Hamostaseologie

Papers
(The median citation count of Hamostaseologie is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
Mitteilungen aus der Vorstandsarbeit60
Current Topics from the Revised German S2k Guideline on Diagnosis and Treatment of Venous Thromboembolism30
Erratum: Aktueller Bericht der BDDH über die aktuellen gesundheitspolitischen Entwicklungen mit politischer Einordnung27
Medizinforschungsgesetz, Apothekenreform-Gesetz, Telemedizin Blutspende-Verordnung, Erweiterung der Dokumentationspflichten im Deutschen Hämophilieregister (DHR)26
GTH 2025 ARTE: The Art in Science – Curiosity and Creativity22
Übergewicht und Adipositas erhöht Risiko für venöse Thromboembolien21
Mansoor’s self-report tool for cardiovascular risk assessment predicts adverse in-hospital events in patients with pulmonary embolism19
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Participation of T helper cell-mediated negative regulation of coagulation in human arterial thrombosis16
Recombinant ADAMTS13 treatment in a pregnant patient with hereditary thrombotic thrombocytopenic purpura14
Current diagnostic and therapeutic standard of iliac vein compression syndrome (May-Thurner syndrome) in children, adolescents and young adults. A survey among national thrombosis experts14
Immune tolerance achievement by low dose factor VIII in PUPs and MTPs under prophylaxis with emicizumab: two case reports13
Diagnostic challenges of Thrombotic Thrombocytopenic Purpura: Results from a cohort of 3,100 individual patients in a time period of 21 months12
Preanalytical quenching of FVIII using FVIII-inhibitors improves the specificity of functional emicizumab testing12
Gene Therapy of Haemophilia: Current Status and Future Directions10
Possible immune reaction to COVID-19 vaccination - a case report10
Thrombopoietin external quality assessment – laboratory results and method precision9
Inter-laboratory comparison of plasma efanesoctocog alfa measurements9
Shifted TFPI/tissue factor balance drives paradoxically delayed thrombin initiation in active pediatric IBD9
Therapeutic options to treat immunothrombosis mediated by platelet activating histone/anti-histone immune complexes9
Knowledge graph-driven curation of heme-TLR4 interactions in inflammatory pathways9
Von Willebrand Factor at the Crossroads of Hemostasis and Inflammation9
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Sulodexid: Neue Hoffnung bei retinalen Gefäßerkrankungen8
Immune Thrombocytopenia: Characteristics of the Population and Treatment Methods—One-Center Experience8
Komplementdysregulation als Biomarker für Post Covid8
Die Gesellschaft für Thrombose- und Hämostaseforschung e.V. informiert8
Development of Antidrug Inhibitory Antibodies against Polyethylene Glycol after Treatment with PEGylated Factor VIII Therapeutic7
Subsegmental Pulmonary Embolism7
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Checkpoint Inhibitors, CAR T Cells, and the Hemostatic System: What Do We Know So Far?7
Impaired hemostatic capacity in patients with low von Willebrand factor6
Platelets are pre-activated during thrombocytopenia in a subset of early malaria infections6
Efficacy of emicizumab prophylaxis in patients with severe hemophilia A in Germany: Follow-up evaluation of real-life-data documented by smart medication eDiary6
A Survey on anticoagulation in patient with ITP6
Splanchnic Vein Thrombosis: The State-of-the-Art on Anticoagulant Treatment6
Insights in pain processing of affected versus non-affected structures6
Exploring red blood cells as a novel tolerogenic approach for Factor VIII inhibitors employing immuno-dominant FVIII derived peptides presented on MHC class II6
Immune modulation by the endothelial protein C receptor (EPCR) in cancer progression6
NXT007 prophylaxis in people with haemophilia A with or without FVIII inhibitors: a global phase I/II multiple-ascending-dose study.5
Histological characterisation of intraluminal thrombi from patients with abdominal aortic aneurysm5
Hemolysis-derived heme meets protein Z: Insights into a novel heme-binding anticoagulant protein5
Blutspende auch ohne Arztanwesenheit und aktueller Stand des Apothekenreform-Gesetzes (ApoRG)5
Influenza infections destabilize established immune tolerance in HemA mice5
