IOLASCON, ACHILLE
IOLASCON, ACHILLE
Red blood cell membrane defects Rev.
2003 Iolascon, Achille; PERROTTA S., AND GW STEWART
Osteoporosis in b-thalassaemia major patients: analysis of the genetic background
2000 Perrotta, S; Cappellini, Md; Bertoldo, F; Servedio, V; Iolascon, G; D'Agruma, L; Gasparini, P; Siciliani, Mc; 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
Inherited thrombocytopenias: from genes to therapy
2002 Balduini, C; Iolascon, Achille; Savoia, A.
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
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.
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.
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.
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.
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.
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.
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
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development.
1999 C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini
Proliferate and survive: cell division cycle and apoptosis in human neuroblastoma
2002 Borriello, A; Roberto, R; DELLA RAGIONE, F; Iolascon, Achille
Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
---|---|---|---|---|
Red blood cell membrane defects Rev. | 1.1 Articolo in rivista | 2003 | Iolascon, Achille; PERROTTA S., AND GW STEWART | |
Osteoporosis in b-thalassaemia major patients: analysis of the genetic background | 1.1 Articolo in rivista | 2000 | Perrotta, S; Cappellini, Md; Bertoldo, F; Servedio, V; Iolascon, G; D'Agruma, L; Gasparini, P; Siciliani, Mc; 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 | |
Inherited thrombocytopenias: from genes to therapy | 1.1 Articolo in rivista | 2002 | Balduini, C; Iolascon, Achille; Savoia, A. | |
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 | |
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. | |
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. | |
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. | |
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. | |
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. | |
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. | |
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 | |
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development. | 1.1 Articolo in rivista | 1999 | C., LO CONSULO; Iolascon, Achille; A., Cavazzana; R., Cusano; P., Strigini | |
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 |