Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Irene, Capelli"'
Autor:
Irene Capelli, Roberta Di Costanzo, Valeria Aiello, Sarah Lerario, Paola De Giovanni, Marcello Montevecchi, Davide Cerretani, Vincenzo Donadio, Gaetano La Manna, Renzo Mignani
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Background Fabry disease (FD) is a rare X‐linked lysosomal storage disorder caused by variants in GLA gene leading to deficient α‐galactosidase A enzyme activity. This deficiency leads to the accumulation of glycosphingolipids, particul
Externí odkaz:
https://doaj.org/article/7a800f2ebbec41d495e08d793c3df641
Autor:
Irene Salamon, Elena Biagini, Paolo Kunderfranco, Roberta Roncarati, Manuela Ferracin, Nevio Taglieri, Elena Nardi, Noemi Laprovitera, Luciana Tomasi, Marisa Santostefano, Raffaello Ditaranto, Giovanni Vitale, Elena Cavarretta, Antonio Pisani, Eleonora Riccio, Valeria Aiello, Irene Capelli, Gaetano La Manna, Nazzareno Galiè, Letizia Spinelli, Gianluigi Condorelli
Publikováno v:
Cell Death and Disease, Vol 12, Iss 12, Pp 1-7 (2021)
Abstract Enzyme replacement therapy (ERT) is a mainstay of treatment for Anderson–Fabry disease (AFD), a pathology with negative effects on the heart and kidneys. However, no reliable biomarkers are available to monitor its efficacy. Therefore, we
Externí odkaz:
https://doaj.org/article/536cee0577a8412385a0e329a057c0c8
Autor:
Irene Capelli, Danilo Ribichini, Michele Provenzano, Daniele Vetrano, Valeria Aiello, Giuseppe Cianciolo, Valentina Vicennati, Alessandro Tomassetti, Ginevra Moschione, Sabrina Berti, Uberto Pagotto, Gaetano La Manna
Publikováno v:
Life, Vol 13, Iss 4, p 1061 (2023)
Introduction: Proteinuria is a major risk factor for the progression of chronic kidney disease (CKD). Sodium-glucose cotransporter 2 inhibitors (SGLT2i) demonstrated a nephroprotective and antiproteinuric effect in people with type 2 diabetes (T2DM)
Externí odkaz:
https://doaj.org/article/d35619ae1c574fba9d32c5c678ef7cfa
Autor:
Irene Capelli
Publikováno v:
EtnoAntropologia, Vol 9, Iss 1 (2021)
Having Casablanca as a field site, this article situates heterosexual love and intimacy in the lives of young women experiencing social precariousness, including the uncertain non-status of unmarried mothers. Ethnographic insights broadly question lo
Externí odkaz:
https://doaj.org/article/755bdecdf6a74848a7038f540229c2e2
Autor:
Irene Capelli
Publikováno v:
Health and Human Rights, Vol 21, Iss 2, Pp 33-45 (2019)
Abortion in Morocco is illegal except to safeguard a woman’s life or health. Morocco has put some sexual and reproductive health policies into motion that are in line with the standards defined by the World Health Organization and the United Nation
Externí odkaz:
https://doaj.org/article/6189c05bcb0a4772b1d90de46b0916bd
Autor:
Irene Capelli
Publikováno v:
EtnoAntropologia, Vol 7, Iss 1, Pp 19-36 (2019)
This contribution discusses the deployment of the global category of sexual and reproductive health (SRH) in Morocco by focusing on the case of the pregnancies occurring outside marriage, that do not conform to local social, legal, religious norms. A
Externí odkaz:
https://doaj.org/article/0582f517e4054991aa69a226f28e7602
Autor:
Vera Uliana, Paola Sebastio, Matteo Riva, Diana Carli, Claudio Ruberto, Laura Bianchi, Claudio Graziano, Irene Capelli, Flavio Faletra, Roberto Pillon, Teresa Mattina, Alberto Sensi, Francesco Bonatti, Antonio Percesepe
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Alport syndrome (ATS) is a hereditary progressive hematuric nephropathy associated with sensorineural deafness and ocular abnormalities, which is caused by mutations in the COL4A5 gene (X‐linked ATS) and in two autosomal genes,
Externí odkaz:
https://doaj.org/article/59cf0196e904451d9b61b03c84ea41f4
Autor:
Vilma Mantovani, Sofia Bin, Claudio Graziano, Irene Capelli, Raffaella Minardi, Valeria Aiello, Enrico Ambrosini, Carlotta Pia Cristalli, Alessandro Mattiaccio, Milena Pariali, Sara De Fanti, Flavio Faletra, Enrico Grosso, Rachele Cantone, Elena Mancini, Francesca Mencarelli, Andrea Pasini, Anita Wischmeijer, Nicola Sciascia, Marco Seri, Gaetano La Manna
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common inherited disorders in humans and the majority of patients carry a variant in either PKD1 or PKD2. Genetic testing is increasingly required for diagnosis, pr
Externí odkaz:
https://doaj.org/article/26a65cc630334739b480a8c4a9ee3d31
Autor:
Valeria Corradetti, Giorgia Comai, Matteo Ravaioli, Vania Cuna, Valeria Aiello, Federica Odaldi, Andrea Angeletti, Irene Capelli, Gaetano La Manna
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Cholesterol embolization (CE) is a rare and alarming post-transplant complication, responsible for primary non-function (PNF) or delayed graft function (DGF). Its incidence is expected to rise due to increasingly old donors and recipients and the ext
Externí odkaz:
https://doaj.org/article/c6969e41adad474aa2ab47b180d70402
Autor:
Irene Capelli
Publikováno v:
L’Année du Maghreb, Vol 17, Pp 83-99 (2017)
In Morocco, pregnancies and births outside marriage are the subject of many initiatives, especially in the field of non-governmental organizations. Many of these call for changes in family law to ensure that children born out of wedlock are not discr
Externí odkaz:
https://doaj.org/article/c4042f06537844e69216aec622f5e7ac