IOLASCON, ACHILLE
IOLASCON, ACHILLE
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
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.
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
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
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.
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.
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.
Spina bifida and folate-related genes: a study of gene-gene interactions.
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
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.
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.
Neonatal hyperbilirubinemia and Gilbert's syndrome.
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.
2002 Gigante, M; Monno, F; Roberto, R; Laforgia, N; Assael, Mb; Livolti, S; Caringella, A; LA MANNA, A; Masella, L; Iolascon, Achille
Analysis of three genetic polymorphisms as risk factors for thrombosis
1999 Giordano, P; Micelli, M; Coppola, B; Trerotoli, P; De Lucia, D; Iolascon, Achille
New Insights on CDAs
2011 Iolascon, Achille
Editorial Board
2011 Iolascon, Achille
L'anemia diseritropoietica di tipo II (CDAII): il mistero svelato
2012 Iolascon, Achille
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development.
1999 C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini
N-ras Gene Activation In Neuroblastoma
1991 Iolascon, Achille; A., Lania; M., Badiali; A., Pession; P., Esposito; E. M., Delgiudice; S., Perrotta; G., Basso; G. P., Tonini; S., Cutillo
Congenital dyserythropoietic anemias: a still unsolved puzzle.
2000 Iolascon, Achille
Anemias and liver
2011 Iolascon, Achille
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| 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. | |
| 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 | |
| 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 | |
| New Insights on CDAs | 8.02 Comunicazioni a Convegni o Seminari | 2011 | Iolascon, Achille | |
| Editorial Board | 8.06 Partecip. Editorial Board di riviste scientifiche | 2011 | Iolascon, Achille | |
| L'anemia diseritropoietica di tipo II (CDAII): il mistero svelato | 8.02 Comunicazioni a Convegni o Seminari | 2012 | Iolascon, Achille | |
| Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development. | 1.1 Articolo in rivista | 1999 | C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini | |
| N-ras Gene Activation In Neuroblastoma | 1.1 Articolo in rivista | 1991 | Iolascon, Achille; A., Lania; M., Badiali; A., Pession; P., Esposito; E. M., Delgiudice; S., Perrotta; G., Basso; G. P., Tonini; S., Cutillo | |
| Congenital dyserythropoietic anemias: a still unsolved puzzle. | 1.1 Articolo in rivista | 2000 | Iolascon, Achille | |
| Anemias and liver | 8.02 Comunicazioni a Convegni o Seminari | 2011 | Iolascon, Achille |