AAAAAA
Results: 1-25/26
Authors:
Celada, P
Perrotta, S
Citation: P. Celada et S. Perrotta, On the minimum problem for nonconvex, multiple integrals of product type, CALC VAR P, 12(4), 2001, pp. 371-398
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:
Nobili, B
Perrotta, S
Matarese, SMR
Conte, ML
del Giudice, EM
Citation: B. Nobili et al., Evaluation of body iron status in Italian carriers of beta-thalassemia trait, NUTR RES, 21(1-2), 2001, pp. 55-60
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:
Celada, P
Perrotta, S
Citation: P. Celada et S. Perrotta, Minimizing nonconvex, simple integrals of product type, J DIFF EQUA, 171(1), 2001, pp. 148-172
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:
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:
Celada, P
Perrotta, S
Citation: P. Celada et S. Perrotta, Vectorial Hamilton-Jacobi equations with rank one affine dependence on thegradient, NONLIN ANAL, 41(3-4), 2000, pp. 383-404
Authors:
Celada, P
Perrotta, S
Citation: P. Celada et S. Perrotta, Minimizing non-convex multiple integrals: a density result, P RS EDIN A, 130, 2000, pp. 721-741
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:
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
Faienza, MF
Giordani, L
Perrotta, S
Ruggiu, G
Meloni, GF
del Giudice, EM
Citation: A. Iolascon et al., Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome, EUR J HAEMA, 62(5), 1999, pp. 307-310
Authors:
Perrotta, S
Iolascon, A
Polito, R
d'Urzo, G
Conte, ML
del Giudice, EM
Citation: S. Perrotta et al., 4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis, HAEMATOLOG, 84(7), 1999, pp. 660-662
Authors:
Iolascon, A
Faienza, MF
Perrotta, S
Meloni, GF
Ruggiu, G
del Giudice, EM
Citation: A. Iolascon et al., Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates, HAEMATOLOG, 84(2), 1999, pp. 99-102
Authors:
Flores-Bazan, F
Perrotta, S
Citation: F. Flores-bazan et S. Perrotta, Nonconvex variational problems related to a hyperbolic equation, SIAM J CON, 37(6), 1999, pp. 1751-1766
Authors:
Iolascon, A
Perrotta, S
Amendola, G
Altomare, M
Bagnara, GP
Del Vecchio, ME
Savoia, A
Citation: A. Iolascon et al., Familial dominant thrombocytopenia: Clinical, biologic, and molecular studies, PEDIAT RES, 46(5), 1999, pp. 548-552
Authors:
del Giudice, EM
Perrotta, S
Carbone, MT
Calabro, C
Esposito, L
De Rosa, C
Saviano, A
Di Toro, R
Perrone, L
Citation: Em. Del Giudice et al., Evaluation of leptin protein levels in patients with Cooley's anaemia, BR J HAEM, 105(3), 1999, pp. 839-840
Authors:
del Giudice, EM
Perrotta, S
Nobili, B
Specchia, C
d'Urzo, G
Iolascon, A
Citation: Em. Del Giudice et al., Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis, BLOOD, 94(7), 1999, pp. 2259-2262
Authors:
Iolascon, A
Stewart, GW
Ajetunmobi, JF
Perrotta, S
Delaunay, J
Carella, M
Zelante, L
Gasparini, P
Citation: A. Iolascon et al., Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis), BLOOD, 93(9), 1999, pp. 3120-3123
Authors:
Perrotta, S
Polito, R
Conte, ML
Nobili, B
Cutillo, S
del Giudice, EM
Nigro, V
Iolascon, A
Amendola, G
Citation: S. Perrotta et al., Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: Band 3 Vesuvio, BLOOD, 93(6), 1999, pp. 2131-2132