Zobrazeno 1 - 10
of 635
pro vyhledávání: '"Ali T. Taher"'
Autor:
Ali T. Taher, Yasser Wali, Maria Cecilia Cruz, Pimlak Charoenkwan, Yesim Aydinok, Olena Werner, Sameera Govindaraju, Fabian Romen, Vip Viprakasit
Publikováno v:
Haematologica, Vol 109, Iss 5 (2023)
CALYPSO (clinicaltrials gov. Identifier: NCT02435212), a randomized, open-label, multicenter, phase II study evaluated the compliance, clinical benefits, and safety of deferasirox granules and dispersible tablets (DT) in pediatric patients with iron
Externí odkaz:
https://doaj.org/article/3ac9ea4995e4411f82eb7796e45ca40e
Autor:
Ali T. Taher, Vip Viprakasit, Maria Domenica Cappellini, Antonio Giulio Piga, John B. Porter, Thomas D. Coates, Khaled M. Musallam, Gian Luca Forni, Jeevan K. Shetty, Marija Bosilkovska Weisskopf, Richard Wei, Wen-Ling Kuo, Antonis Kattamis
Publikováno v:
HemaSphere, Vol 7, p e45673ef (2023)
Externí odkaz:
https://doaj.org/article/932d22a052d143f1b78c75bc9959594c
Autor:
Thomas D. Coates, Maria Domenica Cappellini, Sujit Sheth, Kevin H.M. Kuo, Antonio Giulio Piga, Antonis Kattamis, Martina Perin, Frederik Lersch, Jeevan K. Shetty, Yinzhi Lai, Wen-Ling Kuo, Ali T. Taher
Publikováno v:
HemaSphere, Vol 7, p e882049a (2023)
Externí odkaz:
https://doaj.org/article/8efb778ff67647b0a10b1b13d0f8fc95
Autor:
Khaled M. Musallam, Sujit Sheth, Maria Domenica Cappellini, Antonis Kattamis, Kevin H. M. Kuo, Ali T. Taher
Publikováno v:
Therapeutic Advances in Hematology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/e8ac36d1382840688a5a2994b60d7f90
Publikováno v:
Thalassemia Reports, Vol 13, Iss 1, Pp 38-50 (2023)
Beta thalassemia is an inherited disorder resulting in abnormal or decreased production of hemoglobin, leading to hemolysis and chronic anemia. The long-term complications can affect multiple organ systems, namely the liver, heart, and endocrine. Myo
Externí odkaz:
https://doaj.org/article/fc3b3527f045428292e6679dcb2072e1
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, Ali T. Taher, Maria Domenica Cappellini, Olivier Hermine, Kevin H. M. Kuo, Sujit Sheth, Vip Viprakasit, John B. Porter
Publikováno v:
HemaSphere, Vol 6, Iss 12, p e806 (2022)
Externí odkaz:
https://doaj.org/article/26beb4139c504eb29d724860a9c4d533
Autor:
Achille Iolascon, Stefano Rivella, Nicholas P. Anagnou, Clara Camaschella, Dorine Swinkels, Martina U. Muckenthaler, Graça Porto, Wilma Barcellini, Immacolata Andolfo, Antonio M. Risitano, Antonis Kattamis, Maria Domenica Cappellini, Ali T. Taher, Lucia De Franceschi, David Rees, Roberta Russo, Hannah Tamary, Reinhard Stauder, Domenico Girelli
Publikováno v:
HemaSphere, Vol 5, Iss 7 (2021)
Externí odkaz:
https://doaj.org/article/0fcc05f31b0f42ca924d9b2aa4209d82
Autor:
Georges El Hasbani, Ali T. Taher, Alain S. Abi-Ghanem, Samer Nassif, Abdul Rahman Bizri, Imad Uthman
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
Diffuse large B-cell lymphoma (DLBCL) commonly presents with systemic manifestations including fever, weight loss, and night sweats. Uncommonly, patients with DLBCL can present with musculoskeletal manifestations mimicking polymyalgia rheumatica (PMR
Externí odkaz:
https://doaj.org/article/ecdfb80b96e24b8492cb184e230358cc
Autor:
Rayan Bou-Fakhredin, Lucia De Franceschi, Irene Motta, Maria Domenica Cappellini, Ali T. Taher
Publikováno v:
Pharmaceuticals, Vol 15, Iss 6, p 753 (2022)
A significant amount of attention has recently been devoted to the mechanisms involved in hemoglobin (Hb) switching, as it has previously been established that the induction of fetal hemoglobin (HbF) production in significant amounts can reduce the s
Externí odkaz:
https://doaj.org/article/1aa966635fca4e3990f2c276489de935