Disease: Blood coagulation disorders- inherited
- A 360-degree perspective on adeno-associated virus (AAV)-based gene therapy for haemophilia: Insights from the physician, the nurse and the patient
- A new hope in Hemophilia A treatment by Factor VIII expression in platelets precursors
- A qualitative study on the perioperative experiences and demands of haemophilic arthropathy patients undergoing total joint replacement
- AAV mediated repression of Neat1 lncRNA combined with F8 gene augmentation mitigates pathological mediators of joint disease in haemophilia
- AAV vectors for long-term gene therapy of hemophilia B: Are we there yet?
- Aberrant methylation and expression of TNXB promote chondrocyte apoptosis and extracullar matrix degradation in hemophilic arthropathy via AKT signaling
- Accuracy and clinical role of digital templating for total knee arthroplasty performed on haemophilic knees
- Acquired factor XIII deficiency and its unprecedented association with multiple myeloma: case report and literature review
- Acquired hemophilia A after SARS-CoV-2 infection: a causal or casual association?
- Acute deep vein thrombosis with concurrent new diagnosis of AL-amyloid-induced factor X deficiency
- After an initial Hermansky-Pudlak syndrome clinical diagnosis, molecular testing reveals variants for oculocutaneous albinism type 1B: A case report
- Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease
- Altered Mental Status in a 19-year-old Male with Hemophilia B
- Anti-inflammatory effect of a novel piperazino-enaminone delivered by liposomes in a mouse model of hemophilic arthropathy
- Antithrombin Deficiency during Venoarterial Extracorporeal Membrane Oxygenation: Extremely Common, but Does It Matter?
- Application of genetic testing for the diagnosis of von Willebrand disease
- Association between cognitive impairment and functional limitations in everyday life in patients with haemophilia in Hong Kong
- Beqvez - another gene therapy for hemophilia B
- Biogenesis of lysosome-related organelles complex-2 is an evolutionarily ancient proto-coatomer complex
- Bleeds and resource use in hemophilia B: retrospective observational study
- Budd-Chiari syndrome associated with congenital afibrinogenaemia reversed after orthotopic liver transplant
- Case Report: Effective management of adalimumab-induced acquired hemophilia A with the CyDRI protocol
- Characterization of zebrafish coagulation cofactors Fviii and Fv mutants and modeling hemophilia A and factor V deficiency
- Clinical Efficacy of Intra-articular Tranexamic Acid Injection in the Management of Hemophilia with Total Hip Arthroplasty: A 24-month Retrospective Cohort Study
- Clinical immunogenicity outcomes from GENEr8-1, a phase 3 study of valoctocogene roxaparvovec, an AAV5-vectored gene therapy for hemophilia A
- Comparison of the kinematic analysis of indoor and outdoor gait in people with haemophilia and total knee replacement
- Congenital FⅦ Deficiency Associated with a Novel Mutation in <em>F7</em> Gene
- Crohn's disease in hemophilic arthropathy patient: a case report
- Early diagnosis of persons with von Willebrand disease using a machine learning algorithm and real-world data
- Efanesoctocog Alfa Prophylaxis for Children with Severe Hemophilia A
- Effects of resistance training on muscle strength in adults with haemophilia: A systematic review and meta-analysis
- Emicizumab prophylaxis in people with hemophilia A and inhibitors: a systematic review and meta-analysis
- Estimated prophylactic dose required to achieve 3% trough as a function of age and concentrate class in multi-country severe WAPPS-Hemo haemophilia patients
- Examining variability in the diagnosis and management of people with bleeding disorders of unknown cause: communication from the ISTH SSC Subcommittee on von Willebrand Factor
- Exploring the Low Uptake of Gene Therapy in Hemophilia
- Extensive ecchymosis and retroperitoneal hemorrhage due to acquired hemophilia-A following influenza vaccination: A case report
- Factor X deficiency and pregnancy
- FLI1 is associated with regulation of DNA methylation and megakaryocytic differentiation in FPDMM caused by a RUNX1 transactivation domain mutation
- florio<sup>®</sup> HAEMO: A Longitudinal Survey of Patient Preference, Adherence and Wearable Functionality in Central Europe
- Functional clinical motor performance tests to assess potential fall risks in patients with haemophilia: A case-control study
- Genetic screening reveals hotspot variants and prevalence rates of Hermansky-Pudlak syndrome in the Chinese population
- Genotype-phenotype analyses of Iranian patients with hemophilia B (Leyden -) and hemophilia B (Leyden +): A single-center study
- Haemophilia and dental procedures; a complex combination
- Haemophilia B therapy: impact of the reimbursability of a long-acting recombinant factor on pharmaceutical expenditure in Italy
- Hemoglobin concentration and body mass index are determinants of plasma von Willebrand factor and factor VIII levels
- Hemophilia Gene Therapy: Another Blessing or Another Curse?
- Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations c.572-1G>A and c.1037A>C in a Chinese pedigree
- Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency
- Humanistic burden of haemophilia A without inhibitors: A cross-sectional analysis of the HemoLIFE study
- Identifying hemophilia B carriers: Utility of aPTT, factor IX levels and ratios of factor IX to other Vitamin K dependent factors
- Illustrated State-of-the-Art Capsules of the ISTH 2024 Congress
- Incidence and treatment-related risk factors of inhibitor development after intensive FVIII replacement for major orthopaedic surgery in previous treated haemophilia A
- Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients
- ISTH clinical practice guideline for treatment of congenital hemophilia A and B based on the Grading of Recommendations Assessment, Development, and Evaluation methodology: considerations for practice management and implementation
- Joint deficiency of coagulation factors VII and IX: a case report
- Joint health and pain in the changing hemophilia treatment landscape
- Kinetic Modeling for BT200 to Predict the Level of Plasma-Derived Coagulation Factor VIII in Humans
- Laparoscopic liver resection for a patient of hepatocellular carcinoma with von Willebrand disease: a case report
- Limited value of testing for factor XIII and α2-antiplasmin deficiency in patients with a bleeding disorder of unknown cause
- Liver health in hemophilia in the era of gene therapy
- Long-Term Safety Analysis of a Fibrinogen Concentrate (RiaSTAP<sup>®</sup>/Haemocomplettan<sup>®</sup> P)
- Minimal interference of concizumab with standard clinical coagulation laboratory assays - An in vitro study
- Neurosurgical bleeding in platelet storage pool disorder: a case report
- NICE recommends new gene therapy for adults with haemophilia B
- Novel treatment strategies for acquired hemophilia A
- Optimizing the management of inherited blood disorders in a changing market: Findings from the AMCP Market Insights Program
- Oral surgery in people with inherited bleeding disorder: A retrospective study
- Outcome measures in hemophilia: current and future perspectives
- Paradigm shifts in haemophilia A therapy with emicizumab prophylaxis in Asia
- Paving the way to factor X deficiency therapies
- Pedigree Analysis and Molecular Mechanism Study of Hereditary Glanzmann Thrombasthenia Caused by Compound Heterozygous Mutation of the ITGA2B Gene
- Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene
- Practical challenges associated with efanesoctocog alfa (ALTUVIIIO) prophylaxis in a 19-month-old male with severe hemophilia A
- Psychometrics of patient-reported outcomes measurement information system in von Willebrand disease, inherited platelet function disorders, and rare bleeding disorders
- Real-world data on the use of emicizumab in patients with haemophilia A with and without inhibitors in Singapore
- Real-world experience of rIX-FP prophylaxis at dosing intervals of 14 days or more in adult patients with haemophilia B in Italy - Results from IDEAL Part B
- Reconstruction of the historic time course of blood-borne virus contamination of clotting factor concentrates, 1974-1992
- Reduced doses of emicizumab achieve good efficacy: Results from a national-wide multicentre real-world study in China
- Regular prophylaxis with activated prothrombin complex concentrates in pediatric hemophilia
- Retrospective chart review of GI bleeding in people with von Willebrand disease
- RNAing toward a new therapy for hemophilia
- ROTEM could be useful for lupus anticoagulant hypoprothrombinemia syndrome
- Self-conducted sonographic monitoring of the knee in patients with haemophilia-A feasibility study
- Spectrum, clinical characteristics and outcome of von Willebrand disease in Oman
- ST-segment elevation myocardial infarction (STEMI) caused by spontaneous coronary artery dissection (SCAD) in a patient with von Willebrand disease
- Study on the Mutation of FⅨ Gene in 31 Patients with Type B Hemophilia
- Subarachnoid Hemorrhage as a Presentation of Hemophilia: A Case Report
- Successful management of an adolescent male with acquired hemophilia-A with intracranial bleeding using emicizumab
- Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study
- Targeting tissue factor pathway inhibitor with concizumab to improve hemostasis in patients with Glanzmann thrombasthenia: an in vitro study
- The impact of von Willebrand factor on fibrin formation and structure unveiled with type 3 von Willebrand disease plasma
- The relevance of MRI findings in joints of persons with haemophilia: Insights from the last decade
- The spectrum of factor XI deficiency in Southeast China: four recurrent variants can explain most of the deficiencies
- The Utility of Thromboelastography in Monitoring Von Willebrand Disease: A Case Report
- Treatment of haemophilia in Austria
- Treatment of thrombotic cardiovascular diseases in people with haemophilia: A Japanese consensus study
- Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics
- Viscoelastic testing guided coagulation management in factor VII deficiency for spinal anaesthesia and caesarean section
- von Willebrand disease
- Von Willebrand's disease in breast surgery: case report