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Haematologica|July 1, 1997
The clinical course of deep-vein thrombosis. Prospective long-term follow-up of 528 symptomatic patientsP Prandoni, S Villalta, P Bagatella, et al.
Thrombosis and Haemostasis|October 6, 1998
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasmaE Castoldi, M Kalafatis, B Lunghi, et al.
Blood|November 9, 2000
Risk for subsequent venous thromboembolic complications in carriers of the prothrombin or the factor V gene mutation with a first episode of deep-vein thrombosisP Simioni, P Prandoni, A W Lensing, et al.
Thrombosis Research|March 15, 2001
A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian familyP Simioni, F Vianello, M Kalafatis, et al.
Thrombosis and Haemostasis|August 1, 1996
Deep venous thrombosis and lupus anticoagulant. A case-control studyP Simioni, P Prandoni, E Zanon, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1980
The congenital factor VII abnormalities (dysproconvertinemias). The genetic plot thickensA Girolami
Archivos Del Instituto De Cardiologia De Mexico|July 10, 1998
Low molecular weight heparins in clinical practice: unsolved or partially solved problemsA Girolami
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1987
A tentative classification of AT III congenital abnormalitiesA Girolami
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|November 8, 2001
Idiopathic deep vein thrombosis and subsequent cancer: suggestions for a patient-oriented and practical approachA Girolami
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1978
Evidence against the presence of "inhibitors" in coumarin treated patientsA Girolami
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