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The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study

Journal of thrombosis and haemostasis, 2005-12, Vol.3 (12), p.2619-2626

2005

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Ultrasound detects joint damage and bleeding in haemophilic arthropathy: a proposal of a score

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-01, Vol.17 (1), p.112-117

2011

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European retrospective study of real‐life haemophilia treatment

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-01, Vol.23 (1), p.105-114

2017

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Prevalence of Hemostatic Disorders in Adolescents with Abnormal Uterine Bleeding

Journal of pediatric & adolescent gynecology, 2013-10, Vol.26 (5), p.285-289

2013

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HEALTH-RELATED QUALITY OF LIFE IN PATIENTS WITH HEMOPHILIA A OR B WITH INHIBITORS ON CONCIZUMAB PROPHYLAXIS: RESULTS FROM THE PHASE 3 EXPLORER7 STUDY

Hematology, Transfusion and Cell Therapy, 2023-10, Vol.45, p.S458

2023

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Viscosupplementation in haemophilic arthropathy: a long-term follow-up study

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e210-e214

2012

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Hypovitaminosis D and osteopenia/osteoporosis in a haemophilia population: a study in HCV/HIV or HCV infected patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-01, Vol.19 (1), p.126-133

2013

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FRI0488 Ultrasound detects joint damage and bleeding in haemophilic arthropathy: the utility of a score

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A540-A540

2013

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AB0959 The Role of Ultrasonography in the Early Diagnosis of Arthropathy in A not Target Joint of Haemophiliacs

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.1117-1117

2014

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Monitoring the bioavailability of FEIBA with a thrombin generation assay

Journal of thrombosis and haemostasis, 2003-11, Vol.1 (11), p.2374-2380

2003

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AB0611 Hypovitaminosis d and osteopenia/osteoporosis in a haemophilia population

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A976-A976

2013

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Are the standard definitions of osteopenia and osteoporosis appropriate for coinfected patients with haemophilia?

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-09, Vol.19 (5), p.e316-e318

2013

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FRI0489 Haemophilic artropathy: from sonographic scoring to histopathological modifications

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A540-A540

2013

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Patient preference and ease of use for different coagulation factor VIII reconstitution device scenarios: a cross-sectional survey in five European countries [Corrigendum]

Patient preference and adherence, 2015-01, Vol.9 (default), p.243-243

2015

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Agonistic anti-human Fas monoclonal antibody induces fibroblast-like synoviocyte apoptosis in haemophilic arthropathy: potential therapeutic implications

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.e32-e39

2014

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Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2164-2169

2006

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Concomitant Use of rFVIIa and Emicizumab in People with Hemophilia A with Inhibitors: Current Perspectives and Emerging Clinical Evidence

Therapeutics and clinical risk management, 2020-01, Vol.16, p.461-469

2020

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A modular total knee arthroplasty in haemophilic arthropathy

The knee, 2007-08, Vol.14 (4), p.264-268

2007

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Multivariate analysis of factors influencing quality of life and utility in patients with haemophilia

Haematologica (Roma), 2001-07, Vol.86 (7), p.722

2001

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Obstacles to Early Diagnosis and Treatment of Inherited von Willebrand Disease: Current Perspectives

Journal of blood medicine, 2021-01, Vol.12, p.165-175

2021

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Clinical, instrumental, serological and histological findings suggest that hemophilia B may be less severe than hemophilia A

Haematologica (Roma), 2016-02, Vol.101 (2), p.219

2016

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Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Journal of thrombosis and haemostasis, 2012-04, Vol.10 (4), p.622-631

2012

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Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry

Blood, 2012-07, Vol.120 (1), p.39-46

2012

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Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A

Therapeutics and clinical risk management, 2016-06, Vol.2016 (Issue 1), p.1029-1037

2016

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Factor VIII Inhibitor-Bypassing Agents Act by Inducing Thrombin Generation and Can Be Monitored by a Thrombin Generation Assay

Pathophysiology of haemostasis and thrombosis, 2003-01, Vol.33 (1), p.16-22

2003

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The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study

Ultrasound detects joint damage and bleeding in haemophilic arthropathy: a proposal of a score

European retrospective study of real‐life haemophilia treatment

Prevalence of Hemostatic Disorders in Adolescents with Abnormal Uterine Bleeding

HEALTH-RELATED QUALITY OF LIFE IN PATIENTS WITH HEMOPHILIA A OR B WITH INHIBITORS ON CONCIZUMAB PROPHYLAXIS: RESULTS FROM THE PHASE 3 EXPLORER7 STUDY

Viscosupplementation in haemophilic arthropathy: a long-term follow-up study

Hypovitaminosis D and osteopenia/osteoporosis in a haemophilia population: a study in HCV/HIV or HCV infected patients

FRI0488 Ultrasound detects joint damage and bleeding in haemophilic arthropathy: the utility of a score

AB0959 The Role of Ultrasonography in the Early Diagnosis of Arthropathy in A not Target Joint of Haemophiliacs

Monitoring the bioavailability of FEIBA with a thrombin generation assay

AB0611 Hypovitaminosis d and osteopenia/osteoporosis in a haemophilia population

Are the standard definitions of osteopenia and osteoporosis appropriate for coinfected patients with haemophilia?

FRI0489 Haemophilic artropathy: from sonographic scoring to histopathological modifications

Patient preference and ease of use for different coagulation factor VIII reconstitution device scenarios: a cross-sectional survey in five European countries [Corrigendum]

Agonistic anti-human Fas monoclonal antibody induces fibroblast-like synoviocyte apoptosis in haemophilic arthropathy: potential therapeutic implications

Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study

Concomitant Use of rFVIIa and Emicizumab in People with Hemophilia A with Inhibitors: Current Perspectives and Emerging Clinical Evidence

A modular total knee arthroplasty in haemophilic arthropathy

Multivariate analysis of factors influencing quality of life and utility in patients with haemophilia

Obstacles to Early Diagnosis and Treatment of Inherited von Willebrand Disease: Current Perspectives

Clinical, instrumental, serological and histological findings suggest that hemophilia B may be less severe than hemophilia A

Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry

Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A

Factor VIII Inhibitor-Bypassing Agents Act by Inducing Thrombin Generation and Can Be Monitored by a Thrombin Generation Assay

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