Secondary myeloid neoplasms (sMNs) remain the most serious long-term complications in patients with aplastic anemia (AA) and paroxysmal nocturnal hemoglobinuria (PNH). However, sMNs lack specific predictors, dedicated surveillance measures, and early therapeutic interventions.

Gurnari, C., Pagliuca, S., Prata, P.h., Galimard, J., Catto, L., Larcher, L., et al. (2023). Clinical and molecular determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria. JOURNAL OF CLINICAL ONCOLOGY, 41(1), 132-142 [10.1200/JCO.22.00710].

Clinical and molecular determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria

Gurnari, Carmelo;Voso, Maria Teresa;
2023-09-02

Abstract

Secondary myeloid neoplasms (sMNs) remain the most serious long-term complications in patients with aplastic anemia (AA) and paroxysmal nocturnal hemoglobinuria (PNH). However, sMNs lack specific predictors, dedicated surveillance measures, and early therapeutic interventions.
2-set-2023
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/15 - MALATTIE DEL SANGUE
English
Gurnari, C., Pagliuca, S., Prata, P.h., Galimard, J., Catto, L., Larcher, L., et al. (2023). Clinical and molecular determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria. JOURNAL OF CLINICAL ONCOLOGY, 41(1), 132-142 [10.1200/JCO.22.00710].
Gurnari, C; Pagliuca, S; Prata, Ph; Galimard, J; Catto, Lfb; Larcher, L; Sebert, M; Allain, V; Patel, Bj; Durmaz, A; Pinto, Al; Inacio, Mcb; Hernandez...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/307761
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