Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia von D'APOLITO, Maria, MARRONE, Agnese, SERVEDIO, Veronica, VAJRO, Pietro, DE FALCO, Luigia, IOLASCON, Achille

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K-CL co-transport plays an important role in normal and β thalassemic erythropoiesis von DE FRANCESCHI, Lucia, RONZONI, Luisa, DOMENICA CAPPELLINI, Maria, CIMMINO, Flora, SICILIANO, Angela, ALPER, Seth L, SERVEDIO, Veronica, POZZOBON, Christian, IOLASCON, Achille

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Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2) von Iolascon, Achille, d'Apolito, Maria, Servedio, Veronica, Cimmino, Flora, Piga, Antonio, Camaschella, Clara

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Hereditary Thrombocytopenia due to Reduced Platelet Production Report on two Families and Mutational Screening of the Thrombopoietin Receptor Gene (c-mpl) von TONELLI, R, STRIPPOLI, P, BORGNA-PIGNATTI, C, ROSITO, P, PESSION, A, PAOLUCCI, G, BAGNARA, G. P, GROSSI, A, SAVOIA, A, IOLASCON, A, SAVINO, M, SOCCORSA TERIACA, M, SERVEDIO, V, MORFINI, M, ZELANTE, L

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Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation von Servedio, Veronica, d'Apolito, Maria, Maiorano, Nunzia, Minuti, Barbara, Torricelli, Francesca, Ronchi, Flavio, Zancan, Lucia, Perrotta, Silverio, Vajro, Pietro, Boschetto, Loredana, Iolascon, Achille

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Osteoporosis in β-thalassaemia major patients : analysis of the genetic background von PERROTTA, Silverio, CAPPELLINI, Maria Domenica, BERTOLDO, Francesco, SERVEDIO, Veronica, IOLASCON, Giovanni, D'AGRUMA, Leonardo, GASPARINI, Paolo, SICILIANI, Maria Carmen, IOLASCON, Achille

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Prospective screening by a panfungal polymerase chain reaction assay in patients at risk for fungal infections : implications for the management of febrile neutropenia von HEBART, Holger, LÖFFLER, Jürgen, KERN, Winfried V, KANZ, Lothar, EINSELE, Hermann, REITZE, Heike, ENGEL, Andreas, SCHUMACHER, Ulrike, KLINGEBIEL, Thomas, BADER, Peter, BÖHME, Angelika, MARTIN, Hans, BUNJES, Donald

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Effect of DMT1 Mutations at Birth and in the First Years of Life von Achille, Iolascon, Maria, d'Apolito, Veronica, Servedio, Luigia, De Falco, Antonio, Piga, Clara, Camaschella

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K-CL co-transport plays an important role in normal and {beta} thalassemic erythropoiesis von De Franceschi, Lucia, Ronzoni, Luisa, Cappellini, Maria Domenica, Cimmino, Flora, Siciliano, Angela, Alper, Seth L, Servedio, Veronica, Pozzobon, Christian, Iolascon, Achille

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Genes transcriptionally modulated by interferon α2a correlate with the cytokine activity von IOLASCON, Achille, VOLINIA, Stefano, INDACO, Stefania, DELLA RAGIONE, Fulvio, BORRIELLO, Adriana, GIORDANI, Lucia, MORETTI, Arcangela, SERVEDIO, Veronica, MAIORANO, Nunzia, CUCCIOLLA, Valeria, CRINITI, Vittoria, GASPARINI, Paolo

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Spectrum ofUGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation von Servedio, Veronica, d'Apolito, Maria, Maiorano, Nunzia, Minuti, Barbara, Torricelli, Francesca, Ronchi, Flavio, Zancan, Lucia, Perrotta, Silverio, Vajro, Pietro, Boschetto, Loredana, Iolascon, Achille

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Osteoporosis in (beta)-thalassaemia major patients: Analysis of the genetic background von Perrotta, Silverio, Cappellini, Maria Domenica, Bertoldo, Francesco, Servedio, Veronica

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Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) von Perrotta, Silverio, del Giudice, Miraglia, Carbone, Ruggiero, Servedio, Veronica, Schettini, Federico, Nobili, Bruno, Iolascon, Achille

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Geographic distribution of CDA-II: did a founder effect operate in Southern Italy? von Iolascon, A, Servedio, V, Carbone, R, Totaro, A, Carella, M, Perrotta, S, Wickramasinghe, SN, Delaunay, J, Heimpel, H, Gasparini, P

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Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activity von Iolascon, A, Volinia, S, Borriello, A, Giordani, L, Moretti, A, Servedio, V, Maiorano, N, Cucciolla, V, Criniti, V, Gasparini, P, Indaco, S, Della Ragione, F

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Osteoporosis in β‐thalassaemia major patients: analysis of the genetic background von Perrotta, Silverio, Cappellini, Maria Domenica, Bertoldo, Francesco, Servedio, Veronica, Iolascon, Giovanni, D'agruma, Leonardo, Gasparini, Paolo, Siciliani, Maria Carmen, Iolascon, Achille

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Hereditary Thrombocytopenia due to Reduced Platelet Production von Tonelli, Roberto, Strippoli, Pierluigi, Grossi, Alberto, Savoia, Anna, Iolascon, Achille, Savino, Maria, Teriaca, Maria Soccorsa, Servedio, Veronica, Morfini, Massimo, Zelante, Leopoldo, Borgna-Pignatti, Caterina, Rosito, Pasquale, Pession, Andrea, Paolucci, Guido, Bagnara, Gian Paolo

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Two regions of deletion in 9p22∼p24 in neuroblastoma are frequently observed in favorable tumors von Giordani, Lucia, Iolascon, Achille, Servedio, Veronica, Mazzocco, Katia, Longo, Luca, Tonini, Gian Paolo

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