IOLASCON, ACHILLE

IOLASCON, ACHILLE  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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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.
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.
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
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.
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anemia (CDA II) 1.1 Articolo in rivista 2001 Iolascon, Achille; Sabato, V; DE MATTIA, D; Locatelli, F.
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
Incidence and outcome of hospital acquired malnutrition in children. 1.1 Articolo in rivista 2003 Campanozzi, A; Tummolo, A; Rutigliano, I; Nigro, A; Alberghini, V; D'Ademo, D; Romondia, A; Iolascon, Achille
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 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
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
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
Inherited thrombocytopenias: from genes to therapy 1.1 Articolo in rivista 2002 Balduini, C; Iolascon, Achille; Savoia, A.
Red blood cell membrane defects Rev. 1.1 Articolo in rivista 2003 Iolascon, Achille; PERROTTA S., AND GW STEWART
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.
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
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
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