Pubblicazioni

Neoplastic bone marrow invasion:rapid exclusion of hematological disease by flow cytometric routine panels

2023 - BLOOD CELLS, MOLECULES, & DISEASES

Bisegna, Maria Laura; Cordone, Iole; Peragine, Nadia; Milani, Maria Laura; Intoppa, Stefania; de Fabritiis, Paolo; Martelli, Maurizio; De Propris, Maria Stefania

Management goals for type 1 Gaucher disease: a consensus document from the European Working Group on Gaucher Disease.

2018 - BLOOD CELLS, MOLECULES, & DISEASES

Biegstraaten, M.; Cox, T. M.; Belmatoug, N.; Berger, M. G.; Collin-Histed, T.; Di Rocco, M.; Fraga, C.; Giona, F.; Giraldo, P.; Hasanhodzic, M.; Hughes, D. A.; Iversen, P. O.; Kiewiet, A. I.; Lukina, E.; Machaczka, M.; Marinakis, T.; Mengel, E.; Pastores, G. M.; PlÃ¶ckinger, U.; Rosenbaum, H.; Serratrice, C.; Symeonidis, A.; Szer, J.; Timmerman, J.; Tylki-SzymaÅska, A.; Vom Dahl, S.; Weisz Hubshman, M.; Zafeiriou, D. I.; Zimran, A.; Hollak, C. E. M.

Effects of genetic variation in protease activated receptor 4 after an acute coronary syndrome: Analysis from the TRACER trial

2018 - BLOOD CELLS, MOLECULES, & DISEASES

Tricoci, Pierluigi; Neely, Megan; Whitley, Michael J.; Edelstein, Leonard C.; Simon, Lukas M.; Shaw, Chad; Fortina, Paolo; Moliterno, David J.; Armstrong, Paul W.; Aylward, Philip; White, Harvey; Van de Werf, Frans; Jennings, Lisa K.; Wallentin, Lars; Held, Claes; Harrington, Robert A.; Mahaffey, Kenneth W.; Bray, Paul F.

Long-term efficacy and safety results of taliglucerase alfa through 5years in adult treatment-naÃ¯ve patients with Gaucher disease

2016 - BLOOD CELLS, MOLECULES, & DISEASES

Zimran, Ari; DurÃ¡n, Gloria; Giraldo, Pilar; Rosenbaum, Hanna; Giona, Fiorina; Petakov, Milan; Terreros MuÃ±oz, Eduardo; Solorio Meza, Sergio Eduardo; Cooper, Peter A.; Varughese, Sheeba; Alon, Sari; Chertkoff, Raul

Sibling cord blood donor program for hematopoietic cell transplantation: the 20-year experience in the Rome Cord Blood Bank.

2016 - BLOOD CELLS, MOLECULES, & DISEASES

Screnci, M; Murgi, Emilia; Valle, V; Tamburini, A; Pellegrini, Mg; Strano, S; Corona, Francesco; Ambrogi, Eb; Girelli, Gabriella

Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients

2016 - BLOOD CELLS, MOLECULES, & DISEASES

Minelli, A.; Nacci, L.; Valli, R.; Pietrocola, G.; Ramenghi, U.; Locatelli, F.; Brescia, L.; Nicolis, E.; Cipolli, M.; Danesino, C.

Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes

2015 - BLOOD CELLS, MOLECULES, & DISEASES

Radio, FRANCESCA CLEMENTINA; Majore, Silvia; Aurizi, Caterina; Sorge, Fiammetta; Biolcati, Gianfranco; Bernabini, Sara; Giotti, Irene; Torricelli, Francesca; Giannarelli, Diana; De Bernardo, Carmelilia; Grammatico, Paola

SCF-mediated Î³-globin gene expression in adult human erythroid cells is associated with KLF1, BCL11A and SOX6 down-regulation

2015 - BLOOD CELLS, MOLECULES, & DISEASES

Lulli, V; Romania, P; and Morsilli, O; and Ilari, R; and Gabbianelli, M; and Testa, U; and Marziali, G.