Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Angela Vitrano"'
Autor:
Fabiana D’Esposito, Viviana Randazzo, Maria Igea Vega, Gabriella Esposito, Paolo Enrico Maltese, Salvatore Torregrossa, Paola Scibetta, Florinda Listì, Caterina Gagliano, Lucia Scalia, Antonino Pioppo, Antonio Marino, Marco Piergentili, Emanuele Malvone, Tiziana Fioretti, Angela Vitrano, Maria Piccione, Teresio Avitabile, Francesco Salvatore, Matteo Bertelli, Ciro Costagliola, Maria Francesca Cordeiro, Aurelio Maggio, Elena D’Alcamo
Publikováno v:
Medicina, Vol 60, Iss 2, p 254 (2024)
Background and Objectives. Retinitis pigmentosa (RP) is the most common inherited rod–cone dystrophy (RCD), resulting in nyctalopia, progressive visual field, and visual acuity decay in the late stages. The autosomal dominant form (ADRP) accounts f
Externí odkaz:
https://doaj.org/article/83b2da28abdc4e8788f1ab43b53ceb6c
Autor:
Simona Raso, Meloni Antonella, Anna Spasiano, Andrea Salvo, Maria Grazia Roberti, Valerio Cecinati, Angela Ciancio, Amalia Acquafredda, Ilaria Fotzi, Rosamaria Rosso, Marilena Serra, Costanza Bosi, Calogera Gerardi, Mariasanta Napolitano, Vincenzo Sucato, Rosario DI Maggio, Angela Vitrano, Filippo Cademartiri, Aurelio Maggio
Publikováno v:
HemaSphere, Vol 7, p e581019c (2023)
Externí odkaz:
https://doaj.org/article/f85c4e53d0aa44e2954e86607182bf88
Autor:
Rita Barone, Bianca Magro, Angela Vitrano, Alessandro Inzerillo, Rossellina Rosso, Maria Grazia Bavetta, Giorgio Fusco, Mirko Olivo, Lorella Pitrolo, Antonino Giangreco, Rosario DI Maggio, Disma Renda, Angela Rao Camemi, Salvatore Gruttadauria, Aurelio Maggio
Publikováno v:
HemaSphere, Vol 7, p e4371393 (2023)
Externí odkaz:
https://doaj.org/article/ff3812ad92a743c793958e20e6bdd850
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
Autor:
Angela Vitrano, Khaled M. Musallam, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo Filosa, Paolo Ricchi, Adriana Ceci, Shahina Daar, Efthymia Vlachaki, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio, International Working Group on Thalassemia (IWG-THAL)
Publikováno v:
Thalassemia Reports, Vol 12, Iss 1, Pp 14-23 (2022)
In this work, we aimed to establish subgroups of clinical severity in a global cohort of β-thalassemia through unsupervised random forest (RF) clustering. We used a large global dataset of 7910 β-thalassemia patients and evaluated 19 indicators of
Externí odkaz:
https://doaj.org/article/aa15c48822b849b987d37e3cf47bfde0
Autor:
Khaled M. Musallam, Angela Vitrano, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo Filosa, Paolo Ricchi, Adriana Ceci, Shahina Daar, Efthymia Vlachaki, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio
Publikováno v:
Haematologica, Vol 106, Iss 9 (2021)
Externí odkaz:
https://doaj.org/article/f8aa168aaecb4973892659488df605a9
Autor:
Maria Concetta Renda, Angela Vitrano, Massimo Attanasio, Emanuela Fecarotta, Angela Piazza, Antonino Giambona, Germana Fiorentino, Disma Renda, Paolo Rigano, Giuseppina Calvaruso, Filippo Cassarà, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 2, Iss 1, Pp e2-e2 (2012)
Nonsense-mediated mRNA decay (NMD) is a surveillance system to prevent the synthesis of non-functional proteins. In β-thalassemia, NMD may have a role in clinical outcome. An example of premature translation stop codons appearing for the first time
Externí odkaz:
https://doaj.org/article/253c4429dfb54491838a88d4ae90d0b7
Autor:
Angela Vitrano, Khaled M. Musallam, Antonella Meloni, Mehran Karimi, Shahina Daar, Paolo Ricchi, Silvia Costantini, Efthymia Vlachaki, Vito Di Marco, Amal El-Beshlawy, Mahmoud Hajipour, Saqib Hussain Ansari, Aldo Filosa, Adriana Ceci, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Filippo Cademartiri, Sebastiano Addario Pollina, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio
Publikováno v:
Blood cells, moleculesdiseases. 99
A prognostic scoring system that can differentiate β-thalassemia patients based on mortality risk is lacking. We analysed data from 3145 β-thalassemia patients followed through a retrospective cohort design for the outcome of death. An a priori lis
Autor:
Aurelio Maggio, Vito Di Marco, Mahmoud Hajipour, Shahina Daar, Saqib Hussain Ansari, Amal El-Beshlawy, Gabriella Dardanoni, Salvatore Scondotto, Alessia Pepe, Aldo Filosa, Sylvia T. Singer, Zaki A Naserullah, Fedele Bonifazi, Antonella Meloni, Elliott Vichinsky, Walter Addario Pollina, Angela Vitrano, Mehran Karimi, Adriana Ceci, Paolo Ricchi
Publikováno v:
British Journal of Haematology. 192:626-633
The thalassaemia syndromes (TS) show different phenotype severity. Developing a reliable, practical and global tool to determine disease severity and tailor treatment would be of great value. Overall, 7910 patients were analysed with the aim of const
Autor:
Gabriella Dardanoni, Amal El-Beshlawy, Aldo Filosa, Khaled M. Musallam, Fedele Bonifazi, Shahina Daar, Zaki A Naserullah, Vito Di Marco, Ali T. Taher, Saqib Hussain Ansari, Sebastiano Addario Pollina, Angela Vitrano, Vijay G. Sankaran, Mahmoud Hajipour, Alessia Pepe, Mehran Karimi, Elliott Vichinsky, Paolo Ricchi, Antonella Meloni, Sylvia T. Singer, Salvatore Scondotto, Aurelio Maggio, Adriana Ceci, Efthymia Vlachaki
In β-thalassaemia, the severity of inherited β-globin gene mutations determines the severity of the clinical phenotype at presentation and subsequent transfusion requirements. However, data on associated long-term outcomes remain limited. We analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3947d781a5ee1c5c3de86999bd96b0c1
http://hdl.handle.net/11577/3414716
http://hdl.handle.net/11577/3414716
Autor:
Angela, Vitrano, Musallam, Khaled M., Antonella, Meloni, Sebastiano Addario Pollina, Mehran, Karimi, Amal, El-Beshlawy, Mahmoud, Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo, Filosa, Paolo, Ricchi, Adriana, Ceci, Shahina, Daar, Efthymia, Vlachaki, Sylvia Titi Singer, Naserullah, Zaki A., Pepe, Alessia, Salvatore, Scondotto, Gabriella, Dardanoni, Fedele, Bonifazi, Sankaran, Vijay G., Elliott, Vichinsky, Taher, Ali T., Aurelio, Maggio
Publikováno v:
Thalassemia Reports; Volume 12; Issue 1; Pages: 14-23
In this work, we aimed to establish subgroups of clinical severity in a global cohort of β-thalassemia through unsupervised random forest (RF) clustering. We used a large global dataset of 7910 β-thalassemia patients and evaluated 19 indicators of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e9da03b71d22d3258b3a5018a6bbfb
https://hdl.handle.net/11577/3477250
https://hdl.handle.net/11577/3477250