Evidence in Haemophilia Assessment: The Haemophilia Joint Health Score5
The Current Evidence of Pulmonary Embolism Response Teams and Their Role in Future5
Investigating the role of GABARAPs protein family in FVIII secretion5
Novel humanized mouse model of heparin-induced thrombocytopenia5
Association between FIX levels & bleeding rates in hemophilia B patients receiving rFIXFc or N9-GP5
Venous Thromboembolism in Women with Cancer with an Additional Focus on Breast and Gynecological Cancers5
Adults with severe or moderately severe haemophilia B receiving etranacogene dezaparvovec in the HOPE-B phase 3 trial experience a stable increase in mean Factor IX activity levels and durable haemost5
Primäre Immunthrombozytopenie: Erhöhtes Krebsrisiko für Erwachsene5
Unexpected Loss of FVIII Recovery Due to Product-Specific Anti-Drug Antibodies in a Mild Hemophilia A Patient Treated with Efanesoctocog Alfa5
Hypofibrinogenemia is linked to hyperinflammation in patients receiving CAR T-cell therapy5
Platelets in Myocardial Ischemia/Reperfusion Injury5
Die Gesellschaft für Thrombose- und Hämostaseforschung e.V. informiert5
Vitamin D deficiency in adult patients with primary immune thrombocytopenia (ITP) from the Vienna ITP Biobank5
Connecting the Dots: Reflections on a vibrant Year in Haemostasis Research5
Platelet sensitivity to GPVI stimulation decreases during platelet recovery after apheresis4
Platelet Dynamics and Clinical Outcomes in Patients with Heparin-Induced Thrombocytopenia – Single Center Experience4
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Reference Intervals in Coagulation Analysis4
Clinical outcome and cost analyses in adult patients with acquired hemophilia A- a single center, retrospective analysis.4
Adenoviral Core Protein VII-Driven Cross-Reactivity of Anti-PF4 Antibodies as a Trigger for VITT Pathogenesis4
Management of Antithrombin Deficiency in Pregnancy4
Altered plasma factors in congenital thrombophilia suppressing platelet glycoprotein VI activation4
Use of concizumab in children with severe hemophilia B and factor IX-inhibitors4
Patient-reported outcomes after upper-extremity deep vein thrombosis due to compression syndromes: A multinational longitudinal retrospective study4
Bleeding Disorder of Unknown Cause: A Diagnosis of Exclusion4
Echtzeit-Bildgebung der durch Blutplättchen induzierten Blutgerinnselbildung und -auflösung zeigt unterschiedliche Auswirkungen von Antikoagulantien3
Runder Tisch zum deutschen Hämophilieregister (DHR), drohender Praxenkollaps, Stand und Zukunft der ambulanten hämostaseologischen Versorgung in Deutschland3
Survey on the care reality of people with mild hemophilia A and B in Germany - the burden of mild hemophilia3
Clinical and Genetic Spectrum of Hereditary Antithrombin Deficiency: Correlation of Type, Functional Activity, and Arterial Thrombotic Risk3
Thrombocytopenia Absent Radius (TAR)-Syndrome: From Current Genetics to Patient Self-Empowerment3
Petition „Vergütung für medizinische Leistungen – Verbesserung der Rahmenbedingungen für die ambulante Versorgung“, ATMP-QS-Richtlinie Hämophilie und aktueller Stand zur Digitalisierung im Gesundheits3
EMIIL - Non-interventional study to investigate the effectiveness of Emicizumab under real-world conditions in pediatric, adolescent, adult and elderly patients with hemophilia A (PwHA) with and witho3
A novel single chain antibody inhibiting lateral fibrin interactions thereby remodeling fibrin clot architecture and accelerating thrombolysis3
Erratum: A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia3
Evaluating the individual risk of venous thrombo-embolism in patients with liver cirrhosis: Usefulness of in vivo and ex vivo thrombin generation parameters3
Durability of bleeding protection and Factor IX activity in individuals with and without adeno-associated virus serotype 5 neutralising antibodies (Titres <1:700) in the phase 3 HOPE-B trial of etr3
Measurement of procoagulant platelets in platelet-rich plasma by flow cytometer for the diagnosis of heparin-induced thrombocytopenia3
Changes in Hemophilia Treatment in the Eastern Part of Germany between 2015 and 2021—Data from the Kompetenznetz Hämorrhagische Diathese Ost (KHDO)2
GTH News2
Gleiches Risiko für schwere kardiovaskuläre Ereignisse nach hämorrhagischem und ischämischem Schlaganfall2
