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Titolo Data di pubblicazione Autore(i) File
Vitamin A and infancy. Biochemical, functional, and clinical aspects 1-gen-2003 Perrotta, Silverio; Nobili, Bruno; Rossi, Francesca; DI PINTO, D; Cucciolla, V; Borriello, Adriana; Oliva, Adriana; DELLA RAGIONE, Fulvio
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes 1-gen-2003 Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, Silverio; Lasalandra, C; Gasparini, P; Iolascon, A; Carella, M.
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation 1-gen-2005 Servedio, V; D'Apolito, M; Maiorano, N; Minuti, B; Torricelli, F; Ronchi, F; Zancan, L; Perrotta, Silverio; Vajro, P; Boschetto, L; Iolascon, A.
Inherited disorders of bilirubin metabolism 1-gen-2005 Rossi, Francesca; Francese, M; Iodice, Rm; Falcone, E; Vetrella, S; Punzo, F; De Vita, S; Perrotta, Silverio
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
Idiopathic and secondary osteoporosis in childhood 1-gen-2005 Rossi, Francesca; Perrotta, Silverio; Falcone, E; Gimigliano, Francesca; Iodice, M; Vetrella, S; Iolascon, Giovanni
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 1-gen-2005 Perrotta, Silverio; Borriello, Adriana; Scaloni, A; DE FRANCESCHI, L; Brunati, Am; Turrini, F; Nigro, Vincenzo; MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno; Conte, Ml; Rossi, Francesca; Iolascon, A; DONELLA DEANA, A; Zappia, V; Poggi, V; Anong, W; Low, P; Mohandas, N; DELLA RAGIONE, Fulvio
Gilbert syndrome as differential diagnosis of hyperbilirubinemia in acquired aplastic anemia 1-gen-2005 Svahn, J; Lanciotti, M; Dufour, C; Perrotta, Silverio; Nobili, Bruno
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 1-gen-2006 Cappellini, M.; Cohen, A.; Piga, A.; Bejaoui, M.; Perrotta, Silverio; Agaoglu, L.; Aydinok, Y.; Kattamis, A.; Kilinc, Y.; Porter, J.; Capra, M.; Galanello, R.; Fattoum, S.; Drelichman, G.; Magnano, C.; Verissimo, M.; ATHANASSIOU METAXA, M.; Giardina, P.; KOURAKLI SYMEONIDIS, A.; JANKA SCHAUB, G.; Coates, T.; Vermylen, C.; Ollivieri, N.; Thuret, I.; Opitz, H.; RESSAYRE DJAFFER, C.; Marks, P.; Alberti, D.
Characterization of red cell membrane proteins as a function of red cell density: Annexin VII in different forms of hereditary spherocytosis 1-gen-2006 Caterino, M; Ruoppolo, M; Orru, S; Savoia, M; Perrotta, Silverio; Vecchio, Ld; Salvatore, F; Stewart, Gw; Iolascon, A.
Hepatitis C virus carriers with persistently normal ALT levels: biological peculiarities and update of the natural history of liver disease at 10 years 1-gen-2006 Persico, M; Perrotta, Silverio; Persico, E; Terracciano, L; Folgori, A; Ruggeri, L; Nicosia, A; Vecchione, R; Mura, Vl; Masarone, M; Torella, R.
Splenectomy in children with chronic ITP: long-term efficacy and relation between its outcome and responses to previous treatments 1-gen-2006 Ramenghi, U; Amendola, G; Farinasso, L; Giordano, P; Loffredo, G; Nobili, Bruno; Perrotta, Silverio; Russo, G; Zecca, M.
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 1-gen-2006 Perrotta, Silverio; Nobili, Bruno; Ferraro, M.; Migliaccio, C.; Borriello, Adriana; Cucciolla, V.; Martinelli, V.; Rossi, Francesca; Punzo, F.; Cirillo, P.; Parisi, G.; Zappia, V.; Rotoli, B.; DELLA RAGIONE, Fulvio
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 1-gen-2006 Parodi, E; Nobili, Bruno; Perrotta, Silverio; ROSARIA MATARESE, Sm; Russo, G; Licciardello, M; Zecca, M; Locatelli, F; Cesaro, S; Bisogno, G; Giordano, P; DE MATTIA, D; Ramenghia, U.
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.
Erythropoietin receptors on cancer cells: a still open question. 1-gen-2007 DELLA RAGIONE, Fulvio; Cucciolla, V.; Borriello, Adriana; Oliva, Adriana; Perrotta, Silverio
Renal hypoplasia without optic coloboma associated with PAX2 gene deletion 1-gen-2007 Benetti, E; Artifoni, L; Salviati, L; Pinello, L; Perrotta, Silverio; Zuffardi, O; Zacchello, G; Murer, L.
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 1-gen-2008 Conte, Ml; BERTOLI AVELLA, Am; DE GRAAF, Bm; Punzo, F; Lama, G; LA MANNA, A; Grassia, C; Rambaldi, Pier Francesco; Oostra, Ba; Perrotta, Silverio
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis 1-gen-2008 Amendola, G; DI CONCILIO, R; D'Urzo, G; Danise, P; Parisi, G; DELLA RAGIONE, Fulvio; Rossi, Francesca; Nobili, Bruno; Perrotta, Silverio
Hereditary spherocytosis. 1-gen-2008 Perrotta, Silverio; Gallagher, P. G.; Mohandas, N.
Mostrati risultati da 81 a 100 di 267
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