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Results: 1-25/41
Authors:
Perrotta, S
del Giudice, EM
Iolascon, A
De Vivo, M
Di Pinto, D
Cutillo, S
Nobili, B
Citation: S. Perrotta et al., Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia, LEUKEMIA, 15(3), 2001, pp. 440-444
Authors:
Iolascon, A
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
Citation: A. Iolascon et al., Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors, HAEMATOLOG, 86(10), 2001, pp. 1112-1113
Authors:
Giordano, P
Laforgia, N
Di Giulio, G
Storelli, S
Mautone, A
Iolascon, A
Citation: P. Giordano et al., Renal vein thrombosis in a newborn with prothrombotic genetic risk factors, J PERIN MED, 29(2), 2001, pp. 163-166
Authors:
Iolascon, A
Sabato, V
de Mattia, D
Locatelli, F
Citation: A. Iolascon et al., Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II), BONE MAR TR, 27(2), 2001, pp. 213-215
Authors:
Danise, P
Amendola, G
Nobili, B
Perrotta, S
Del Giudice, EM
Matarese, SMR
Iolascon, A
Brugnara, C
Citation: P. Danise et al., Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis, CLIN LAB H, 23(1), 2001, pp. 7-13
Authors:
del Giudice, EM
Nobili, B
Francese, M
D'Urso, L
Iolascon, A
Eber, S
Perrotta, S
Citation: Em. Del Giudice et al., Clinical and molecular evaluation of non-dominant hereditary spherocytosis, BR J HAEM, 112(1), 2001, pp. 42-47
Authors:
Iolascon, A
Delaunay, J
Wickramasinghe, SN
Perrotta, S
Gigante, M
Camaschella, C
Citation: A. Iolascon et al., Natural history of congenital dyserythropoietic anemia type II, BLOOD, 98(4), 2001, pp. 1258-1260
Authors:
Savoia, A
Balduini, CL
Savino, M
Noris, P
Del Vecchio, M
Perrotta, S
Belletti, S
Poggi, V
Iolascon, A
Citation: A. Savoia et al., Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome, BLOOD, 97(5), 2001, pp. 1330-1335
Authors:
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, A
Zelante, LL
Savoia, A
Balduini, CL
Noris, P
Magrini, U
Belletti, S
Citation: M. Seri et al., Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes, NAT GENET, 26(1), 2000, pp. 103-105
Authors:
Cusano, R
Gangarossa, S
Forabosco, P
Caridi, G
Ghiggeri, GM
Russo, G
Iolascon, A
Ravazzolo, R
Seri, M
Citation: R. Cusano et al., Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13, EUR J HUM G, 8(11), 2000, pp. 895-899
Authors:
Borriello, A
Della Pietra, V
Criscuolo, M
Oliva, A
Tonini, GP
Iolascon, A
Zappia, V
Della Ragione, F
Citation: A. Borriello et al., p27(Kip1) accumulation is associated with retinoic-induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation, ONCOGENE, 19(1), 2000, pp. 51-60
Authors:
Iolascon, A
Martire, B
Lee, MJ
Wickramasinghe, SN
Citation: A. Iolascon et al., Transfusion-dependent congenital dyserythropoietic anaemia with intraerythroblastic inclusions of a non-globin protein, EUR J HAEMA, 65(2), 2000, pp. 140-143
Authors:
Giordano, P
Del Vecchio, GC
Santoro, N
Arcamone, G
Coppola, B
Altomare, M
Schettini, F
Iolascon, A
De Mattia, D
Citation: P. Giordano et al., Thrombin generation in children with acute lymphoblastic leukemia: Effect of leukemia immunophenotypic subgroups, PED HEM ONC, 17(8), 2000, pp. 667-672
Authors:
Bertoldo, F
D'Agruma, L
Furlan, F
Colapietro, F
Lorenzi, MT
Maioran, N
Iolascon, A
Zelante, L
Locascio, V
Gasparini, P
Citation: F. Bertoldo et al., Transforming growth factor-beta 1 gene polymorphism, bone turnover, and bone mass in Italian postmenopausal women, J BONE MIN, 15(4), 2000, pp. 634-639
Authors:
Iolascon, A
Citation: A. Iolascon, Congenital dyserythropoietic anemias: a still unsolved puzzle, HAEMATOLOG, 85(7), 2000, pp. 673-674
Authors:
Iolascon, A
Servedio, V
Carbone, R
Totaro, A
Carella, M
Perrotta, S
Wickramasinghe, SN
Delaunay, J
Heimpel, H
Gasparini, P
Citation: A. Iolascon et al., Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?, HAEMATOLOG, 85(5), 2000, pp. 470-474
Authors:
Iolascon, A
Perrotta, S
Coppola, B
Carbone, R
del Giudice, EM
Citation: A. Iolascon et al., Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphismin Southern Italy, HAEMATOLOG, 85(3), 2000, pp. 335-336
Authors:
Beauchamp-Nicoud, A
Morle, L
Lutz, HU
Stammler, P
Agulles, O
Petermann-Khder, R
Iolascon, A
Perrotta, S
Cynober, T
Tchernia, G
Delaunay, J
Baudin-Creuza, V
Citation: A. Beauchamp-nicoud et al., Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG), HAEMATOLOG, 85(1), 2000, pp. 19-24
Authors:
Tonelli, R
Strippoli, P
Grossi, A
Savoia, A
Iolascon, A
Savino, M
Teriaca, MS
Servedio, V
Morfini, M
Zelante, L
Borgna-Pignatti, C
Rosito, P
Pession, A
Paolucci, G
Bagnara, GP
Citation: R. Tonelli et al., Hereditary thrombocytopenia due to reduced platelet production - Report ontwo families and mutational screening of the thrombopoietin receptor gene (c-mpl), THROMB HAEM, 83(6), 2000, pp. 931-936
Authors:
Perrotta, S
del Giudice, EM
Carbone, R
Servedio, V
Schettini, F
Nobili, B
Iolascon, A
Citation: S. Perrotta et al., Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II), J PEDIAT, 136(4), 2000, pp. 556-559
Authors:
Iolascon, A
Meloni, A
Coppola, B
Rosatelli, MC
Citation: A. Iolascon et al., Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5 '-diphosphate-glucuronosyltransferase (UGT1A1) gene, J MED GENET, 37(9), 2000, pp. 712-713
Authors:
Perrotta, S
Cappellini, MD
Bertoldo, F
Servedio, V
Iolascon, G
D'Agruma, L
Gasparini, P
Siciliani, MC
Iolascon, A
Citation: S. Perrotta et al., Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background, BR J HAEM, 111(2), 2000, pp. 461-466
Authors:
Iolascon, A
Giordani, L
Borriello, A
Carbone, R
Izzo, A
Tonini, GP
Gambini, C
Della Ragione, F
Citation: A. Iolascon et al., Reduced expression of transforming growth factor-beta receptor type III inhigh stage neuroblastomas, BR J CANC, 82(6), 2000, pp. 1171-1176
Authors:
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, A
Delaunay, J
Citation: S. Grootenboer et al., Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24, BLOOD, 96(7), 2000, pp. 2599-2605
Authors:
Delaunay, J
Iolascon, A
Citation: J. Delaunay et A. Iolascon, The congenital dyserythropoietic anaemias, BEST P R C, 12(4), 1999, pp. 691-705