IOLASCON, ACHILLE

IOLASCON, ACHILLE  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Analysis of three genetic polymorphisms as risk factors for thrombosis 1.1 Articolo in rivista 1999 Giordano, P; Micelli, M; Coppola, B; Trerotoli, P; De Lucia, D; Iolascon, Achille
Localization of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11-q13 1.1 Articolo in rivista 2000 Cusano, R; Gangarossa, S; Forabosco, P; Caridi, G; Ghiggeri, Gm; Russo, G; Iolascon, Achille; Ravazzolo, R; Seri, M.
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors. 1.1 Articolo in rivista 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.
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. 1.1 Articolo in rivista 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.
Neonatal hyperbilirubinemia and Gilbert's syndrome. 1.1 Articolo in rivista 2002 Laforgia, N; Faienza, Mf; Rinaldi, A; D'Amato, G; Rinaldi, G; Iolascon, Achille
Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 1.1 Articolo in rivista 2000 Perrotta, S; DEL GIUDICE, Em; Carbone, R; Servedio, V; SCHETTINI F., Jr; Nobili, B; Iolascon, Achille
Structural and functional analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B and CDKN2C) in neuroblastoma. 1.1 Articolo in rivista 1998 Iolascon, Achille; L., Giordani; A., Moretti; G. P., Tonini; C., LO CUNSOLO
Spina bifida and folate-related genes: a study of gene-gene interactions 1.1 Articolo in rivista 2002 DE FRANCHIS, L; Botto, R; Sebastio, G; Ricci, R; Iolascon, Achille; Capra, V; Andria, G; Mastroiacovo, P.
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24 1.1 Articolo in rivista 2000 Grootenboer, S; Schischmanoff, Po; Laurendeau, I; Cynober, T; Tchernia, G; Dommergues, Jp; Dhermy, D; Bost, M; Varet, B; Snyder, M; Ballas, Sk; Ducot, B; Babron, Mc; Stewart, Gw; Gasparini, P; Iolascon, Achille; Delaunay, J.
Two regions of deletion 9p22-p24 in neuroblastoma are frequently observed in favorable tumors 1.1 Articolo in rivista 2002 Giordani, L; Iolascon, Achille; Servedio, V; Mazzocco, K; Longo, G; Tonini, Gp
Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis 1.1 Articolo in rivista 2002 Reliene, R; Mariani, M; Zanella, A; Rehinhart, O; Ribeiro, Ml; Miraglia, E; Perrotta, S; Iolascon, Achille; Lutz, H.
Proliferate and survive: cell division cycle and apoptosis in human neuroblastoma 1.1 Articolo in rivista 2002 Borriello, A; Roberto, R; DELLA RAGIONE, F; Iolascon, Achille
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes. 1.1 Articolo in rivista 2003 Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, S; Lasalandra, C; Gasparini, P; Iolascon, Achille; Carella, M.
Congenital dyserythropoietic anemia type II in human patients is not due to mutations in the erythroid anion exchanger 1. 1.1 Articolo in rivista 2003 Perrotta, S; Luzzatto, L; Carella, M; Iolascon, Achille
Spina bifida and folate-related genes: a study of gene-gene interactions. 1.1 Articolo in rivista 2002 DE FRANCHIS, R; Botto, Ld; Sebastio, G; Ricci, R; Iolascon, Achille; Capra, V; Andria, G; Mastroiacovo, P.
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis. 1.1 Articolo in rivista 2003 Fricke, B; Argent, Ac; Chetty, Mc; Pizzey, Ar; Turner, Ej; Ho, Mm; Iolascon, Achille; VON DURING, M; Stewart, G. W.
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. 1.1 Articolo in rivista 2002 Gigante, M; Monno, F; Roberto, R; Laforgia, N; Assael, Mb; Livolti, S; Caringella, A; LA MANNA, A; Masella, L; Iolascon, Achille
Characterization of the CYP21 gene 5' flanking region in patients affected by 21-OH deficiency 1.1 Articolo in rivista 2000 Bobba, A; Marra, E; Lattanzio, P; Iolascon, Achille; Giannattasio, S.
Natural history of congenital dyserythropoietic anemia type II (CDA II) 1.1 Articolo in rivista 2001 Iolascon, Achille; Delaunay, J; Wickramasinghe, S; Perrotta, S; Gigante, M; A., Iolascon
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine 1.1 Articolo in rivista 2003 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.