Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Rayan Bou‐Fakhredin"'
Autor:
Achille Iolascon, Immacolata Andolfo, Roberta Russo, Mayka Sanchez, Fabiana Busti, Dorine Swinkels, Patricia Aguilar Martinez, Rayan Bou‐Fakhredin, Martina U. Muckenthaler, Sule Unal, Graça Porto, Tomas Ganz, Antonis Kattamis, Lucia De Franceschi, Maria Domenica Cappellini, Malcolm G. Munro, Ali Taher, from EHA‐SWG Red Cell and Iron
Publikováno v:
HemaSphere, Vol 8, Iss 7, Pp n/a-n/a (2024)
Abstract Iron is an essential nutrient and a constituent of ferroproteins and enzymes crucial for human life. Generally, nonmenstruating individuals preserve iron very efficiently, losing less than 0.1% of their body iron content each day, an amount
Externí odkaz:
https://doaj.org/article/1110b685ccc94b95b52d4d0674c31370
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
Autor:
Dimitrios Farmakis, John Porter, Ali Taher, Maria Domenica Cappellini, Michael Angastiniotis, Androulla Eleftheriou, for the 2021 TIF Guidelines Taskforce, Ali Alassaf, Emanuele Angelucci, Yesim Aydinok, Rayan Bou-Fakhredin Rayan, Loris Brunetta, George Constantinou, Shahina Daar, Vincenzo De Sanctis, Geoffrey Dusheiko, Riyad Elbard, Perla Eleftheriou, Panos Englezos, Dru Haines, Faiez N Hattab, George Kaltsounis, Antonios Kattamis, John Koskinas, Navdeep Kumar, Andreas Kulozik, Andreas Kyriakou, Aurelio Maggio, Roanna Maharai, Lauren Mednick, Eleni Michalaki, Wendy Murphy, Lena Oevermann, Raffaella Origa, Penelope-Georgia Papayanni, Constantina Politis, Farukh Shah, Anton Skafi, Nikos Skordis, Pietro Sodani, Ashraf Soliman, Seni Subair, Maria Tampaki, Sara Trompeter, Shobha Tuli, Malcolm Walker, Robert Yamashita, Evangelia Yannaki, Anne Yardumian
Publikováno v:
HemaSphere, Vol 6, Iss 8, p e732 (2022)
Beta-thalassemia and particularly its transfusion-dependent form (TDT) is a demanding clinical condition, requiring life-long care and follow-up, ideally in specialized centers and by multidisciplinary teams of experts. Despite the significant progre
Externí odkaz:
https://doaj.org/article/e09c27ab622646e18fe28c7d0ec0779e
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
Autor:
Rayan Bou-Fakhredin, Lucia De Franceschi, Irene Motta, Assaad A. Eid, Ali T. Taher, Maria Domenica Cappellini
Publikováno v:
Antioxidants, Vol 11, Iss 5, p 967 (2022)
β-thalassemia and sickle cell disease (SCD) are inherited hemoglobinopathies that result in both quantitative and qualitative variations in the β-globin chain. These in turn lead to instability in the generated hemoglobin (Hb) or to a globin chain
Externí odkaz:
https://doaj.org/article/e5a942b5890c467f9cf08bebc58073f7
Autor:
Ali T. Taher, Achille Iolascon, Charbel F. Matar, Rayan Bou-Fakhredin, Lucia de Franceschi, Maria Domenica Cappellini, Wilma Barcellini, Roberta Russo, Immacolata Andolfo, Paul Tyan, Beatrice Gulbis, Yesim Aydinok, Nicholas P. Anagnou, Gabriela Amstad Bencaiova, Hannah Tamary, Patricia Aguilar Martinez, Gianluca Forni, Raffaele Vindigni, on behalf of the EHA Scientific Working Group on “Red Cells, Iron”
Publikováno v:
HemaSphere, Vol 4, Iss 4, p e446 (2020)
Abstract. Rare inherited anemias are a subset of anemias caused by a genetic defect along one of the several stages of erythropoiesis or in different cellular components that affect red blood cell integrity, and thus its lifespan. Due to their low pr
Externí odkaz:
https://doaj.org/article/ebe1f92cc10e4f88b146f066ed638641
Publikováno v:
Thalassemia Reports, Vol 8, Iss 1 (2018)
Iron overload (IOL) is highly prevalent among patients with hemoglobinopathies; both transfusion dependent thalassemia (TDT) and non-transfusion dependent thalassemia (NTDT). Whether IOL is secondary to regular transfusions like in TDT, or develops f
Externí odkaz:
https://doaj.org/article/e0a737929f07474181cd8574928634a1
Publikováno v:
Hematology/Oncology Clinics of North America. 37:341-351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17554e2cee046917c0da77e9ba6112b5
https://doi.org/10.1016/j.hoc.2022.12.005
https://doi.org/10.1016/j.hoc.2022.12.005
Publikováno v:
Hematology/Oncology Clinics of North America. 37:449-462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b0b86f9e7616432d057800832bae7e0
https://doi.org/10.1016/j.hoc.2022.12.010
https://doi.org/10.1016/j.hoc.2022.12.010
Publikováno v:
Expert Review of Hematology. 15:1055-1061
Pregnancy in women with sickle cell disease (SCD) has been identified as high risk owing to increased incidence of materno-fetal complications across various studies and reports. These complications include consequences related to the underlying hemo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1a4ac62c89eab3234a5eef3d0c4eb5d
https://doi.org/10.1080/17474086.2022.2151432
https://doi.org/10.1080/17474086.2022.2151432