Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renata Riolo"'
Autor:
Irene Simonetta, Renata Riolo, Federica Todaro, Vincenzo Donadio, Alex Incensi, Salvatore Miceli, Paolo Colomba, Giovanni Duro, Antonino Tuttolomondo
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/c484d23f8b7247efa94004343fba4687
Autor:
Alessandro Del Cuore, Rosaria Maria Pipitone, Alessandra Casuccio, Marco Maria Mazzola, Maria Grazia Puleo, Gaetano Pacinella, Renata Riolo, Carlo Maida, Tiziana Di Chiara, Domenico Di Raimondo, Rossella Zito, Giulia Lupo, Luisa Agnello, Gabriele Di Maria, Marcello Ciaccio, Stefania Grimaudo, Antonino Tuttolomondo
Publikováno v:
Cardiovascular Diabetology, Vol 22, Iss 1, Pp 1-18 (2023)
Abstract Background Diabetic foot is a significant cause of morbidity in diabetic patients, with a rate that is approximately twice that of patients without foot ulcers. “Metabolic memory” represents the epigenetic changes induced by chronic hype
Externí odkaz:
https://doaj.org/article/386b2ade14af4950af3fa58cfa8dafcf
Autor:
Irene Simonetta, Renata Riolo, Federica Todaro, Vincenzo Donadio, Alex Incensi, Salvatore Miceli, Paolo Colomba, Giovanni Duro, Antonino Tuttolomondo
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Anderson–Fabry disease (AFD) is an X-linked disease that results from reduced activity of the enzyme galactosidase alpha (GLA). When the GLA gene sequence is altered by mutations that alter the normal DNA sequence, variants of the alpha
Externí odkaz:
https://doaj.org/article/33ade6485def44aeb5ff52fc177b417a
Autor:
Antonino Tuttolomondo, Irene Baglio, Renata Riolo, Federica Todaro, Gaspare Parrinello, Salvatore Miceli, Irene Simonetta
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 1, p 61 (2023)
Fabry disease (FD) is a recessive monogenic disease linked to chromosome X due to more than two hundred mutations in the alfa-galactosidase A (GLA) gene. Modifications of the GLA gene may cause the progressive accumulation of globotriaosylceramide (G
Externí odkaz:
https://doaj.org/article/b8a52d85e644435a94d6f30da5db1c30
Autor:
Vittoriano Della Corte, Renata Riolo, Stefania Scaglione, Rosaria Pecoraro, Antonino Tuttolomondo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13411 (2023)
In recent years, the field of venous thromboembolism has undergone numerous innovations, starting from the recent discoveries on the role of biomarkers, passing through the role of metabolomics in expanding our knowledge on pathogenic mechanisms, whi
Externí odkaz:
https://doaj.org/article/aa1c954d86264f6ca344628b62aeba59
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 16002 (2022)
Human nutrition is a relatively new science based on biochemistry and the effects of food constituents. Ancient medicine considered many foods as remedies for physical performance or the treatment of diseases and, since ancient times, especially Gree
Externí odkaz:
https://doaj.org/article/4e293f34b9a64c2ba9881d1bc870d73b
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 13, p 7136 (2022)
Cerebral small vessel disease (CSVD) is one of the most important causes of vascular dementia. Immunosenescence and inflammatory response, with the involvement of the cerebrovascular system, constitute the basis of this disease. Immunosenescence iden
Externí odkaz:
https://doaj.org/article/db1374f93df341639676e3dbe9de02b8
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 6, p 3018 (2022)
Migraine is a hereditary disease, usually one-sided, sometimes bilateral. It is characterized by moderate to severe pain, which worsens with physical activity and may be associated with nausea and vomiting, may be accompanied by photophobia and phono
Externí odkaz:
https://doaj.org/article/2bafb9a56fc743cdbaa94be2a369a6fa
Autor:
Antonino Tuttolomondo, Irene Simonetta, Renata Riolo, Federica Todaro, Tiziana Di Chiara, Salvatore Miceli, Antonio Pinto
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 18, p 10088 (2021)
Anderson–Fabry disease (AFD) is a rare disease with an incidenceof approximately 1:117,000 male births. Lysosomal accumulation of globotriaosylceramide (Gb3) is the element characterizing Fabry disease due to a hereditary deficiency α-galactosidas
Externí odkaz:
https://doaj.org/article/e6f22f7dfb484928a67e7e51c5a8edcb
Autor:
Alessandro Del Cuore, Rosaria Maria Pipitone, Alessandra Casuccio, Marco Mazzola, Maria Grazia Puleo, Gaetano Pacinella, Renata Riolo, Carlo Maida, Tiziana Chiara, Domenico Raimondo, Rossella Zito, Giulia Lupo, Luisa Agnello, Marcello Ciaccio, Stefania Grimaudo, Antonino Tuttolomondo
Background: Diabetic foot is a significant cause of morbidity in diabetic patients, with a rate that is approximatelytwice that of patients without foot ulcers. “Metabolic memory” represents the epigenetic changes induced by chronic hyperglycaemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa45d1b9a1dc584f97d59899166f490a
https://hdl.handle.net/10447/594093
https://hdl.handle.net/10447/594093