11 results on '"Lunghi, B."'
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2. New in vitro and in vivo strategies to modulate von Willebrand factor gene mutations with dominant-negative effect: OR333
3. Genetic determinants of activated factor VII-antithrombin complex plasma concentration include tissue factor, factor VII and endothelial protein c receptor gene variants: OR050
4. Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors
5. A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease: OC-TH-028
6. Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiency
7. Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation
8. The factor V Glu1608Lys mutation is recurrent in familial thrombophilia
9. Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?
10. A novel mutation (Leu817Pro) causing type 2A von Willebrand disease
11. Molecular bases of CRM sup + factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain
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