Elevated plasminogen activator inhibitor-1 is not associated with impaired plasmin formation and thrombotic risk after low-grade coagulation activation in vivo2
Mild Factor XI Deficiency in Women with Hypermenorrhea or Prolonged Postoperative Bleeding: A Genotype–Phenotype Analysis2
Decoding the Fibrinogen γβ Nodule (D-Region): First Cryo-EM Insights Toward the Full Hexameric Structure2
Correlation between Platelet-to-Lymphocyte Ratio, Neutrophil-to-Lymphocyte Ratio and Burden of Thrombus with Disease Severity in Patients with Pulmonary Thromboembolism2
Diagnostic Challenges in Acquired Hemophilia A with Concomitant Oral Anticoagulant Use: A Case Series Analysis2
Temporal phosphoproteomics reveals key regulators of procoagulant COAT platelet generation2
Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors2
Tissue Factor Pathway Inhibitor is associated with risk of venous thromboembolism and all-cause mortality in patients with cancer2
Non-clinical pharmacodynamic effects and immunogenicity assessment of prophylactic immune modulation prior to gene therapy dose administration in C57BL/6 mice2
Inhibition of cold-induced apoptosis of platelet concentrates improves platelet functionality and half-life2
Recurrent Venous Thrombosis in a Hypofibrinogenemic Patient Despite a Heterozygous Deletion of the Fibrinogen Gene Cluster and Hemizygous FGB p.Pro265Leu Variant Mimicking a Homozygous Genotype2
Plasma proteomics and collagen biomarkers in people with haemophilia A receiving emicizumab in STASEY2
Antidepressant Agent Use and Risk of Bleeding in Patients with Cancer: Results from the Vienna CAT-BLED study2
Risk Factors for the Progression of Haemophilic Arthropathy – The PUSH-Study2
A new rapid automated clotting assay enables measurement of residual TFPI activity in human plasma2
Immune Response Mechanisms in Haemophilia A2
Inhibition of MicroRNA-122-5p Relieves Myocardial Ischemia-Reperfusion Injury via SOCS12
Digital joint discovery tool to support hemophilia patient education2
Pharmazeutische Unternehmen außerhalb der USA unter Druck2
Telomere length is associated with increased risk of cardiovascular events in hemodialysis patients2
HEM-POWR study: Subgroup analysis evaluating the real-world effectiveness and safety of damoctocog alfa pegol in previously treated patients with haemophilia A in Germany2
Comprehensive DIA-MS profiling of clot and plasma proteomes across immune- and coagulation-deficient mouse models2
Veranstaltung des BDDH im Rahmen der 67. Jahrestagung der Gesellschaft für Thrombose- und Hämostaseforschung in Frankfurt2
On Factor VIII Assay Discrepancies in Post-infusion Samples Obtained from Patients Treated with Efanesoctocog Alfa2
Impact of recalcification on procoagulant COAT platelet generation in PRP samples with low platelet counts2
Prediction of brain cancer-associated thrombosis by imaging-based machine learning: Results from the Vienna Cancer and Thrombosis Study2
The Timed Up and Go Test in Patients with Haemophilia: Assessing Reliability, Validity, and Predictive Variables1
Sequential combinations of rapid immunoassays for quick recognition of heparin-induced thrombocytopenia1
In vitro haemostatic functionality of INTERCEPT (Amotosalen, UVA) pathogen-reduced platelet concentrates is not affected by cold-storage1
Periinterventional management of edoxaban in major procedures: results from the DRESDEN NOAC REGISTRY1
Transfusion älterer Erythrozyten erhöht Mortalität und Thromboembolie-Risiko1
Performance Evaluation of Different FIX Activity Assays for Determining Nonacog Beta Pegol (N9-GP, Refixia) Activity Using Reagent-/Platform-Specific Conversion Factors1
Impact and dynamics of monocyte and platelet activation on clinical outcomes in patients under immune checkpoint inhibitors.1
Interim 52-Week analysis of immunogenicity to the vector capsid and transgene-expressed human FVIII in GENEr8-1, a phase 3 clinical study of valoctocogene roxaparvovec, an AAV5-mediated gene therapy f1
The Use of Large Animal Models in Trauma and Bleeding Studies1
Real-World Effectiveness and Usage of Recombinant Factor IX Fc: Final Data from the B-MORE Study1
Endogenous FVIII activity and procedure-related FVIII use and bleeding: post hoc analysis of GENEr8-11
Treatment of Inherited Platelet Disorders: Current Status and Future Options1
