IRIS

IOLASCON, ACHILLE

IOLASCON, ACHILLE  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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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
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
Basi molecolari delle anemie microcitiche da difetti ereditari del metabolismo del ferro 8.07 Progetti di Ricerca Finanziati 2011 Iolascon, Achille
Anemia diseritopoietica congenitas 2.1 Contributo in volume (Capitolo o Saggio) 2003 Iolascon, Achille
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
Restriction fragment length polymorphism analysis reveals different allele frequency and a linkage disequilibrium at locus D1S94 in neuroblastoma patients 1.1 Articolo in rivista 1997 Perri, P; Pession, A; Mazzocco, K; Scaruffi, P; Strigini, P; Iolascon, Achille; Albergoni, Mp; Basso, G; Tonini, G. P.
Maple-syrup-urine-disease (msud) - Screening For Known Mutations In Italian Patients 1.1 Articolo in rivista 1994 T., Parrella; S., Surrey; Iolascon, Achille; M., Sartore; R., Heidenreich; G., Diamond; A., Ponzone; O., Guardamagna; A. B., Burlina; R., Cerone; R., Parini; C., Dionisivici; E., Rappaport; P., Fortina
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome. 1.1 Articolo in rivista 1999 Iolascon, Achille; Faienza, Mf; Giordani, L; Perrotta, S; Ruggiu, G; Meloni, Gf; del Giudice, E. M.