Zobrazeno 1 - 4
of 4
pro vyhledávání: '"A Glenthj"'
Autor:
KH Kuo, H Al-Samkari, Y Aydinok, M Besser, S Gheuens, G Luna, A Glenthj, AS Goh, A Kattamis, SR Loggetto, KM Musallam, P Ricchi, E Salido-Fiérrez, S Sheth, V Viprakasit, MD Cappellini, AT Taher
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S34-S35 (2024)
Background: Thalassemia, a group of inherited disorders characterized by ineffective erythropoiesis and chronic hemolytic anemia, is associated with wide-ranging impacts on health-related quality of life (HRQoL), such as impaired physical functioning
Externí odkaz:
https://doaj.org/article/50717b761b4d4b66bdbad276d68442b5
Autor:
AT Taher, H Al-Samkari, Y Aydinok, M Besser, G Luna, S Gheuens, A Glenthj, AS Goh, A Kattamis, SR Loggetto, KM Musallam, P Ricchi, E Salido-Fiérrez, S Sheth, V Viprakasit, MD Cappellini, KH Kuo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S32-S33 (2024)
Background: In thalassemia, ATP production in erythroid cells is too low to meet the demand of oxidative stress and ensuing cellular damage; this leads to ineffective erythropoiesis (IE) and chronic hemolytic anemia. Guidelines for non–transfusion-
Externí odkaz:
https://doaj.org/article/c8f32b3099bd4cf3bf04a8b5b36f0ab4
Autor:
Kuo, KH, Al-Samkari, H, Aydinok, Y, Besser, M, Gheuens, S, Luna, G, Glenthj, A, Goh, AS, Kattamis, A, Loggetto, SR, Musallam, KM, Ricchi, P, Salido-Fiérrez, E, Sheth, S, Viprakasit, V, Cappellini, MD, Taher, AT
Publikováno v:
In Hematology, Transfusion and Cell Therapy October 2024 46 Supplement 4:S34-S35
Autor:
Taher, AT, Al-Samkari, H, Aydinok, Y, Besser, M, Luna, G, Gheuens, S, Glenthj, A, Goh, AS, Kattamis, A, Loggetto, SR, Musallam, KM, Ricchi, P, Salido-Fiérrez, E, Sheth, S, Viprakasit, V, Cappellini, MD, Kuo, KH
Publikováno v:
In Hematology, Transfusion and Cell Therapy October 2024 46 Supplement 4:S32-S33