Identification of key regulators of procoagulant COAT platelet generation by quantitative phosphoproteomic analysis and phosphoflow1
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations1
The impact of Syk-inhibition on 5B9 monoclonal HIT antibody-mediated procoagulant platelet formation1
Antiboby mediated Acquired Glanzmann Thrombasthenia – a diagnostic and therapeutic challenge – with Concizumab as Promising Therapeutic Approach: A Case Report1
Correlation between coagulation factor residual activities and detection rate of diseasecausing variants in Rare Bleeding Disorders1
Geringe α-Thrombin/GPIbα-Interaktion trägt möglicherweise zur Hyperreaktivität der Thrombozyten bei COVID-19-Patienten bei1
Analysis of Soluble and Humoral Immunological Parameters During Re-exposure with rFVIIIFc after History of Inhibitors1
Haemostaseological pearls1
Treatment of a patient with von Willebrand disease type 2B and severe thrombocytopenia due to mutation p.V1316M with thrombopoietin receptor agonist Avatrombopag1
Bleeding Risk in Patients with Cancer1
Ontogeny of peripheral blood platelet GPIIb/IIIa activation and granule release in preterm and term neonates1
A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Crovalimab as Add-On Therapy in Patients with Antiphospholipid Syndrome and Recurrent Thrombosis1
Improved blood analysis panel for the early detection of thromboses and thrombotic risk factors1
Direct oral anticoagulation in transplant recipients – long-term Follow-up from the Prospective Dresden NOAC Registry (NCT01588119)1
Clinical Course and Outcomes of Thrombotic Thrombocytopenic Purpura in Young Adults with Systemic Lupus Erythematosus: A Case Series from a Tertiary Hospital1
Efficacy, safety, and quality of life 5 years after valoctocogene roxaparvovec gene transfer1
Recurrent Venous Thromboembolism in Patients on Anticoagulation: An Update Based on the Revised AWMF S2k Guideline1
Subsequent vaccinations in VITT patients other than SARS-CoV2 vaccination1
From Case Reports to Cohort Studies: The Many Faces of Clinical Research in Thrombosis and Haemostasis1
NET formation contributes to clinical relapses but not ADAMTS13 biomarker relapses in immune-mediated thrombotic thrombocytopenic purpura1
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A Review of FXIa Inhibition as a Novel Target for Anticoagulation1
Navigating the Diagnostic and Clinical Spectrum of Thrombocytopenia and Thrombocytopathy: Lessons from a Case Series1
The effect of prophylactic corticosteroid treatment on adeno-associated virus-mediated gene therapy and potential mechanisms of action1
Extravascular distribution of factor IX: evidence and relevance for hemophilia B replacement therapy1
Saliva and urine from persons with hemophilia A trigger coagulation bypassing factor VIII1
Prevalence of Synovial Hypertrophy in 428 Patients with Haemophilia A1
In vivo modulation of the protein C pathway by THBD and PROCR gene variants1
Endothelial protein C receptor signaling regulates myeloid-biased hematopoiesis under stress and in aging1
In Japan 40% Blutungskomplikationen während ECMO-Therapie bei COVID-191
Primary Prevention of Cancer-Associated Thrombosis: Current Perspectives1
Monitoring of argatroban in COVID-19 ICU patients: a prospective study comparing aPTT, point-of-care viscoelastic testing with ECA-test and dTT to LC/MS/MS0
The phenotypic and genetic assessment of hereditary antithrombin deficiency in 215 patients from the Rhein-Ruhr area in Germany0
Comparison of Performances among Four Bleeding-Prediction Scores in Elderly Cancer Patients with Venous Thromboembolism0
Welcome0
Immunofluorescence microscopy of the blood smear in myeloproliferative neoplasms0
Dental Surgery without Clotting Factor Replacement Therapy during Continued Prophylaxis with Marstacimab, an Inhibitory TFPI Monoclonal Antibody0
Preexisting Chronic Thromboembolic Pulmonary Hypertension in Acute Pulmonary Embolism? A Case Report and Discussion0
Grundlagen zur Anwendung von Andexanet0
Potenzielle globale Gerinnungsparameter für Therapiemonitoring unter Emicizumab0
Laboratory Monitoring in Patients Receiving Emicizumab0
Direct Oral Anticoagulants: Laboratory Challenges and Antidotes0
Utility of ACMG classification to support interpretation of molecular genetic test results in patients with FVII deficiency0
