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Thrombosis Research|February 1, 1992
A new variant of von Willebrand disease (type II I) with a normal degree of proteolytic cleavage of von Willebrand factorG Castaman, F Rodeghiero, A Lattuada, et al.
American Journal of Hematology|May 1, 1995
Characterization of two cases of acquired transitory von Willebrand syndrome with ciprofloxacin: evidence for heightened proteolysis of von Willebrand factorG Castaman, A Lattuada, P M Mannucci, et al.
Blood|June 15, 1992
Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trialP M Mannucci, P M Tenconi, G Castaman, et al.
Thrombosis and Haemostasis|September 24, 1999
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigationG Castaman, J C Eikenboom, R M Bertina, et al.
Haematologica|May 1, 1992
Fulminant sepsis in adults splenectomized for idiopathic thrombocytopenic purpuraF Rodeghiero, M Frezzato, C Schiavotto, et al.
Journal of Thrombosis and Haemostasis : JTH|March 26, 2011
Prospective evaluation of the clinical utility of quantitative bleeding severity assessment in patients referred for hemostatic evaluationA Tosetto, G Castaman, I Plug, et al.
British Journal of Haematology|December 31, 1997
Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor VG Castaman, B Lunghi, E Missiaglia, et al.
Blood|June 1, 1990
Early deaths and anti-hemorrhagic treatments in acute promyelocytic leukemia. A GIMEMA retrospective study in 268 consecutive patientsF Rodeghiero, G Avvisati, G Castaman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Acquired haemophilia: experience of two Italian centres with 17 new casesE Di Bona, M Schiavoni, G Castaman, et al.
Journal of Thrombosis and Haemostasis : JTH|September 22, 2010
Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficienciesG Castaman, M Platè, S H Giacomelli, et al.
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