Authors:
Acquila, M
Bicocchi, MP
Mori, PG
Odino, S
Valetto, A
Bottini, F
Citation: M. Acquila et al., A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy, EUR J HAEMA, 65(1), 2000, pp. 80-81
Authors:
Pasino, M
Lanza, T
Marotta, F
Scarso, L
De Biasio, P
Amato, S
Corcione, A
Pistoia, V
Mori, PG
Citation: M. Pasino et al., Flow cytometric and functional characterization of AC133(+) cells from human umbilical cord blood, BR J HAEM, 108(4), 2000, pp. 793-800
Authors:
Freedman, MH
Bonilla, MA
Fier, C
Bolyard, AA
Scarlata, D
Boxer, LA
Brown, S
Cham, B
Kannourakis, G
Kinsey, SE
Mori, PG
Cottle, T
Welte, K
Dale, DC
Citation: Mh. Freedman et al., Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy, BLOOD, 96(2), 2000, pp. 429-436
Authors:
Acquila, M
Bicocchi, MP
Bottini, F
Caprino, D
Bonifacino, O
Mori, PG
Citation: M. Acquila et al., A rapid prenatal diagnosis of hemophilia A by DNA analysis on crude chorionic villus biopsy, HAEMATOLOG, 84(4), 1999, pp. 382-383
Authors:
Perutelli, P
Lerzo, F
Calza, G
Cevasco, M
Mori, PG
Citation: P. Perutelli et al., Abnormalities of plasma von Willebrand factor multimeric structure inducedby extracorporeal circulation, HAEMATOLOG, 84(3), 1999, pp. 287-288
Authors:
Mori, PG
Priolo, M
Lerone, M
Caroli, F
Cusano, R
Seri, M
Silengo, MC
Citation: Pg. Mori et al., Congenital hypoplastic anaemia in a patient with a new multiple congenitalanomalies-mental retardation syndrome, AM J MED G, 87(1), 1999, pp. 36-39
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