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Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation

British journal of haematology, 2006-07, Vol.134 (2), p.187-195

2006

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P0157 : Adherence and safety of beta-blockers in elderly patients with cirrhosis and portal hypertension: A multi-center cross-sectional study

Journal of hepatology, 2015-04, Vol.62, p.S361-S361

2015

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Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi®) in the treatment of von Willebrand disease: a retrospective clinical study

Haemophilia : the official journal of the World Federation of Hemophilia, 2002-11, Vol.8 (6), p.761-767

2002

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The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

The New England journal of medicine, 1999-09, Vol.341 (11), p.801-806

1999

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Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia

Thrombosis and haemostasis, 2001-09, Vol.86 (3), p.800-803

2001

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Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease

Blood reviews, 1991-09, Vol.5 (3), p.155-161

1991

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Genetic risk factors for superficial vein thrombosis

Thrombosis and haemostasis, 1999-10, Vol.82 (4), p.1215-1217

1999

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Factor VII Clotting Assay: Influence of Different Thromboplastins and Factor VII-Deficient Plasmas

Thrombosis and haemostasis, 1991, Vol.65 (2), p.160-164

1991

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Patterns of development of tachyphylaxis in patients with haemophilia and von Willebrand disease after repeated doses of desmopressin (DDAVP)

British journal of haematology, 1992-09, Vol.82 (1), p.87-93

1992

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Purinoceptors on blood platelets: further pharmacological and clinical evidence to suggest the presence of two ADP receptors

British journal of haematology, 1995-10, Vol.91 (2), p.434-444

1995

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Dermatan Sulphate for the Prevention of Postoperative Venous Thromboembolism in Patients with Cancer

Thrombosis and haemostasis, 1999, Vol.82 (7), p.30-34

1999

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Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation

Blood, 2000-10, Vol.96 (7), p.2496-2500

2000

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Identification of a New Congenital Defect of Platelet Function Characterized by Severe Impairment of Platelet Responses to Adenosine Diphosphate

Blood, 1992-12, Vol.80 (11), p.2787-2796

1992

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Assessment of the influence of citrate concentration on the International Normalized Ratio (INR) determined with twelve reagent-instrument combinations

Thrombosis and haemostasis, 1998-08, Vol.80 (2), p.258-262

1998

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Clinical Evaluation of Viral Safety of Coagulation Factor VIII and IX Concentrates

Vox sanguinis, 1993-05, Vol.64 (4), p.197-203

Mannucci, Pier Mannuccio

1993

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Thrombin generation and activity during thrombolysis and concomitant heparin therapy in patients with acute myocardial infarction

Journal of the American College of Cardiology, 1995-01, Vol.25 (1), p.203-209

1995

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Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity

British journal of haematology, 2000-02, Vol.108 (2), p.265-271

2000

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Prevalence of pancreatic disorders in HIV-infected hemophiliacs: diagnostic methods and their clinical significance

Biomedicine & pharmacotherapy, 1994, Vol.48 (2), p.89-93

1994

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Persistent thrombin generation during heparin therapy in patients with acute coronary syndromes

Arteriosclerosis, thrombosis, and vascular biology, 1997-07, Vol.17 (7), p.1325-1330

1997

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Plasma levels of activated protein C in healthy subjects and patients with previous venous thromboembolism: relationships with plasma homocysteine levels

Arteriosclerosis, thrombosis, and vascular biology, 1998-09, Vol.18 (9), p.1371-1375

1998

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Role of ADP in platelet aggregation at high shear: studies in a patient with congenital defect of platelet responses to ADP

British journal of haematology, 1994-12, Vol.88 (4), p.826-829

1994

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Conjugated estrogens for the management of bleeding associated with renal failure

The New England journal of medicine, 1986-09, Vol.315 (12), p.731-735

1986

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ABSENCE OF HYPERHOMOCYSTEINEMIA IN TEN PATIENTS WITH PRIMARY PULMONARY HYPERTENSION

Thrombosis research, 1997-02, Vol.85 (3), p.279-282

1997

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Thrombin Generation Is Not Increased in the Blood of Hemophilia B Patients After the Infusion of a Purified Factor IX Concentrate

Blood, 1990-12, Vol.76 (12), p.2540-2545

1990

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von Willebrand Disease “Vicenza” With Larger-Than-Normal (Supranormal) von Willebrand Factor Multimers

Blood, 1988-01, Vol.71 (1), p.65-70

1988

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Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation

P0157 : Adherence and safety of beta-blockers in elderly patients with cirrhosis and portal hypertension: A multi-center cross-sectional study

Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi®) in the treatment of von Willebrand disease: a retrospective clinical study

The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia

Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease

Genetic risk factors for superficial vein thrombosis

Factor VII Clotting Assay: Influence of Different Thromboplastins and Factor VII-Deficient Plasmas

Patterns of development of tachyphylaxis in patients with haemophilia and von Willebrand disease after repeated doses of desmopressin (DDAVP)

Purinoceptors on blood platelets: further pharmacological and clinical evidence to suggest the presence of two ADP receptors

Dermatan Sulphate for the Prevention of Postoperative Venous Thromboembolism in Patients with Cancer

Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation

Identification of a New Congenital Defect of Platelet Function Characterized by Severe Impairment of Platelet Responses to Adenosine Diphosphate

Assessment of the influence of citrate concentration on the International Normalized Ratio (INR) determined with twelve reagent-instrument combinations

Clinical Evaluation of Viral Safety of Coagulation Factor VIII and IX Concentrates

Thrombin generation and activity during thrombolysis and concomitant heparin therapy in patients with acute myocardial infarction

Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity

Prevalence of pancreatic disorders in HIV-infected hemophiliacs: diagnostic methods and their clinical significance

Persistent thrombin generation during heparin therapy in patients with acute coronary syndromes

Plasma levels of activated protein C in healthy subjects and patients with previous venous thromboembolism: relationships with plasma homocysteine levels

Role of ADP in platelet aggregation at high shear: studies in a patient with congenital defect of platelet responses to ADP

Conjugated estrogens for the management of bleeding associated with renal failure

ABSENCE OF HYPERHOMOCYSTEINEMIA IN TEN PATIENTS WITH PRIMARY PULMONARY HYPERTENSION

Thrombin Generation Is Not Increased in the Blood of Hemophilia B Patients After the Infusion of a Purified Factor IX Concentrate

von Willebrand Disease “Vicenza” With Larger-Than-Normal (Supranormal) von Willebrand Factor Multimers

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