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.
Reduced Expression of Transforming Growth Factor-Beta Receptor Type III in High Stages Neuroblastoma.
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
2003 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.
Hereditary stomatocytosis and other very rare membrane disorders
2012 Iolascon, Achille
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
1999 Iolascon, Achille; Faienza, Mf; Giordani, L; Perrotta, S; Ruggiu, G; Meloni, Gf; del Giudice, E. M.
Red blood cell membrane defects.
2003 Iolascon, Achille; Perrotta, S; Stewart, G. W.
Congenital Dyserythropoietic Anemia type I is caused by mutations in codanin-1
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.
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.
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
2002 Balduini, C; Iolascon, Achille; Savoia, A.
Clinical and molecular evaluation of non-dominant hereditary spherocytosis.
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.
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.
2003 Perrotta, S; Luzzatto, L; Carella, M; Iolascon, Achille
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.
2003 Fricke, B; Argent, Ac; Chetty, Mc; Pizzey, Ar; Turner, Ej; Ho, Mm; Iolascon, Achille; VON DURING, M; Stewart, G. W.
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.
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
Natural history of congenital dyserythropoietic anemia type II (CDA II)
2001 Iolascon, Achille; Delaunay, J; Wickramasinghe, S; Perrotta, S; Gigante, M; A., Iolascon
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
| 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. | |
| 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 | |
| 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 | |
| The "stomatin" gene and protein in overhydrated hereditary stomatocytosis. | 1.1 Articolo in rivista | 2003 | Fricke, B; Argent, Ac; Chetty, Mc; Pizzey, Ar; Turner, Ej; Ho, Mm; Iolascon, Achille; VON DURING, M; Stewart, G. W. | |
| 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. | |
| 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 | |
| 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 | |
| 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 |