IOLASCON, ACHILLE
IOLASCON, ACHILLE
Analysis of CDKN2A, CDKN2B, CDKN2C and Cyclin Ds gene status in hepatoblastoma.
1998-01-01 Iolascon, Achille; L., Giordani; A., Moretti; G., Basso; A., Borriello
Anemia diseritopoietica congenitas
2003-01-01 Iolascon, Achille
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genes.
2003-01-01 Giordani, L; Bruzzi, P; Lasalandra, C; Quaranta, M; Schittulli, F; DELLA RAGIONE, F; Iolascon, Achille
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anemia (CDA II)
2001-01-01 Iolascon, Achille; Sabato, V; DE MATTIA, D; Locatelli, F.
Caspase 3 and 8 deficiency in human neuroblastoma.
2003-01-01 Iolascon, Achille; Borriello, A; Giordani, L; Cucciolla, V; Moretti, A; Monno, F; Criniti, V; Marzullo, A; Criscuolo, M; Ragione, F. D.
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.
2003-01-01 Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, S; Lasalandra, C; Gasparini, P; Iolascon, Achille; Carella, M.
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
2002-01-01 Gigante, M; Monno, F; Roberto, R; Laforgia, N; Assael, Mb; Livolti, S; Caringella, A; LA MANNA, A; Masella, L; Iolascon, Achille
Erythroid membrane proteomic
2005-01-01 Orrù, S.; Caterino, M.; Ruoppolo, M.; Savoia, M.; Perrotta, S.; Salvatore, F.; Iolascon, Achille
Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)
2000-01-01 Perrotta, S; DEL GIUDICE, Em; Carbone, R; Servedio, V; SCHETTINI F., Jr; Nobili, B; Iolascon, Achille
Glucose-6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.
1994-01-01 F., Alfinito; V., Calabrò; M., Cappellini; G., Fiorelli; S., Filosa; Iolascon, Achille; E., MIRAGLIA DEL GIUDICE; S., Perrotta; R., Migliorati; D., Vallone; B., Rotoli; L., Luzzatto
Incidence and outcome of hospital acquired malnutrition in children.
2003-01-01 Campanozzi, A; Tummolo, A; Rutigliano, I; Nigro, A; Alberghini, V; D'Ademo, D; Romondia, A; Iolascon, A
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition
2002-01-01 Perrotta, S.; Nobili, B; Rossi, F; Criscuolo, M; Iolascon, Achille; DI PINTO, D; Pesaro, I; Cennamo, L; Oliva, A; DELLA RAGIONE, F.
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine
2003-01-01 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.
Localization of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11-q13
2000-01-01 Cusano, R; Gangarossa, S; Forabosco, P; Caridi, G; Ghiggeri, Gm; Russo, G; Iolascon, Achille; Ravazzolo, R; Seri, M.
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
2005-01-01 Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
2000-01-01 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.
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.
2003-01-01 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.
Natural history of congenital dyserythropoietic anemia type II (CDA II)
2001-01-01 Iolascon, Achille; Delaunay, J; Wickramasinghe, S; Perrotta, S; Gigante, M; A., Iolascon
Neonatal hyperbilirubinemia and Gilbert's syndrome.
2002-01-01 Laforgia, N; Faienza, Mf; Rinaldi, A; D'Amato, G; Rinaldi, G; Iolascon, Achille
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development.
1999-01-01 C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Analysis of CDKN2A, CDKN2B, CDKN2C and Cyclin Ds gene status in hepatoblastoma. | 1-gen-1998 | Iolascon, Achille; L., Giordani; A., Moretti; G., Basso; A., Borriello | |
| Anemia diseritopoietica congenitas | 1-gen-2003 | Iolascon, Achille | |
| Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genes. | 1-gen-2003 | Giordani, L; Bruzzi, P; Lasalandra, C; Quaranta, M; Schittulli, F; DELLA RAGIONE, F; Iolascon, Achille | |
| Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anemia (CDA II) | 1-gen-2001 | Iolascon, Achille; Sabato, V; DE MATTIA, D; Locatelli, F. | |
| Caspase 3 and 8 deficiency in human neuroblastoma. | 1-gen-2003 | Iolascon, Achille; Borriello, A; Giordani, L; Cucciolla, V; Moretti, A; Monno, F; Criniti, V; Marzullo, A; Criscuolo, M; Ragione, F. D. | |
| Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes. | 1-gen-2003 | Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, S; Lasalandra, C; Gasparini, P; Iolascon, Achille; Carella, M. | |
| Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. | 1-gen-2002 | Gigante, M; Monno, F; Roberto, R; Laforgia, N; Assael, Mb; Livolti, S; Caringella, A; LA MANNA, A; Masella, L; Iolascon, Achille | |
| Erythroid membrane proteomic | 1-gen-2005 | Orrù, S.; Caterino, M.; Ruoppolo, M.; Savoia, M.; Perrotta, S.; Salvatore, F.; Iolascon, Achille | |
| Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) | 1-gen-2000 | Perrotta, S; DEL GIUDICE, Em; Carbone, R; Servedio, V; SCHETTINI F., Jr; Nobili, B; Iolascon, Achille | |
| Glucose-6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia. | 1-gen-1994 | F., Alfinito; V., Calabrò; M., Cappellini; G., Fiorelli; S., Filosa; Iolascon, Achille; E., MIRAGLIA DEL GIUDICE; S., Perrotta; R., Migliorati; D., Vallone; B., Rotoli; L., Luzzatto | |
| Incidence and outcome of hospital acquired malnutrition in children. | 1-gen-2003 | Campanozzi, A; Tummolo, A; Rutigliano, I; Nigro, A; Alberghini, V; D'Ademo, D; Romondia, A; Iolascon, A | |
| Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition | 1-gen-2002 | Perrotta, S.; Nobili, B; Rossi, F; Criscuolo, M; Iolascon, Achille; DI PINTO, D; Pesaro, I; Cennamo, L; Oliva, A; DELLA RAGIONE, F. | |
| Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine | 1-gen-2003 | Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A. | |
| Localization of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11-q13 | 1-gen-2000 | Cusano, R; Gangarossa, S; Forabosco, P; Caridi, G; Ghiggeri, Gm; Russo, G; Iolascon, Achille; Ravazzolo, R; Seri, M. | |
| Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. | 1-gen-2005 | Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw | |
| Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 1-gen-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. | |
| 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-gen-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. | |
| Natural history of congenital dyserythropoietic anemia type II (CDA II) | 1-gen-2001 | Iolascon, Achille; Delaunay, J; Wickramasinghe, S; Perrotta, S; Gigante, M; A., Iolascon | |
| Neonatal hyperbilirubinemia and Gilbert's syndrome. | 1-gen-2002 | Laforgia, N; Faienza, Mf; Rinaldi, A; D'Amato, G; Rinaldi, G; Iolascon, Achille | |
| Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development. | 1-gen-1999 | C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini |