Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Walter Addario Pollina"'
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:
Rita Barone, Paolo Ricchi, Laura Pistoia, Alessia Pepe, Salvatore Scondotto, Antonella Meloni, Saqib Hussain Ansari, Fedele Bonifazi, Aldo Filosa, Sylvia T. Singer, Aurelio Maggio, Mahmoud Hajipour, Shahina Daar, Gabriella Dardanoni, Amal El-Beshlawy, J F Borgio, Elliott Vichinsky, Vito Di Marco, Lorella Pitrolo, Walter Addario Pollina, Angela Vitrano, Mehran Karimi, Massimiliano Sacco, Adriana Ceci
Publikováno v:
Blood. 136:15-16
Background Thalassemia Syndromes (TS) are commonly classified as transfusion-dependent-thalassemia (TDT) or non-transfusion-dependent thalassemia (NTDT) at diagnosis on the basis of requirement for lifelong regular transfusion therapy for survival. H
Autor:
Paolo Rigano, Sana Al-Jarrash, Shahina Daar, Aurelio Maggio, Paolo Moi, Massimiliano Sacco, Marie Charlotte Bouesseau, Farrukh Shah, Vito Di Marco, Antonella Meloni, Mahmoud Yassin, Amal El-Beshlawy, Aldo Filosa, Saqib Hussain Ansari, Mahmoud Hajipour, Soteroula Christou, Zaki A. Naserullah, Laura Pistoia, Vip Viprakasit, Sylvia Titi Singer, Olivier Hermine, Salvatore Scondotto, Gabriella Dardanoni, Alessia Pepe, Suthat Fucharoen, Jianpei Fang, Adriana Ceci, Paolo Ricchi, Walter Addario Pollina, Angela Vitrano, Mehran Karimi, Kunle Adekile, Lorella Pitrolo, Alok Srivastava, Ibrahim Mohd Hishamshah, Elliott Vichinsky
Publikováno v:
SSRN Electronic Journal.
Background: Classification of phenotype severity in patients with beta-thalassaemia has so far relied mainly on expert opinion using parameters of genotype, clinical features at diagnosis, and transfusion requirement. The aim of this study was to use
Autor:
Walter Addario Pollina, Angela Vitrano, Mehran Karimi, Vito Di Marco, Shahina Daar, Massimiliano Sacco, Aldo Filosa, Mahmoud Hajipour, Alessia Pepe, Adriana Ceci, Rosario Di Maggio, Elliott Vichinsky, Antonella Meloni, Gabriella Dardanoni, Sylvia T. Singer, Paolo Ricchi, Saqib Hussain Ansari, J F Borgio, Amal El-Beshlawy, Aurelio Maggio, Salvatore Scondotto
Publikováno v:
Blood. 134:2225-2225
Introduction Thalassemia Syndromes (TS) are a group of inherited haemoglobin disorders characterized by different phenotype severity falling among heterozygote state, no transfusion dependent thalassemia (NTDT) and transfusion dependent Thalassemia (