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Results: 1-8 |
Results: 8
Reliable estimates of plasma protein S levels: Are we getting any closer?
Authors: Faioni, EM
Citation: Em. Faioni, Reliable estimates of plasma protein S levels: Are we getting any closer?, THROMB HAEM, 86(5), 2001, pp. 1139-1140
A 23bp insertion in the endothelial protein C receptor (EPCR) gene impairsEPCR function
Authors: Biguzzi, E Merati, G Liaw, PCY Bucciarelli, P Oganesyan, N Qu, DF Gu, JM Fetiveau, R Esmon, CT Mannucci, PM Faioni, EM
Citation: E. Biguzzi et al., A 23bp insertion in the endothelial protein C receptor (EPCR) gene impairsEPCR function, THROMB HAEM, 86(4), 2001, pp. 945-948
Reduced free protein S levels in patients with inflammatory bowel disease - Prevalence, clinical relevance, and role of anti-protein S antibodies
Authors: Saibeni, S Vecchi, M Valsecchi, C Faioni, EM Razzari, C De Franchis, R
Citation: S. Saibeni et al., Reduced free protein S levels in patients with inflammatory bowel disease - Prevalence, clinical relevance, and role of anti-protein S antibodies, DIG DIS SCI, 46(3), 2001, pp. 637-643
Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss
Authors: Franchi, F Biguzzi, E Cetin, I Facchetti, F Radaelli, T Bozzo, M Pardi, G Faioni, EM
Citation: F. Franchi et al., Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss, BR J HAEM, 114(3), 2001, pp. 641-646
Factor VHR2: An ancient haplotype out of Africa - reasons for being interested
Authors: Faioni, EM
Citation: Em. Faioni, Factor VHR2: An ancient haplotype out of Africa - reasons for being interested, THROMB HAEM, 83(3), 2000, pp. 358-359
Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity
Authors: Faioni, EM Hermida, J Rovida, E Razzari, C Asti, D Zeinali, S Mannucci, PM
Citation: Em. Faioni et al., Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity, BR J HAEM, 108(2), 2000, pp. 265-271
Poor relationship between phenotypes of protein S deficiency and mutationsin the protein S alpha gene
Authors: Hermida, J Faioni, EM Mannucci, PM
Citation: J. Hermida et al., Poor relationship between phenotypes of protein S deficiency and mutationsin the protein S alpha gene, THROMB HAEM, 82(6), 1999, pp. 1634-1638
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (Factor V leiden)
Authors: Faioni, EM Franchi, F Bucciarelli, P Margaglione, M De Stefano, V Castaman, G Finazzi, G Mannucci, PM
Citation: Em. Faioni et al., Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (Factor V leiden), BLOOD, 94(9), 1999, pp. 3062-3066
Risultati: 1-8 |