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F Rodeghiero

Showing results (181-190 of 266) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|April 20, 2010
F8 mRNA studies in haemophilia A patients with different splice site mutationsG Castaman, S H Giacomelli, M E Mancuso, et al.
American Journal of Hematology|November 17, 2006
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: definite evidence for the non-penetrance of the C2362F mutationG Castaman, K Bertoncello, M Bernardi, et al.
Minerva Stomatologica|March 7, 1998
[Prevention of hemorrhage and dental treatment of patients with congenital or acquired coagulopathies]R Vangelisti, O Pagnacco, G Ristagno, et al.
Transfusion|September 1, 1992
Fibrin glue from single-donation autologous plasmapheresisB Casali, F Rodeghiero, A Tosetto, et al.
Haematologica|November 1, 1993
Hematologic and cytogenetic analyses of 99 cases of de novo myelodysplastic syndromesA D'Emilio, A Montaldi, M Stella, et al.
Bone Marrow Transplantation|July 6, 2004
ABO-incompatible bone marrow transplantation: a GITMO survey of current practice in Italy and comparison with the literatureR Raimondi, M Soli, T Lamparelli, et al.
Blood|April 1, 1996
Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domainT Izumi, T Hashiguchi, G Castaman, et al.
Dental Cadmos|January 31, 1987
[Tooth extractions in patients with hemophilia and von Willebrand's disease]R Vangelisti, D N Rositani, A Pagnacco, et al.
Blood|April 1, 1984
Liver dysfunction rather than intravascular coagulation as the main cause of low protein C and antithrombin III in acute leukemiaF Rodeghiero, P M Mannucci, S Viganò, et al.
British Journal of Haematology|December 1, 1996
A (15;17) translocation not associated with acute promyelocytic leukaemiaE Di Bona, A Montaldi, N Guercini, et al.
Pageof 27

Showing results (181-190 of 266) with videos related to

Sort By:
Pageof 27
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 20, 2010
F8 mRNA studies in haemophilia A patients with different splice site mutationsG Castaman, S H Giacomelli, M E Mancuso, et al.
American Journal of Hematology|November 17, 2006
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: definite evidence for the non-penetrance of the C2362F mutationG Castaman, K Bertoncello, M Bernardi, et al.
Minerva Stomatologica|March 7, 1998
[Prevention of hemorrhage and dental treatment of patients with congenital or acquired coagulopathies]R Vangelisti, O Pagnacco, G Ristagno, et al.
Transfusion|September 1, 1992
Fibrin glue from single-donation autologous plasmapheresisB Casali, F Rodeghiero, A Tosetto, et al.
Haematologica|November 1, 1993
Hematologic and cytogenetic analyses of 99 cases of de novo myelodysplastic syndromesA D'Emilio, A Montaldi, M Stella, et al.
Bone Marrow Transplantation|July 6, 2004
ABO-incompatible bone marrow transplantation: a GITMO survey of current practice in Italy and comparison with the literatureR Raimondi, M Soli, T Lamparelli, et al.
Blood|April 1, 1996
Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domainT Izumi, T Hashiguchi, G Castaman, et al.
Dental Cadmos|January 31, 1987
[Tooth extractions in patients with hemophilia and von Willebrand's disease]R Vangelisti, D N Rositani, A Pagnacco, et al.
Blood|April 1, 1984
Liver dysfunction rather than intravascular coagulation as the main cause of low protein C and antithrombin III in acute leukemiaF Rodeghiero, P M Mannucci, S Viganò, et al.
British Journal of Haematology|December 1, 1996
A (15;17) translocation not associated with acute promyelocytic leukaemiaE Di Bona, A Montaldi, N Guercini, et al.
Pageof 27