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Sfoglia per Rivista  HAEMATOLOGICA

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Mostrati risultati da 1 a 20 di 76
Titolo Data di pubblicazione Autore(i) File
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 1-gen-1999 Perrotta, Silverio; Iolascon, A; Polito, R; D'Urzo, G; Conte, Ml; MIRAGLIA DEL GIUDICE, Emanuele
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 1-gen-2007 Zdebska, E; Iolascon, A; Spychalska, J; Perrotta, Silverio; Lanzara, C; SMOLENSKA SYM, G; Koscielak, J.
Altered constitutive and activation-induced expression of CD95 by B- and T-cells in B-cell chronic lymphocytic leukemia 1-gen-2002 DE FANIS, U; DALLA MORA, Liliana; Romano, Ciro Pasquale; Sellitto, A; Tirelli, Armando; Lucivero, Giacomo
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 1-gen-1997 MIRAGLIA DEL GIUDICE, Emanuele; Francese, M; Polito, R; Nobili, Bruno; Iolascon, A; Perrotta, Silverio
Are low doses of lenalidomide effective in 5q- syndrome? 1-gen-2011 Guastafierro, Salvatore; Ferrara, Mg; Sica, A; Parascandola, Rr; Falcone, U.
[Autologous bone marrow transplantation without cryopreservation after megadoses of oncolytic chemotherapy. Pilot study in 18 cases] 1-gen-1983 Carella, Am; Santini, G; Frassoni, F; Giordano, Dario Ranieri; Congiu, A; Nati, S; Risso, M; Cerri, R; Occhini, D; Damasio, E.
B-cell lymphoproliferative disease and acute myeloid leukemia in one patient 1-gen-2013 Falcone, U; Ferrara, Mg; Parascandola, Rr; Sica, A; Di Martino, A; Guastafierro, Salvatore
Beta-endorphin and red blood cell filtration 1-gen-1987 Tirelli, Armando; Coppola, L; Giunta, Riccardo; Ceriello, A.
{beta}-spectrinBari: a truncated {beta}-chain responsible for dominant hereditary spherocytosis. 1-gen-2009 Perrotta, Silverio; DELLA RAGIONE, Fulvio; Rossi, Francesca; Avvisati, R.; DI PINTO, D.; DE MIERI, G.; Scianguetta, S.; Mancusi, S.; DE FALCO, L.; Marano, V.; Iolascon, A.
Bisphosphonates and jaw osteonecrosis in myeloma patients 1-gen-2005 Colella, Giuseppe; Guastafierro, Salvatore; Celentano, M; Correale, P; Ferrara, Mg; Tirelli, A.
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 1-gen-2014 Casale, Maddalena; Citarella, S; Amendola, G; Iolascon, Giovanni; Costantini, S; De Michele, E; Pugliese, U; Tartaglione, I; Gallicola, F; Cinque, P; Filosa, A; Perrotta, Silverio
BORTEZOMIB INDUCES APOPTOSIS IN BOTH RESTING AND CD40-ACTIVATED CLL B CELLS 1-gen-2009 Simeone, L; Chiurazzi, F; Avilia, S; Romano, Ciro Pasquale; Sellitto, A; DE FANIS, U; Lucivero, Giacomo; Rotoli, B.
C1 inhibitor (C1 INH) and platelet aggregation 1-gen-1988 Coppola, L; Verrazzo, G; Giunta, Riccardo; Tirelli, Armando
Cell cycle regulation and human leukemias: the role of p16INK4 gene inactivation in the development of human acute lymphoblastic leukemia 1-gen-1995 DELLA RAGIONE, Fulvio; Mercurio, C; Iolascon, A.
Cell division cycle manipulation and cancer treatment: a solid promise or just a dream? 1-gen-2002 Iolascon, A; DELLA RAGIONE, Fulvio
Circulating immune complexes in malignant lymphomas 1-gen-1984 Castello, G; DALLA MORA, Liliana; Abate, G; Comella, P; Perna, M; Pergola, M; Zarrilli, D.
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 1-gen-2012 Noris, P; Perrotta, Silverio; Bottega, R; Pecci, A; Melazzini, F; Civaschi, E; Russo, S; Magrin, S; Loffredo, G; Di Salvo, V; Russo, G; Casale, Maddalena; De Rocco, D; Grignani, C; Cattaneo, M; Baronci, C; Dragani, A; Albano, V; Jankovic, M; Scianguetta, S; Savoia, A; Balduini, C. L.
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 1-gen-2011 Rossi, Francesca; Mancusi, S; Bellini, Giulia; Roberti, D; Punzo, F; Vetrella, S; Matarese, Sm; Nobili, Bruno; Maione, Sabatino; Perrotta, Silverio
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects 1-gen-1996 Iolascon, A; D'Agostaro, G; Perrotta, Silverio; Izzo, P; Tavano, R; MIRAGLIA DEL GIUDICE, Emanuele
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 1-gen-2013 Perrotta, Silverio; Stiehl, Daniel P; Punzo, Francesca; Scianguetta, Saverio; Borriello, Adriana; Bencivenga, Debora; Casale, Maddalena; Nobili, Bruno; Fasoli, Silvia; Balduzzi, Adriana; Cro, Lilla; Nytko, Katarzyna J; Wenger, Roland H.; DELLA RAGIONE, Fulvio
Mostrati risultati da 1 a 20 di 76
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