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Arquivos De Neuro-Psiquiatria|December 6, 2001
[Cytomegalovirus encephalitis in an immunocompetent patient: clinical, neuropathological and ultrastructural analysis]R Salamano, E Gervaz, G Mañana, et al.
Haematologica|January 1, 1992
Prophylaxis of venous thrombosis after gynaecological surgery: a controlled pilot study of defibrotideG Palareti, G Guazzaloca, C Legnani, et al.
Journal of Thrombosis and Haemostasis : JTH|June 18, 2010
Sex, age and normal post-anticoagulation D-dimer as risk factors for recurrence after idiopathic venous thromboembolism in the Prolong study extensionB Cosmi, C Legnani, A Tosetto, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defectsC Legnani, G Palareti, F Grauso, et al.
Cardiology|January 1, 1995
Complement components and fibrinogen: correlations and association with previous myocardial infarctionA Muscari, C Bozzoli, G Massarelli, 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.
Human Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.
International Angiology : a Journal of the International Union of Angiology|January 1, 1989
Pharmacodynamic effects on blood coagulation of a new low molecular weight heparin (alfa-LMWH) in healthy volunteers and gynecological surgery patientsG Palareti, C Legnani, B Bianchini, et al.
Neuroepidemiology|March 13, 2008
Incidence and prevalence of amyotrophic lateral sclerosis in Uruguay: a population-based studyM C Vázquez, C Ketzoián, C Legnani, et al.
British Journal of Haematology|June 1, 1996
Activated protein C resistance: a comparison between two clotting assays and their relationship to the presence of the factor V Leiden mutationC Legnani, G Palareti, R Biagi, et al.
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