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A phase III study comparing secondary long-term prophylaxis versus on-demand treatment with vWF/FVIII concentrates in severe inherited von Willebrand disease.
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- Blood Transfusion (17232007), 2019, v. 17, n. 5, p. 391, doi. 10.2450/2019.0183-18
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- Article
Platelet cut-off for anticoagulant therapy in thrombocytopenic patients with blood cancer and venous thromboembolism: an expert consensus.
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- Blood Transfusion (17232007), 2019, v. 17, n. 3, p. 171, doi. 10.2450/2018.0143-18
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- Article
Current challenges in the diagnosis and management of patients with inherited von Willebrand's disease in Italy: an Expert Meeting Report on the diagnosis and surgical and secondary long-term prophylaxis.
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- Blood Transfusion (17232007), 2018, v. 16, n. 4, p. 371, doi. 10.2450/2017.0354-16
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- Article
Italian daily platelet transfusion practice for haematological patients undergoing high dose chemotherapy with or without stem cell transplantation: a survey by the GIMEMA Haemostasis and Thrombosis Working Party.
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- Blood Transfusion (17232007), 2016, v. 14, n. 6, p. 521, doi. 10.2450/2016.0321-15
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- Article
Are intravenous immunoglobulins really inappropriate in acquired von Willebrand syndrome?
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- Blood Transfusion (17232007), 2012, v. 10, n. 3, p. 402, doi. 10.2450/2011.0091-11
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- Article
Activated prothrombin complex concentrate (FEIBA<sup>®</sup>) in acquired haemophilia A: a large multicentre Italian study – the FAIR Registry.
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- British Journal of Haematology, 2019, v. 184, n. 5, p. 853, doi. 10.1111/bjh.15175
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- Article
Von Willebrand factor and fibrinolytic parameters during the desmopressin test in patients with Cushing's disease.
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- British Journal of Clinical Pharmacology, 2011, v. 71, n. 1, p. 132, doi. 10.1111/j.1365-2125.2010.03812.x
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- Article
Use of the von Willebrand factor concentrate with low factor VIII content to manage patients with inherited von Willebrand disease requiring surgical or secondary long‐term prophylaxis: An expert opinion paper from an Italian panel.
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- European Journal of Haematology, 2022, v. 109, n. 2, p. 121, doi. 10.1111/ejh.13785
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- Article
A systematic overview of the first pasteurised VWF/FVIII medicinal product, Haemate<sup>®</sup>P/ Humate<sup>®</sup>-P: History and clinical performance.
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- European Journal of Haematology, 2008, v. 80, p. 3, doi. 10.1111/j.1600-0609.2008.01049.x
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- Article
Type II H von willebrand disease: New structural abnormality of plasma and platelet von willebrand factor in a patient with prolonged bleeding time and borderline levels of ristocetin cofactor activity.
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- American Journal of Hematology, 1989, v. 32, n. 4, p. 287, doi. 10.1002/ajh.2830320409
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- Article
Extracorporeal Shockwave Lithotripsy in Patients Treated with Antithrombotic Agents.
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- Journal of Endourology, 2001, v. 15, n. 3, p. 237, doi. 10.1089/089277901750161656
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- Article
Evaluation and management of postpartum hemorrhage: consensus from an international expert panel.
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- Transfusion, 2014, v. 54, n. 7, p. 1756, doi. 10.1111/trf.12550
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- Article
Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients.
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- American Journal of Hematology, 2012, v. 87, n. 9, p. 870, doi. 10.1002/ajh.23265
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- Article
Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesis.
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- American Journal of Hematology, 2011, v. 86, n. 8, p. 650, doi. 10.1002/ajh.22070
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- Article
The impact of bleeding history, von Willebrand factor and PFA-100<sup>®</sup> on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM-1VWD.
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- British Journal of Haematology, 2010, v. 151, n. 3, p. 245, doi. 10.1111/j.1365-2141.2010.08333.x
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- Article
Von Willebrand Disease: Gaining a global perspective.
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- Haemophilia, 2023, v. 29, n. 4, p. 1104, doi. 10.1111/hae.14804
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- Article
Sixth Åland Island Conference on von Willebrand disease.
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- Haemophilia, 2022, v. 28, p. 3, doi. 10.1111/hae.14495
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- Article
Efficacy and safety evaluation of Fanhdi<sup>®</sup>, a plasma‐derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures: A prospective clinical study.
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- Haemophilia, 2022, v. 28, n. 1, p. e23, doi. 10.1111/hae.14453
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- Article
Von Willebrand factor in high-purity factor VIII complex concentrates: chaperone protein or key to therapies? A meeting report.
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- 2008
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- Publication type:
- Report
Current Management of Patients with Severe von Willebrand Disease Type 3: A 2012 Update.
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- Acta Haematologica, 2012, v. 128, n. 2, p. 88, doi. 10.1159/000338208
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- Article
Current Management of Patients with Severe von Willebrand Disease Type 3: A 2012 Update.
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- Acta Haematologica, 2012, v. 128, n. 2, p. 88, doi. 10.1159/000338208
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- Article
Impact of therapeutic drug monitoring of antiretroviral drugs in routine clinical management of patients infected with human immunodeficiency virus and related health care costs: a real-life study in a large cohort of patients.
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- ClinicoEconomics & Outcomes Research, 2014, v. 6, p. 341, doi. 10.2147/CEOR.S58036
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- Article
Studies of multimerin in patients with von Willebrand disease and platelet von Willebrand factor deficiency.
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- British Journal of Haematology, 1998, v. 103, n. 1, p. 20, doi. 10.1046/j.1365-2141.1998.00943.x
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- Article
Proteolysis of von Willebrand factor is decreased in acute promyelocytic leukaemia by treatment with all-trans-retinoic acid.
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- British Journal of Haematology, 1996, v. 92, n. 3, p. 733, doi. 10.1046/j.1365-2141.1996.401939.x
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- Article
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand disease.
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- British Journal of Haematology, 1994, v. 86, n. 2, p. 327, doi. 10.1111/j.1365-2141.1994.tb04734.x
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- Article
Type I von Willebrand disease, subtype 'platelet low': decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cells.
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- British Journal of Haematology, 1993, v. 83, n. 1, p. 88, doi. 10.1111/j.1365-2141.1993.tb04636.x
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- Article