Impaired thrombin generation as a reproducible feature of bleeding disorder of unknown cause0
IMPROVE: Identifying Molecular Determinants to Personalize Response and Optimize Treatment in von Willebrand Disease and Hemophilia0
Agenesis of vena cava inferior (AVCI) and Hypereosinophilic Syndrome (HES): two rare causes of severe thrombosis and its challenging treatment in adolescents0
Factor VIII assay discrepancies in post-infusion samples obtained from patients treated with efanesoctocog alfa0
Glycoprotein-specific antibodies induce distinct platelet destruction pathways in ITP0
Cancer-Associated Venous Thromboembolism—Diagnostic and Therapeutic Considerations: An Update Based on the Revised AWMF S2k Guideline0
The Use of DOACs in Pediatrics: Current Therapeutic and Prophylactic Indications, Cardiac Indications, and Real-World Evidence—A Review0
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Novel Ultrasound Markers of Synovial Tissue Function to Differentiate the Severity of Synovial Proliferation in Patients with Hemophilia: A Cross-Sectional Analysis0
Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics0
Diagnosis and Therapy of Visceral Vein Thrombosis: An Update Based on the Revised AWMF S2k Guideline0
GTH News0
Defective platelet PAR1 signaling is associated with perioperative bleeding and impaired host defense0
A hierarchical network of Src, Syk, Btk and PKC controls GPVI-dependent human platelet activation0
Update on Cancer-Associated Venous Thromboembolism in Children0
International normalized ratio (INR) and aPTT values associated with dabigatran plasma levels≤20 ng/ml – Development and validation of a predictive model including 164 patients.0
Aggregates of non-muscle myosin IIA in the erythrocytes associate with GATA1-related thrombocytopenia0
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Correction: Oxidative Stress, NADPH Oxidases, and Arteries0
Laboratory Findings, Medical Imaging, and Clinical Outcome in Children with Cerebral Sinus Venous Thrombosis0
Platelet hyperactivation and neutrophil extracellular traps promote thrombo-inflammation and glomerular endothelial dysfunction in diabetic kidney disease0
Cytokine dynamics following joint injury in hemophilia A mice0
Phase 3 study of the efficacy, pharmacokinetics, immunogenicity and safety of von Willebrand Factor/Factor VIII concentrate in patients with severe von Willebrand Disease under 6 years of age0
Nachruf auf Rainer B. Zotz und Ankündigung der BDDH-Veranstaltung auf der GTH in Frankfurt 20230
Implications of the API-CAT Trial for Extended Secondary Prophylaxis of Cancer-associated Venous Thromboembolism: Guidance from an Expert Panel0
Comparative transcriptome profile analysis on early T2DM-aggravated atherosclerotic mouse aortas0
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Die Gesellschaft für Thrombose- und Hämostaseforschung e.V. informiert0
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Pitfalls in Coagulation Testing0
Platelet GPIIbIIIa enriched membrane protrusions (Tether) in healthy and diseased individuals0
Developing an assay to distinguish between HIT and VITT antibodies0
The impact of enhanced platelet turnover on platelet reactivity in healthy humans0
Postpartum acquired hemophilia A in two women with previously undiagnosed von Willebrand disease type 2N -unraveling two rare diagnoses0
Treatment of Bleeding Episodes with Efanesoctocog Alfa in Children: XTEND-ed Second Interim Analysis0
The Post-VTE Functional Status Scale for assessment of functional limitations in patients with venous thromboembolism: construct validity and responsiveness in a prospective cohort study0
Mitochondrial Calcium Uniporter: A Potential Target to Modulate Procoagulant Platelets0
Post–Pulmonary Embolism Syndrome: An Update Based on the Revised AWMF-S2k Guideline0
Overview on Rare Congenital Bleeding Disorders and Epidemiological Data from the German Haemophilia Registry (DHR) and a Survey in Germany, Austria, and Switzerland0
Thrombozyten: Blutstillung ohne Gerinnselbildung0
Erratum to: Congenital Fibrinogen Deficiencies: Not So Rare0
Alternative polyadenylation regulates VEGF-coreceptor NRP10
Women and Hereditary Bleeding Disorders0
