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Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG) 1-gen-2000 BEAUCHAMP NICOUD, A; Morle, L; Lutz, Hu; Stammler, P; Agulles, O; PETERMANN KHDER, R; Iolascon, A; Perrotta, Silverio; Cynober, T; Tchernia, G; Delaunay, J; BAUDIN CREUZA, V.
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 1-gen-1992 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Fiorelli, G; Cappellini, Dm; Vasseur, C; Bursaux, E; Cutillo, S.
Hereditary spherocytosis: from clinical to molecular defects 1-gen-1998 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Alloisio, N; Morlé, L; Delaunay, J.
Hypercoagulability and atherothrombosis: Clinical suggestions and perspectives 1-gen-2001 Tufano, Antonella; Coppola, Antonio; Loffredo, Francesco; Garofano, Tiziana; Celentano, Aldo; Di Minno, Giovanni
Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis 1-gen-1997 Olivieri, O; DE FRANCESCHI, L; Bordin, L; Manfredi, M; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; DE VIVO, M; Guarini, P; Corrocher, R.
INFLUENZA DELLA BETA-ENDORFINA E DEL NALOXONE SULL’AGGREGAZIONE PIASTRINICA 1-gen-1993 A., Tirelli; G., Verrazzo; Giunta, Riccardo; A., Grassia; L., Coppola
The interactome of the N-terminus of band 3 regulates red blood cell metabolism and storage quality 1-gen-2021 Issaian, A.; Hay, A.; Dzieciatkowska, M.; Roberti, D.; Perrotta, S.; Darula, Z.; Redzic, J.; Busch, M. P.; Page, G. P.; Rogers, S. C.; Doctor, A.; Hansen, K. C.; Eisenmesser, E. Z.; Zimring, J. C.; D'Alessandro, A.
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 1-gen-2014 Rossi, Francesca; Perrotta, Silverio; Bellini, Giulia; Luongo, Livio; Tortora, C; Siniscalco, D; Francese, M; Torella, Marco; Nobili, Bruno; Di Marzo, V; Maione, Sabatino
Isolated ocular relapse in childhood acute lymphoblastic leukemia during continuing complete remission 1-gen-1996 Curto, Ml; D'Angelo, P; Jankovic, M; Fugardi, Mg; Ziino, O; Casale, Fiorina
ITP-like syndrome in cancer patients. 1-gen-2010 Guastafierro, Salvatore; Ferrara, Mg; Sica, A; Falcone, U; Rotunno, R; Santangelo, S; Coppola, L; Lucivero, Giacomo
Kaposi's sarcoma as clinical manifestation of the acquired immunodeficiency syndrome in a hemophilic patient 1-gen-1989 DE BIASI, R; Miraglia, E; Mastrullo, L; Rocino, A; Pisani, M; Ruocco, Vincenzo
Long-term disease free survival in an AML relapsed patient treated with FLANG plus Valproate 1-gen-2008 Falcone, U; Carbone, A; Riccardi, C; Troiano, M; Sica, A; Celentano, M; Guastafierro, Salvatore
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 1-gen-2013 Casale, Maddalena; Citarella, S; Palmieri, F; Lo Mastro, M; Pugliese, U; Amendola, G; De Michele, E; Ragozzino, A; Tartaglione, I; Della Rocca, F; Nobili, Bruno; Perrotta, Silverio
Longitudinal Prospective MRI Study in Pediatric Patients With Thalassemia Major 1-gen-2017 Casale, Maddalena; Meloni, A.; Filosa, A.; Pistoia, L.; Sorrentino, F.; Quarta, A.; Carollo, A.; Cirotto, M. C.; Positano, V.; Grassedonio, E.; Missere, M.; Pepe, A.
Marriage and parenthood among subjects cured of childhood cancer:a report from the Italian AIEOP Off-Therapy Registry 1-gen-2011 Pivetta, E; Maule, Mm; Pisani, P; Zugna, D; Haupt, R; Jankovic, M; Aricò, M; Casale, Fiorina; Clerico, A; CORDERO DI MONTEZEMOLO, L; Kiren, V; Locatelli, F; Palumbo, G; Pession, A; Pillon, M; Santoro, N; Terenziani, M; Valsecchi, Mg; Dama, E; Magnani, C; Merletti, F; Pastore, G.
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantation 1-gen-2005 Perrotta, Silverio; Conte, Ml; LA MANNA, A; Indolfi, P; Rossi, Francesca; Locatelli, F; Nobili, Bruno
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship 1-gen-2010 Iolascon, A; Russo, R; Esposito, Mr; Asci, R; Piscopo, C; Perrotta, Silverio; FÉNÉANT THIBAULT, M; Garçon, L; Delaunay, J.
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 1-gen-2014 De Rocco, D; Bottega, R; Cappelli, E; Cavani, S; Criscuolo, M; Nicchia, E; Corsolini, F; Greco, C; Borriello, Adriana; Svahn, J; Pillon, M; Mecucci, C; Casazza, G; Verzegnassi, F; Cugno, C; Locasciulli, A; Farruggia, P; Longoni, D; Ramenghi, U; Barberi, W; Tucci, F; Perrotta, Silverio; Grammatico, P; Hanenberg, H; DELLA RAGIONE, Fulvio; Dufour, C; Savoia, A; Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco, Hematology
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 1-gen-2004 Campagnoli, Mf; Garelli, E; Quarello, P; Carando, A; Varotto, S; Nobili, Bruno; Longoni, D; Pecile, V; Zecca, M; Dufour, C; Ramenghi, U; Dianzan, I.
Molecular heterogeneity of hereditary elliptocytosis in Italy 1-gen-1994 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Sannino, E; DE ANGELIS, F; Nobili, Bruno; Iolascon, A.
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