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Results: 1-7 |
Results: 7

Authors: Peyvandi, F Jenkins, PV Mannucci, PM Billio, A Zeinali, S Perkins, SJ Perry, DJ
Citation: F. Peyvandi et al., Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency, THROMB HAEM, 84(2), 2000, pp. 250-257

Authors: Zeinali, S Duca, F Zarbakhsh, B Tagliabue, L Mannucci, PM
Citation: S. Zeinali et al., Thrombophilic mutations in Iran, THROMB HAEM, 83(2), 2000, pp. 351-352

Authors: Peyvandi, F Mannucci, PM Bucciarelli, P Zeinali, S Akhavan, S Sacchi, E Merlini, PA Perry, DJ
Citation: F. Peyvandi et al., A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardialinfarction, BR J HAEM, 108(2), 2000, pp. 247-253

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

Authors: Duga, S Asselta, R Santagostino, E Zeinali, S Simonic, T Malcovati, M Mannucci, PM Tenchini, ML
Citation: S. Duga et al., Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion, BLOOD, 95(4), 2000, pp. 1336-1341

Authors: Safavi, A Abdollahi, H Sedaghatpour, F Zeinali, S
Citation: A. Safavi et al., Kinetic spectrophotometric determination of V(IV) in the presence of V(V) by the H-point standard addition method, ANALYT CHIM, 409(1-2), 2000, pp. 275-282

Authors: Akhavan, S Rocha, E Zeinali, S Mannucci, PM
Citation: S. Akhavan et al., Gly319 -> Arg substitution in the dysfunctional prothrombin Segovia, BR J HAEM, 105(3), 1999, pp. 667-669
Risultati: 1-7 |