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A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT) 1-gen-2017 Noris, P; Marconi, C; De Rocco, D; Melazzini, F; Pippucci, T; Loffredo, G; Giangregorio, T; Cigalini, E; Pecci, A; Seri, M; Savoia, A
Nodular lesions of the liver in multiple myeloma 1-gen-2007 Invernizzi, Rosangela; Carnevale Maffe, G; Travaglino, E; Pagani, E; Pieresca, C.
NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL 1-gen-2017 Zaninetti, C; De Rocco, D; Pastore, A; Bozzi, V; Barozzi, S; Melazzini, F; Savoia, A; Noris, P; Balduini, Cl; Pecci, A
NOVEL RUNX1 MUTATIONS IN FAMILIES WITH INHERITED THROMBOCYTOPENIA 1-gen-2017 Noris, P; De Rocco, D; Melazzini, F; Marconi, C; Pecci, A; Bottega, R; Gnan, C; Palombo, F; Giordano, P; Coccioli, Ms; Glembotsky, Ac; Cigalini, E; Heller, Pg; Seri, M; Savoia, A
Oral melphalan and dexamethasone grants extended survival with minimal toxicity in AL amyloidosis: long-term results of a risk-adapted approach 1-gen-2014 Palladini, Giovanni; Milani, P.; Foli, A.; Obici, L.; Lavatelli, Francesca; Nuvolone, MARIO ULISSE; Caccialanza, R.; Perlini, Stefano; Merlini, Giampaolo
PAS positive monocytes in Whipple s disease. 1-gen-2003 Invernizzi, Rosangela; E., Travaglino; V., Perfetti
Reduced intensity stem cell transplantation for advanced soft tissue sarcomas in adults: a retrospective analysis of the European Group for Blood and Marrow Transplantation 1-gen-2007 Secondino, Simona; Carrabba, Matteo G; Pedrazzoli, Paolo; Castagna, Luca; Spina, Francesco; Grosso, Federica; Bertuzzi, Alexia; Bay, Jacques-Olivier; Siena, Salvatore; Corradini, Paolo; Niederwieser, Dietger; Demirer, Taner
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy 1-gen-2021 Homan, Claire C; King-Smith, Sarah L; Lawrence, David M; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W; Yu, Kai; Bödör, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D; Duployez, Nicolas; Favier, Remi; Fröhling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M; Krämer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A; Schreiber, Andreas W; Hahn, Christopher N; Scott, Hamish S; Brown, Anna L
Treating advanced cardiac damage in light chain amyloidosis: still an unmet need 1-gen-2014 Merlini, Giampaolo; Palladini, Giovanni
Update on treatment of light chain amyloidosis 1-gen-2014 S., Mahmood; Palladini, Giovanni; V., Sanchorawala; A., Wechalekar
VEGF-induced Ca2+signals are deranged in endothelial progenitor cells from patients with myelofibrosis carrying JAK2 mutations 1-gen-2014 Dragoni, Silvia; Poletto, V.; Ruffinatti, F. A.; Barosi, G.; Tanzi, Franco; Rosti, V.; Moccia, Francesco
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