IRIS

IOLASCON, ACHILLE

IOLASCON, ACHILLE  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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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.
Reduced Expression of Transforming Growth Factor-Beta Receptor Type III in High Stages Neuroblastoma. 1.1 Articolo in rivista 2000 Iolascon, Achille; Giordani, L; Borriello, A; Carbone, R; Izzo, A; Tonini, Gp; Gambini, C; DELLA RAGIONE, F.
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine 1.1 Articolo in rivista 2003 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.
Hereditary stomatocytosis and other very rare membrane disorders 8.02 Comunicazioni a Convegni o Seminari 2012 Iolascon, Achille
Erythroid membrane proteomic 4.1 Articoli in Atti di convegno 2004 Ruoppolo, M.; Caterino, Marianna; Orrù, S.; Savoia, M.; Iolascon, A.; Salvatore, F.
Loss of 10q26.1-q26.3 in association with 7q34-q36.3 gain or 17q24.3-q25.3 gain predict poor outcome in pediatric medulloblastoma. 1.1 Articolo in rivista 2011 Pezzolo, A; Coco, S; Raso, A; Parodi, F; Pistorio, A; Valdora, F; Capra, V; Zollo, Massimo; Aschero, S; Basso, E; Cama, A; Nozza, P; Gambini, C; Cinalli, G; Garrè, Ml; Iolascon, Achille; Pistoia, V; Tonini, G. P.
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. 1.1 Articolo in rivista 2011 Nguyen le, B; Diskin, Sj; Capasso, Mario; Wang, K; Diamond, Ma; Glessner, J; Kim, C; Attiyeh, Ef; Mosse, Yp; Cole, K; Iolascon, Achille; Devoto, M; Hakonarson, H; Li, Hk; Maris, J. M.
Retinoic acid induces P27(Kip1) nuclear accumulation by modulating its phosphorylation 1.1 Articolo in rivista 2006 A., Borriello; V., Cucciolla; M., Criscuolo; S., Indaco; A., Oliva; A., Giovane; D., Bencivenga; Iolascon, Achille; V., Zappia; F. D., Ragione
Age-dependent Prognostic-significance of N-myc Amplification In Neuroblastoma - the Italian Experience 1.1 Articolo in rivista 1991 R., Sansone; P., Strigini; M., Badiali; C., Dominici; V., Fontana; Iolascon, Achille; B., Debernardi; G. P., Tonini
Combinations of genetic data in a study of neuroblastoma risk genotypes 1.1 Articolo in rivista 2014 Capasso, Mario; Francesco Maria, Calabrese; Iolascon, Achille; Erling, Mellerup
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.
Red blood cell membrane defects. 1.1 Articolo in rivista 2003 Iolascon, Achille; Perrotta, S; Stewart, G. W.
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.
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.
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.
Inherited thrombocytopenias: from genes to therapy 1.1 Articolo in rivista 2002 Balduini, C; Iolascon, Achille; Savoia, A.
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.
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