IOLASCON, ACHILLE
IOLASCON, ACHILLE
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
P27KIP1 accumulation is associated with retinoic induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation
2000 A., Borriello; V., DELLA PIETRA; M., Criscuolo; A., Oliva; Iolascon, Achille
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
Limiti della diagnosi molecolare di deficit di 21 idrossilasi
2011 Iolascon, Achille
Editorial Board
2011 Iolascon, Achille
Fondazione Neuroblastoma
2011 Iolascon, Achille
New Insights on CDAs
2011 Iolascon, Achille
Editorial Board
2011 Iolascon, Achille
The Italian Pediatric Survey On Hereditary Spherocytosis
1995 L., Pinto; Iolascon, Achille; E. M., Delgiudice; S. M., R.; B., Nobili; S., Perrotta
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| P27KIP1 accumulation is associated with retinoic induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation | 1.1 Articolo in rivista | 2000 | A., Borriello; V., DELLA PIETRA; M., Criscuolo; A., Oliva; Iolascon, Achille | |
| 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 | |
| Limiti della diagnosi molecolare di deficit di 21 idrossilasi | 8.02 Comunicazioni a Convegni o Seminari | 2011 | Iolascon, Achille | |
| Editorial Board | 8.06 Partecip. Editorial Board di riviste scientifiche | 2011 | Iolascon, Achille | |
| Fondazione Neuroblastoma | 8.05 Partecip. Consigli Scientifici/Direttivi | 2011 | 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 | |
| The Italian Pediatric Survey On Hereditary Spherocytosis | 1.1 Articolo in rivista | 1995 | L., Pinto; Iolascon, Achille; E. M., Delgiudice; S. M., R.; B., Nobili; S., Perrotta |