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The role of von Willebrand factor in hemorrhagic and thrombotic disorders.Bleeding from gastrointestinal angioectasias is not related to bleeding disorders - a case control studyPregnancy and delivery in women with von Willebrand's disease and different von Willebrand factor mutations.Treatment of patients with von Willebrand disease.In vivo gene transfer strategies to achieve partial correction of von Willebrand disease.Generation and optimization of the self-administered bleeding assessment tool and its validation as a screening test for von Willebrand disease.Von Willebrand's disease: clinical management.Advances in the diagnosis and management of von Willebrand disease.Diagnostic approach to inherited bleeding disorders.Management of inherited von Willebrand disease in 2007.Prophylaxis of bleeding episodes in patients with von Willebrand's disease.The evolution and value of bleeding assessment tools.The management of patients with congenital von Willebrand disease during surgery or other invasive procedures: focus on antihemophilic factor/von Willebrand factor complex.Gynecological and obstetrical manifestations of inherited bleeding disorders in women.Management of bleeding disorders in adults.An update on type 2B von Willebrand disease.Microparticle analysis in disorders of hemostasis and thrombosis.Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations.Plasma levels of plasminogen activator inhibitor-1 and bleeding phenotype in patients with von Willebrand disease.Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study.Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding.An Integrated Approach to von Willebrand Disease and Surgical Myocardial Revascularization.Orthopaedic surgery in patients with von Willebrand disease.Identification of von Willebrand disease type 1 in a patient with Ehlers-Danlos syndrome classic type.Long-term prophylaxis with intermediate-purity factor VIII concentrate (Haemate P) in a patient with type 3 von Willebrand disease and recurrent gastrointestinal bleeding.Let's Talk Period! Preliminary results of an online bleeding awareness knowledge translation project and bleeding assessment tool promoted on social media.von Willebrand disease: a clinical and laboratory study of sixty-five patients.Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease.Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease.HEMARTHROSIS DUE TO A RARE CAUSE OF HEMORRHAGIC DIATHESIS: Ehlers-Danlos Syndrome
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Clinical diagnosis of von Willebrand disease.
@ast
Clinical diagnosis of von Willebrand disease.
@en
type
label
Clinical diagnosis of von Willebrand disease.
@ast
Clinical diagnosis of von Willebrand disease.
@en
prefLabel
Clinical diagnosis of von Willebrand disease.
@ast
Clinical diagnosis of von Willebrand disease.
@en
P2860
P1433
P1476
Clinical diagnosis of von Willebrand disease.
@en
P2093
Federici AB
P2860
P304
P356
10.1111/J.1365-2516.2004.00991.X
P478
10 Suppl 4
P577
2004-10-01T00:00:00Z