Disease: Von Willebrand disease
- A career in solving clinical-pathological conundrums: Heyde syndrome, anti-platelet factor 4 disorders, and microvascular limb ischemic necrosis
- A Compound Heterozygosis of Two Novel Mutations in vWF Exacerbates vWD in a Chinese Pedigree
- A Cross-Sectional Study of Protein Changes Associated with Dementia in Non-Obese Weight Matched Women with and without Polycystic Ovary Syndrome
- A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand disease
- A novel inducible von Willebrand Factor Cre recombinase mouse strain to study microvascular endothelial cell-specific biological processes in vivo
- A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review
- Acquired bleeding disorders
- Acquired von Willebrand syndrome associated with a smoldering multiple myeloma, successfully treated by daratumumab, lenalidomide and dexamethasone
- Acquired von Willebrand syndrome in a patient with monoclonal gammopathy of unknown significance: A case report
- Activated protein C and free protein S in patients with mild to moderate bleeding disorders
- Altered fibrin clot properties are associated with the progression of chronic kidney disease in atrial fibrillation
- An Algorithm for Control of Excessive Perioperative Bleeding and Ecchymosis in Rhinoplasty Patients Based on 4 Decades of Experience
- An unusual cause of bleeding in primary hypothyroidism
- Anemia, Increased Shear Stress, and the Progression of Aortic Stenosis
- Anticoagulation and Antiplatelet Use Among Patients with von Willebrand Disease and Cardiac Disease
- Apixaban-Induced Spontaneous Hemorrhagic Cardiac Tamponade
- Associations of plasma proteomics and age-related outcomes with brain age in a diverse cohort
- Awareness of von Willebrand disease among gynecologists: Investigating the referral of women with heavy menstrual bleeding to hematologists
- Bleeding Disorder of Unknown Cause: A Diagnosis of Exclusion
- Blood group AB is associated with reduced blood loss but also elevated cardiovascular mortality in aortocoronary bypass surgery
- Case report: Peri-procedural hydroxyurea helps minimize bleeding in patients with Essential Thrombocythemia associated with acquired von Willebrand syndrome
- Clusterin knockdown has effects on intracellular and secreted von Willebrand factor in human umbilical vein endothelial cells
- Coagulation Profile in Neonates with Congenital Heart Disease: A Pilot Study
- Complex changes in serum protein levels in COVID-19 convalescents
- Comprehensive investigation of platelet function in patients with cirrhosis
- Congenital Haemostasis Disorders and Urology Surgery: Is It Safe?
- Copines, a Family of Calcium Sensor Proteins and Their Role in Brain Function
- Cost-effectiveness of prophylaxis with recombinant versus plasma-derived VWF in severe von Willebrand disease in the US
- COVID-19 increases extracorporeal coagulation during hemodialysis associated with upregulation of vWF/FBLN5 signaling in patients with severe/critical symptoms
- COVID-19: Not a thrombotic disease but a thromboinflammatory disease
- Diagnosis and treatment challenges in lower resource countries: State-of-the-art
- Diagnosis and treatment of von Willebrand disease in 2024 and beyond
- Early-onset indicators of a hypercoagulable state and clinical complications in a cohort of children with sickle cell trait
- Efficacy of emicizumab therapy in two adult patients with type 3 von Willebrand disease
- EGR1 transcriptionally regulates SVEP1 to promote proliferation and migration in human coronary artery smooth muscle cells
- Evaluating the potential mediating role of ADAMTS13 activity in the relationship between obesity and the severity of COVID-19: A retrospective cohort study
- Factor VIII as a Novel Biomarker for Diagnosis, Prognosis, and Therapy Prediction in Human Cancer and Other Disorders
- Frequency, clinical, and laboratory findings of platelet secretion disorders in patients referred to the specialized coagulation laboratory of the Iranian Blood Transfusion Organization
- Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology
- HELLP Syndrome and Differential Diagnosis with Other Thrombotic Microangiopathies in Pregnancy
- Hereditary hemorrhagic telangiectasia may be the most morbid inherited bleeding disorder of women
- Hereditary TTP/Upshaw-Schulman syndrome: the ductus arteriosus controls newborn survival
- Heyde's syndrome: a challenging case of severe aortic stenosis and gastrointestinal bleeding
- High Glucose Promotes and Aggravates the Senescence and Dysfunction of Vascular Endothelial Cells in Women with Hyperglycemia in Pregnancy
- How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause
- Hydroxychloroquine inhibits hemolysis-induced arterial thrombosis ex vivo and improves lung perfusion in hemin-treated mice
- Immunological Profile and Markers of Endothelial Dysfunction in Elderly Patients with Cognitive Impairments
- Impact of allele-selective silencing of von Willebrand factor in mice based on a single nucleotide allelic difference in von Willebrand factor
- Impact of breastfeeding duration on coagulation in women with and without history of gestational diabetes mellitus
- Increased Complement Activation and Decreased ADAMTS13 Activity Are Associated with Genetic Susceptibility in Patients with Preeclampsia/HELLP Syndrome Compared to Healthy Pregnancies: An Observational Case-Controlled Study
- Inflammasome-Independent Mechanism of NLRP3 Is Critical for Platelet GPIb-IX Function and Thrombosis
- Inhibiting MMP13 Attenuates Deep Vein Thrombosis in a Mouse Model by Reducing the Expression of Pdpn
- Integrin α9β1 deficiency does not impact the development of atherosclerosis in mice
- ISTH bleeding assessment tool and platelet function analyzer in children with mild inherited platelet function disorders
