IRIS

IOLASCON, ACHILLE

IOLASCON, ACHILLE  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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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
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
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.
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.
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.
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.
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.
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.
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
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
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. 1.1 Articolo in rivista 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.
Congenital Dyserythropoietic Anemia type I is caused by mutations in codanin-1 1.1 Articolo in rivista 2002 Dgany, O; Avidan, N; Delaunay, J; Krasnov, T; Shalmon, L; Shalev, H; Markus, T; Cattan, D; Shishmanof, O; Iolascon, Achille; Beckann, S; Tamary, H.
Inherited thrombocytopenias: from genes to therapy 1.1 Articolo in rivista 2002 Balduini, C; Iolascon, Achille; Savoia, A.
RECOMBINANT ERYTHROPOIETIN THERAPY AS AN ALTERNATIVE TO BLOOD TRANSFUSIONS IN INFANTS WITH HEREDITARY SPHEROCYTOSIS. 1.1 Articolo in rivista 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, A. N. E. M. I. A. S.
Red blood cell membrane defects. 1.1 Articolo in rivista 2003 Iolascon, Achille; Perrotta, S; Stewart, G. W.
Clinical and molecular evaluation of non-dominant hereditary spherocytosis. 1.1 Articolo in rivista 2000 Miraglia del Giudice, E; Nobili, B; Francese, M; D'Urso, L; Iolascon, Achille; Eber, S; Perrotta, S.
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.
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.
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