Villegas, Ana; Ropero, Paloma; González, Fernando-Ataulfo; Morado, Marta; Menor, María; de-la-Iglesia, Silvia; López-Rubio, Montserrat; Salido-Fiérrez, Eduardo-José; Abio, Mariola; Senent, María-Leonor; Recasens, Valle; Vagace, José-Manuel; Fonte, Cristina; Hernández-Rivas, Jesus-María; Raya, José-María; Rios, Pablo; Peri, Valeria-Luciana; Herrera, Keneth-A; Tenorio, María-Concepción; Lo-Riso, Laura; Tena, Juan; Molina, María-Angustias; Vara, Miriam; Rodríguez, Isabel; Ricard, Pilar; Gómez, Miguel; Dusacovschi, Oana-Popa; Vidan, Julia-María; Groiss, Jorge; Ferre, Oscar; Orbe, Irene; López, Rosa-María; Ugalde, Nazaret; Hidalgo, Manuela-Ines; Hinojosa, Cristina; Rodríguez, Ana-Isabel; Herrera, Esther; Muruzabal, María-Josefa; del-Carmen-Hernández, María; Marco, Josefa-Esperanza; Benavente, Celina
(WILEY, 2026-06-02)
BACKGROUND: Beta-thalassemia is a genetically heterogeneous hemoglobinopathy with marked clinical variability. In Spain, comprehensive nationwide data on transfusion-dependent beta-thalassemia (TDT) remain limited, ...