. Rabusseau, P. Cabras, E. Dumont, L. Ricotti
Publikováno v:
IEEE Journal of Translational Engineering in Health and Medicine, Vol 10, Pp 1-8 (2022)
Objective: A repeatable and reliable follow-up of knee injuries would be desirable to prevent delayed diagnosis and to monitor the efficacy of the applied treatment over time. Ultrasound (US) techniques are an attractive option to this purpose, since
Externí odkaz:
https://doaj.org/article/ab53eace4b13466e936a93e0766a6cd6
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Bone fracture is a continuous process, during which bone mineral matrix evolves leading to an increase in hydroxyapatite and calcium carbonate content. Currently, no gold standard methods are available for a quantitative assessment of bone f
Externí odkaz:
https://doaj.org/article/c14fd3a72eb14c79a73bef384b23d6e6
Autor:
Andrea Cafarelli, Angela Sorriento, Giorgia Marola, Denise Amram, Fabien Rabusseau, Herve Locteau, Paolo Cabras, Erik Dumont, Sam Nakhaei, Ake Jernberger, Par Bergsten, Paolo Spinnato, Alessandro Russo, Leonardo Ricotti
Publikováno v:
IEEE Open Journal of Engineering in Medicine and Biology, Vol 5, Pp 476-484 (2024)
Goal: To evaluate the usability of different technologies designed for a remote assessment of knee osteoarthritis. Methods: We recruited eleven patients affected by mild or moderate knee osteoarthritis, eleven caregivers, and eleven clinicians to ass
Externí odkaz:
https://doaj.org/article/993c646b55194fc9978c945da8efb0be
Autor:
Daniela Sorriento
Publikováno v:
Antioxidants, Vol 13, Iss 11, p 1403 (2024)
Reactive oxygen species (ROS) are important signaling molecules, physiologically synthesized by oxygen metabolism [...]
Externí odkaz:
https://doaj.org/article/1da78011135f43cdb6fc38df12958a37
Autor:
D'Agostino, Valerio1,2 (AUTHOR), Sorriento, Angela3,4 (AUTHOR), Cafarelli, Andrea3,4 (AUTHOR), Donati, Danilo5 (AUTHOR), Papalexis, Nicolas1 (AUTHOR), Russo, Alessandro6 (AUTHOR), Lisignoli, Gina7 (AUTHOR), Ricotti, Leonardo3,4 (AUTHOR), Spinnato, Paolo1 (AUTHOR) paolo.spinnato1982@gmail.com
Publikováno v:
Journal of Clinical Medicine. Aug2024, Vol. 13 Issue 16, p4930. 20p.
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:
Nella Prevete, Daniela Sorriento
Publikováno v:
Journal of Molecular Pathology, Vol 4, Iss 4, Pp 318-332 (2023)
A tight association between inflammation and cardiac damage has been extensively recognized. In this review, we will focus on macrophages as key players in the physiology and pathology of the heart and on their role in the functional crosstalk betwee
Externí odkaz:
https://doaj.org/article/2258d0e87dd4429bb15befc41f54d20b
Autor:
N. Lund, H. Wieboldt, L. Fischer, N. Muschol, F. Braun, T. Huber, D. Sorriento, G. Iaccarino, K. Müllerleile, E. Tahir, G. Adam, P. Kirchhof, L. Fabritz, M. Patten
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
IntroductionFabry's disease is an X-linked lysosomal storage disorder caused by reduced activity of α-galactosidase A (GAL), leading to premature death on account of renal, cardiac, and vascular organ failure. Accumulation of the GAL substrate globo
Externí odkaz:
https://doaj.org/article/4243738071ea4ca8a611acc652e137fd
Autor:
Pasquale Mone, Germano Guerra, Angela Lombardi, Maddalena Illario, Antonella Pansini, Anna Marro, Salvatore Frullone, Alessandro Taurino, Daniela Sorriento, Veronica Verri, Guido Iaccarino, Gaetano Santulli
Publikováno v:
Pharmacological Research, Vol 200, Iss , Pp 107055- (2024)
Externí odkaz:
https://doaj.org/article/938d120e66dc43ad9b33ae80ffc5eef8
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