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Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.
Fortugno C, Galea E, Cantaffa R, Gigliotti F, Fabiano RL, Talarico V, Raiola G, Galati MC. Fortugno C, et al. Among authors: galea e. Pediatr Hematol Oncol. 2021 Mar;38(2):184-190. doi: 10.1080/08880018.2020.1829219. Epub 2020 Nov 2. Pediatr Hematol Oncol. 2021. PMID: 33136529 No abstract available.
A Novel Bispecific T-Cell Engager (CD1a x CD3ε) BTCE Is Effective against Cortical-Derived T Cell Acute Lymphoblastic Leukemia (T-ALL) Cells.
Riillo C, Caracciolo D, Grillone K, Polerà N, Tuccillo FM, Bonelli P, Juli G, Ascrizzi S, Scionti F, Arbitrio M, Lopreiato M, Siciliano MA, Sestito S, Talarico G, Galea E, Galati MC, Pensabene L, Loprete G, Rossi M, Ballerini A, Gentile M, Britti D, Di Martino MT, Tagliaferri P, Tassone P. Riillo C, et al. Among authors: galea e. Cancers (Basel). 2022 Jun 11;14(12):2886. doi: 10.3390/cancers14122886. Cancers (Basel). 2022. PMID: 35740552 Free PMC article.
106 results