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Journal of Thrombosis and Haemostasis : JTH|June 25, 2005
The factor V Glu1608Lys mutation is recurrent in familial thrombophiliaB Lunghi, D Scanavini, E Castoldi, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|July 9, 1999
Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjectsD Gemmati, M Previati, M L Serino, et al.British Journal of Haematology|March 1, 1994
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVIIF Bernardi, D L Liney, P Patracchini, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 6, 2001
The reduced sensitivity of the ProC Global test in protein S deficient subjects reflects a reduction in the associated thrombotic riskD Gemmati, M L Serino, S Tognazzo, et al.Thrombosis and Haemostasis|January 1, 1996
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasmaB Lunghi, L Iacoviello, D Gemmati, et al.The Pharmacogenomics Journal|May 8, 2013
The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancerM M Hagleitner, M J H Coenen, R Aplenc, et al.Pageof 4