- Knee replacement surgery in a patient with acquired von Willebrand disease: a case study with recommendations for patient management
- Mechanism of astragaloside Ⅳ combined with Panax notoginseng saponins in regulating angiogenesis to treat cerebral ischemia based on network pharmacology and experimental verification
- Mechanisms of endothelial activation, hypercoagulation and thrombosis in COVID-19: a link with diabetes mellitus
- Mental health in persons with von Willebrand disease in the United States - a large national database study
- Misdiagnosis of type 2B von Willebrand disease as immune thrombocytopenia in a thrombocytopenic patient
- Modern diagnostic methods for early assessment of the abdominal involvement in Schonlein-Henoch disease
- Molecular Interactions Required for Activation of Complement Component C2 Include Exosites Located on the Serine Protease Domain of C1s and Mannose-Binding Lectin Associated Protease-2
- Mortality, cardiac and cerebral damages reduction by IL-1 inhibition in a murine model of TTP
- MSCTA imaging analysis of autologous arteriovenous fistula dysfunction in maintenance hemodialysis patients
- Navigating the challenges: a case report on managing a complicated postpartum course in type 3 von Willebrand disease with alloantibodies
- Network pharmacology analysis and experimental verification of the antithrombotic active compounds of trichosanthis pericarpium (Gualoupi) in treating coronary heart disease
- Novel serum protein biomarker panel for early diagnosis of pancreatic cancer
- O-glycan determinants regulate VWF trafficking to Weibel-Palade bodies
- Orthognathic Surgery in Patients With Von Willebrand's Disease: A Report of Four Cases and Literature Review
- Outcomes Following Total Hip Arthroplasty in Patients Who Have Von Willebrand Disease Depend on Postoperative Anticoagulation
- Platelet activity, coagulation, and fibrinolysis in long-term users of anabolic-androgenic steroids compared to strength-trained athletes
- Platelet Proteome Reveals Novel Targets for Hypercoagulation in Pseudoexfoliation Syndrome
- Predictive value of von Willebrand factor for venous thromboembolism in critically ill patients based on propensity score matching
- Presumptive spontaneous hemothorax associated to thymic involution in a dog with steroid responsive meningitis-arteritis (SRMA)
- Procedural outcomes in children with mild type 1 von Willebrand disease
- Progress in von Willebrand Disease Treatment: Evolution towards Newer Therapies
- Proteomic studies in VWA1-related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkers
- Proteomics of serum-derived extracellular vesicles are associated with the severity and different clinical profiles of patients with COVID-19: An exploratory secondary analysis
- Repair of type II paraesophageal hernia with Nissen fundoplication in a patient with von Willebrand disease and spondylolisthesis - a clinical case report
- Self-Assembled DNA Composite-Engineered Mesenchymal Stem Cells for Improved Skin-Wound Repair
- Simple blood tests to diagnose compensated advanced chronic liver disease and stratify risk of clinically significant portal hypertension
- Simple blood tests to diagnose compensated advanced chronic liver disease and stratify the risk of clinically significant portal hypertension
- Small intestinal angiodysplasia and hemorrhage associated with acquired von Willebrand syndrome type 2A secondary to multiple myeloma: Reversal after treatment with IRD regimen (a case report and a brief review of the literature)
- Standardisation of Definition and Management for Bleeding Disorder of Unknown Cause: Communication from the SSC of the ISTH
- Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTH
- Sustained good response to rituximab in acquired von Willebrand syndrome
- Targeting a higher plasma VWF level at time of delivery in pregnant individuals with von Willebrand disease: Outcomes at a single-institution cohort study
- The association between endothelial function and autoimmune thyroiditis induced by iodine excess
- The Interplay between Liver Sinusoidal Endothelial Cells, Platelets, and Neutrophil Extracellular Traps in the Development and Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease
- The role of the specialist nurse in comprehensive care for bleeding disorders in Europe: An integrative review
- Transcriptional and functional profiling identifies inflammation and endothelial to mesenchymal transition as potential drivers for phenotypic heterogeneity within a cohort of Endothelial Colony Forming Cells
- Transcriptional and functional profiling identifies inflammation and endothelial-to-mesenchymal transition as potential drivers for phenotypic heterogeneity within a cohort of endothelial colony forming cells
- Type 2M/2A von Willebrand disease: a shared phenotype between type 2M and 2A
- Ultrasound in addition to clinical assessment of acute musculoskeletal complaints in bleeding disorders: impact on patient management
- Unfolded Von Willebrand Factor Binds Protein S and Reduces Anticoagulant Activity
- Use of crushed tranexamic acid tablets in water for paediatric patients with bleeding disorders
- Validation of Baveno VII criteria and other non-invasive diagnostic algorithms for clinically significant portal hypertension in hepatitis delta
- Variant mapping using mass spectrometry-based proteotyping as a diagnostic tool in Von Willebrand Disease
- Von Willebrand Disease and Pregnancy: Management Protocol From Labor to the Postpartum Period
- Von Willebrand factor for outcome prediction within different clinical stages of advanced chronic liver disease
- Von Willebrand factor: a possible biomarker for disease activity in vasculitis