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British Journal of Haematology|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.American Journal of Hematology|June 8, 2001
A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseasesD Gemmati, M L Serino, A Ongaro, et al.Journal of Thrombosis and Haemostasis : JTH|June 18, 2015
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor XA Branchini, M Baroni, F Burini, et al.British Journal of Haematology|March 1, 1990
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogeneF Bernardi, G Marchetti, A Casonato, et al.Human Genetics|July 1, 1992
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)G Marchetti, P Patracchini, D Gemmati, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Thrombotic risk in thalassemic patientsS Moratelli, V De Sanctis, D Gemmati, et al.Free Radical Biology & Medicine|May 9, 2006
The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesisPaolo Zamboni, Marcello Izzo, Silvia Tognazzo, et al.Cytogenetic and Genome Research|August 15, 2013
Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literatureA Castiglione, V Guaran, L Astolfi, et al.Human Genetics|November 1, 1993
Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic regionF Bernardi, P Patracchini, D Gemmati, et al.British Journal of Haematology|June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.Pageof 4