Antithrombotic Therapy in Cancer Patients with Cardiovascular Diseases: Daily Practice Recommendations by the Hemostasis Working Party of the German Society of Hematology and Medical Oncology (DGHO) a0
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Association of age with the ISTH-BAT score and prevalence of bleeding symptoms in patients with bleeding disorder of unknown cause: results from the Vienna bleeding biobank0
Relation of FVIII activity levels with global assays of hemostasis in persons with hemophilia A0
Direct Oral Anticoagulants for Pulmonary Embolism0
Procoagulant Platelets and Thrombin Generation in Glanzmann Thrombasthenia: Insights into Bleeding and the Failing Compensatory Mechanism with Desmopressin on Platelets0
Indirect treatment comparisons of the gene therapy etranacogene dezaparvovec (CSL222) vs. extended half-life Factor IX therapies for severe or moderately severe hemophilia B0
A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia0
High Prevalence of F2 20210G > A in Splanchnic Vein Thrombosis and Cerebral Venous Sinus Thrombosis: A Retrospective Cohort Study of Patients with Thrombosis in Atypical Sites0
Evolution of joint health and physical activity in people with haemophilia A without factor VIII inhibitors switching to emicizumab prophylaxis: 12-month interim analysis of the BEYOND ABR study0
Blutverlust bei Frauen im gebärfähigen Alter aufgrund oraler Antikoagulanzien gegen venöse Thromboembolien0
Evaluation of the protein C pathway in critically ill patients with severe COVID-19 as compared to bacterial sepsis0
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A Cross-sectional Analysis of Treatment in PUPs in 2021 in Germany – First Data from the GEPHARD Study Group0
G-BA entscheidet Festgruppe für (plasmatischen) Blutgerinnungsfaktor VIII0
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P2Y12-Inhibitoren hemmen Thrombozyten-induzierte Monozytenaktivierung0
Challenging Situations in the Treatment of Cancer-Associated Thrombosis0
Platelet responsiveness in the post-acute phase of pulmonary embolism0
At the forefront of the introduction of gene therapy in hemophilia A and B: Design and implementation of an innovative software platform ("smart medication Gene") for gene therapy0
Simultaneous detection of factor VIII and emicizumab0
Gut Microbiota as a Modulator of Age-related Arterial Thrombosis0
Assessment of platelet abnormalities in patients with DiGeorge Syndrome by immunofluorescence microscopy on the blood smear0
Haemostaselogy meets Gender-medicine – Pulmonary embolism in girls0
Efficacy and Safety of Marstacimab in Participants With Severe Hemophilia A or B Without Inhibitors: Hemophilia Subgroup Results From the Phase 3 BASIS Trial and its Open-Label Extension0
VTE Risk Assessment and Prevention in Pregnancy0
Congenital Dysfibrinogenemia with Recurrent Venous Thrombosis and Concomitant von Willebrand Syndrome: A Case Report0
Thromboprophylaxis in pregnant Women with a History of Venous Thromboembolism and/or Thrombophilia – Demographic Data and Implementation of Pharmacological Thromboprophylaxis: Preliminary Results from0
Multisite Thrombosis in a Patient with Paroxysmal Nocturnal Hemoglobinuria0
Disorders of Thrombosis and Hemostasis in Cancer0
Platelets and Sera from Donors of Convalescent Plasma after Mild COVID-19 Show No Procoagulant Phenotype0
Structure functional insights on FXIII-B subunit from models and biophysical structures.0
Thrombozytopenie: Sind Thrombozytentransfusionen vor Legen eines ZVK verzichtbar?0
Pulmonary Embolism: Don't Start Me to Talkin'0
Postthrombotisches Syndrom: SOX-PTS-Score und Méan-Modell zeigen beste Prädiktion0
Involvement of GPVI in FVIII-platelet interactions and PS exposure0
The effect of DNA methylation on inhibitor development in haemophilia A patients treated with FVIII concentrates0
Leveraging medical-AI to speed up Cold Agglutinin Disease detection0
Defining indications for thrombophilia testing – a modified Delphi consensus study in Switzerland0
Randomized-controlled cross-over pilot study on the effectiveness of manual lymphatic drainage in patients with hemophilic arthropathy0
Understanding Congenital FXI Deficiency: Genetic Diagnosis and Correlation of Variant Detection Rate to Factor XI Activity0
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