IOLASCON, ACHILLE
IOLASCON, ACHILLE
Dipartimento di Medicina molecolare e Biotecnologie mediche
Erythroid membrane proteomic
2004 Ruoppolo, M.; Caterino, Marianna; Orrù, S.; Savoia, M.; Iolascon, A.; Salvatore, F.
Genetica dell'osteoporosi
2012 Iolascon, Achille
Red blood cell membrane defects.
2003 Iolascon, Achille; Perrotta, S; Stewart, G. W.
RECOMBINANT ERYTHROPOIETIN THERAPY AS AN ALTERNATIVE TO BLOOD TRANSFUSIONS IN INFANTS WITH HEREDITARY SPHEROCYTOSIS.
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.
Analysis of three genetic polymorphisms as risk factors for thrombosis
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
2000 Cusano, R; Gangarossa, S; Forabosco, P; Caridi, G; Ghiggeri, Gm; Russo, G; Iolascon, Achille; Ravazzolo, R; Seri, M.
Increased methyl esterification of membrane proteins in aged red-blood cells. Preferentialesterification of ankyrin and band-4.1 cytoskeletal proteins.
1983 Galletti, P; Ingrosso, D; Nappi, A; Gragnaniello, V; Iolascon, Achille; Pinto, L.
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors.
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.
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.
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)
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.
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
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
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
2002 Giordani, L; Iolascon, Achille; Servedio, V; Mazzocco, K; Longo, G; Tonini, Gp
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition
2002 Perrotta, S.; Nobili, B; Rossi, F; Criscuolo, M; Iolascon, Achille; DI PINTO, D; Pesaro, I; Cennamo, L; Oliva, A; DELLA RAGIONE, F.
Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis
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
2002 Borriello, A; Roberto, R; DELLA RAGIONE, F; Iolascon, Achille
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.
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.
2003 Perrotta, S; Luzzatto, L; Carella, M; Iolascon, Achille
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Erythroid membrane proteomic | 4.1 Articoli in Atti di convegno | 2004 | Ruoppolo, M.; Caterino, Marianna; Orrù, S.; Savoia, M.; Iolascon, A.; Salvatore, F. | |
| Genetica dell'osteoporosi | 8.02 Comunicazioni a Convegni o Seminari | 2012 | Iolascon, Achille | |
| Red blood cell membrane defects. | 1.1 Articolo in rivista | 2003 | Iolascon, Achille; Perrotta, S; Stewart, G. W. | |
| 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. | |
| 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. | |
| Increased methyl esterification of membrane proteins in aged red-blood cells. Preferentialesterification of ankyrin and band-4.1 cytoskeletal proteins. | 1.1 Articolo in rivista | 1983 | Galletti, P; Ingrosso, D; Nappi, A; Gragnaniello, V; Iolascon, Achille; Pinto, L. | |
| 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 | |
| Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition | 1.1 Articolo in rivista | 2002 | Perrotta, S.; Nobili, B; Rossi, F; Criscuolo, M; Iolascon, Achille; DI PINTO, D; Pesaro, I; Cennamo, L; Oliva, A; DELLA RAGIONE, F. | |
| 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 |