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Results:
1-11
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Results: 11
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:
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:
Falciani, M
Rinaldi, B
D'Agostino, B
Mazzeo, F
Rossi, S
Nobili, B
Rossi, F
Filippelli, A
Citation: M. Falciani et al., Effects of nebivolol on human platelet aggregation, J CARDIO PH, 38(6), 2001, pp. 922-929
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:
Berrino, L
Oliva, P
Rossi, F
Palazzo, E
Nobili, B
Maione, S
Citation: L. Berrino et al., Interaction between metabotropic and NMDA glutamate receptors in the periaqueductal grey pain modulatory system, N-S ARCH PH, 364(5), 2001, pp. 437-443
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:
Zecca, M
De Stefano, P
Nobili, B
Locatelli, F
Citation: M. Zecca et al., Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anemia, BLOOD, 97(12), 2001, pp. 3995-3997
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:
Ramenghi, U
Garelli, E
Valtolina, S
Campagnoli, MF
Timeus, F
Crescenzio, N
Mair, M
Varotto, S
D'Avanzo, M
Nobili, B
Massolo, F
Mori, PG
Locatelli, F
Gustavsson, P
Dahl, N
Dianzani, I
Citation: U. Ramenghi et al., Diamond-Blackfan anaemia in the Italian population, BR J HAEM, 104(4), 1999, pp. 841-848
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:
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
Risultati:
1-11
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