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Glucose-6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia. 1-gen-1994 F., Alfinito; V., Calabrò; M., Cappellini; G., Fiorelli; S., Filosa; Iolascon, Achille; E., MIRAGLIA DEL GIUDICE; S., Perrotta; R., Migliorati; D., Vallone; B., Rotoli; L., Luzzatto
Analysis of CDKN2A, CDKN2B, CDKN2C and Cyclin Ds gene status in hepatoblastoma. 1-gen-1998 Iolascon, Achille; L., Giordani; A., Moretti; G., Basso; A., Borriello
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development. 1-gen-1999 C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini
Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 1-gen-2000 Perrotta, S; DEL GIUDICE, Em; Carbone, R; Servedio, V; SCHETTINI F., Jr; Nobili, B; Iolascon, Achille
P27KIP1 accumulation is associated with retinoic induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation 1-gen-2000 A., Borriello; V., DELLA PIETRA; M., Criscuolo; A., Oliva; Iolascon, Achille
Localization of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11-q13 1-gen-2000 Cusano, R; Gangarossa, S; Forabosco, P; Caridi, G; Ghiggeri, Gm; Russo, G; Iolascon, Achille; Ravazzolo, R; Seri, M.
Osteoporosis in b-thalassaemia major patients: analysis of the genetic background 1-gen-2000 Perrotta, S; Cappellini, Md; Bertoldo, F; Servedio, V; Iolascon, G; D'Agruma, L; Gasparini, P; Siciliani, Mc; Iolascon, Achille
RECOMBINANT ERYTHROPOIETIN THERAPY AS AN ALTERNATIVE TO BLOOD TRANSFUSIONS IN INFANTS WITH HEREDITARY SPHEROCYTOSIS. 1-gen-2000 Tchernia, G; Delhommeau, F; Perrotta, S; Cynober, T; BADER MEUNIER, B; Nobili, B; Rohrlich, P; Salomon, Jl; SAGOT BEVENOT, S; DEL GIUDICE, Em; Delaunay, J; Demattia, D; Schischmanoff, Po; Mohandas, N; Iolascon, Achille; ESPHI WORKING GROUP ON HEMOLYTIC, Anemias
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. 1-gen-2000 Seri, M; Cusano, R; Gangarossa, S; Caridi, G; Bordo, D; LO NIGRO, C; Ghiggeri, Gm; Ravazzolo, R; Savino, M; DEL VECCHIO, M; D'Apolito, M; Iolascon, Achille; Zelante, Ll; Savoia, A; Balduini, Cl; Noris, P; Magrini, U; Belletti, S; Heath, Ke; Babcock, M; Glucksman, Mj; Aliprandis, E; Bizzaro, N; Desnick, Rj; Martignetti, J. A.
Reduced Expression of Transforming Growth Factor-Beta Receptor Type III in High Stages Neuroblastoma. 1-gen-2000 Iolascon, Achille; Giordani, L; Borriello, A; Carbone, R; Izzo, A; Tonini, Gp; Gambini, C; DELLA RAGIONE, F.
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors. 1-gen-2001 Iolascon, Achille; Giordano, P; Storelli, S; Li, Hh; Coppola, B; Piga, A; Fantola, E; Forni, G; Cianciulli, P; Perrotta, S; Magnano, C; Maggio, A; Mangiagli, A; Devoto, M.
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anemia (CDA II) 1-gen-2001 Iolascon, Achille; Sabato, V; DE MATTIA, D; Locatelli, F.
Natural history of congenital dyserythropoietic anemia type II (CDA II) 1-gen-2001 Iolascon, Achille; Delaunay, J; Wickramasinghe, S; Perrotta, S; Gigante, M; A., Iolascon
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 1-gen-2002 Perrotta, S.; Nobili, B; Rossi, F; Criscuolo, M; Iolascon, Achille; DI PINTO, D; Pesaro, I; Cennamo, L; Oliva, A; DELLA RAGIONE, F.
Neonatal hyperbilirubinemia and Gilbert's syndrome. 1-gen-2002 Laforgia, N; Faienza, Mf; Rinaldi, A; D'Amato, G; Rinaldi, G; Iolascon, Achille
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. 1-gen-2002 Gigante, M; Monno, F; Roberto, R; Laforgia, N; Assael, Mb; Livolti, S; Caringella, A; LA MANNA, A; Masella, L; Iolascon, Achille
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genes. 1-gen-2003 Giordani, L; Bruzzi, P; Lasalandra, C; Quaranta, M; Schittulli, F; DELLA RAGIONE, F; Iolascon, Achille
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis. 1-gen-2003 Fricke, B; Argent, Ac; Chetty, Mc; Pizzey, Ar; Turner, Ej; Ho, Mm; Iolascon, Achille; VON DURING, M; Stewart, G. W.
Caspase 3 and 8 deficiency in human neuroblastoma. 1-gen-2003 Iolascon, Achille; Borriello, A; Giordani, L; Cucciolla, V; Moretti, A; Monno, F; Criniti, V; Marzullo, A; Criscuolo, M; Ragione, F. D.
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. 1-gen-2003 Seri, M; Pecci, A; DI BARI, F; Cusano, R; Savino, M; Panza, E; Nigro, A; Noris, P; Gangarossa, S; Rocca, B; Gresele, P; Bizzaro, N; Malatesta, P; Koivisto, Pa; Longo, I; Musso, R; Pecoraro, C; Iolascon, Achille; Magrini, U; RODRIGUEZ SORIANO, J; Renieri, A; Ghiggeri, Gm; Ravazzolo, R; Balduini, Cl; Savoia, A.
Mostrati risultati da 1 a 20 di 28
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