Hamostaseologie

Papers
(The TQCC 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 2021-12-01 to 2025-12-01.)
ArticleCitations
Veranstaltung des BDDH am 03.03.2022 im Rahmen der 66. Jahrestagung der Gesellschaft für Thrombose- und Hämostaseforschung (GTH) in Leipzig42
Mitteilungen aus der Vorstandsarbeit38
Current Topics from the Revised German S2k Guideline on Diagnosis and Treatment of Venous Thromboembolism24
Erratum: Aktueller Bericht der BDDH über die aktuellen gesundheitspolitischen Entwicklungen mit politischer Einordnung22
Medizinforschungsgesetz, Apothekenreform-Gesetz, Telemedizin Blutspende-Verordnung, Erweiterung der Dokumentationspflichten im Deutschen Hämophilieregister (DHR)21
GTH 2025 ARTE: The Art in Science – Curiosity and Creativity19
Übergewicht und Adipositas erhöht Risiko für venöse Thromboembolien19
Mansoor’s self-report tool for cardiovascular risk assessment predicts adverse in-hospital events in patients with pulmonary embolism18
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Participation of T helper cell-mediated negative regulation of coagulation in human arterial thrombosis18
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 reports14
Recombinant ADAMTS13 treatment in a pregnant patient with hereditary thrombotic thrombocytopenic purpura14
Preanalytical quenching of FVIII using FVIII-inhibitors improves the specificity of functional emicizumab testing13
Diagnostic challenges of Thrombotic Thrombocytopenic Purpura: Results from a cohort of 3,100 individual patients in a time period of 21 months13
Asundexian and milvexian: Pharmacodynamic insights from coagulation assays12
Tolerance Breakdown in Hemophilia A Mice is Orchestrated by Bacterial Infection Modulating Antigen-Specific B and T cell Responses12
Possible immune reaction to COVID-19 vaccination - a case report12
Platelet activating histone/anti-histone immune complexes are associated with a new entity of thrombosis and thrombocytopenia syndrome11
A novel assay to quantify extrinsic tenase complexes in body fluids10
ITAM upregulation in platelets after major surgery10
Komplementdysregulation als Biomarker für Post Covid9
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The Current Evidence of Pulmonary Embolism Response Teams and Their Role in Future8
High Prevalence of Plasminogen Activator Inhibitor-1 4G/5G Polymorphism among Patients with Venous Thromboembolism in Kerala, India8
Splanchnic Vein Thrombosis: The State-of-the-Art on Anticoagulant Treatment8
Sulodexid: Neue Hoffnung bei retinalen Gefäßerkrankungen8
Die Gesellschaft für Thrombose- und Hämostaseforschung e.V. informiert8
Immune Thrombocytopenia: Characteristics of the Population and Treatment Methods—One-Center Experience8
Development of Antidrug Inhibitory Antibodies against Polyethylene Glycol after Treatment with PEGylated Factor VIII Therapeutic7
Insights in pain processing of affected versus non-affected structures7
Subsegmental Pulmonary Embolism7
Exploring red blood cells as a novel tolerogenic approach for Factor VIII inhibitors employing immuno-dominant FVIII derived peptides presented on MHC class II7
Impaired hemostatic capacity in patients with low von Willebrand factor7
Platelets in Myocardial Ischemia/Reperfusion Injury7
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Efficacy of emicizumab prophylaxis in patients with severe hemophilia A in Germany: Follow-up evaluation of real-life-data documented by smart medication eDiary7
Gabapentin and pregabalin can be associated with clinically relevant bleeding due to disturbed platelet function – Two case reports6
A Survey on anticoagulation in patient with ITP6
Platelets are pre-activated during thrombocytopenia in a subset of early malaria infections6
Elevated von Willebrand factor levels during anticoagulation predict early recurrence of venous thromboembolism6
Immune modulation by the endothelial protein C receptor (EPCR) in cancer progression6
Long-term management of deep vein thrombosis based on medical history - A prospective cohort analysis5
Checkpoint Inhibitors, CAR T Cells, and the Hemostatic System: What Do We Know So Far?5
Venous Thromboembolism in Women with Cancer with an Additional Focus on Breast and Gynecological Cancers5
Management of Antithrombin Deficiency in Pregnancy5
Hemophilia care from pediatrics to adulthood – a model of joint interdisciplinary guided transition at a Hemophilia Comprehensive Care Center (HCCC)5
Blutspende auch ohne Arztanwesenheit und aktueller Stand des Apothekenreform-Gesetzes (ApoRG)5
Evidence in Haemophilia Assessment: The Haemophilia Joint Health Score5
Assessing the impact of a pulmonary embolism response team on patients presenting with intermediate risk acute pulmonary embolism. A prospective study (ongoing)5
A Vicious Circle of Clonal Haematopoiesis of Indeterminate Potential and Cardiovascular Disease5
Reference Intervals in Coagulation Analysis5
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 haemost4
Increased transfusion requirement in children compared to adults undergoing cardiac surgery4
Differential platelet activation and thrombo-inflammatory mechanisms in early onset and late onset preeclampsia4
Enhanced platelet turnover after acute myocardial infarction in thrombocytopenic mice and GPVI-deficient mice4
GTH News4
Pregnancy complications in female haemophilia patients and carriers of haemophilia A and B- a nationwide survey4
Vitamin D deficiency in adult patients with primary immune thrombocytopenia (ITP) from the Vienna ITP Biobank4
Autoantibody-induced platelet Fc-gamma-RIIA-mediated procoagulant platelets are important drivers of immunothrombosis in antiphospholipid syndrome4
Runder Tisch zum deutschen Hämophilieregister (DHR), drohender Praxenkollaps, Stand und Zukunft der ambulanten hämostaseologischen Versorgung in Deutschland4
Thrombocytopenia Absent Radius (TAR)-Syndrome: From Current Genetics to Patient Self-Empowerment4
Erratum: A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia4
Influenza infections destabilize established immune tolerance in HemA mice4
Management of Hemophilia C (Factor XI Deficiency) in Two Families: A Case Study at the University Hospital of Halle (Saale)4
Targeting antigen-specific B cells in immune mediated thrombotic thrombocytopenic purpura using modular CAR T cells4
Efficacy of Rivaroxaban in Children with Short Bowel Syndrome4
Bleeding Disorder of Unknown Cause: A Diagnosis of Exclusion4
Results of an international survey (ISTH) on the management of therapeutic-intensity unfractionated heparin4
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 Genotype3
Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors3
Petition „Vergütung für medizinische Leistungen – Verbesserung der Rahmenbedingungen für die ambulante Versorgung“, ATMP-QS-Richtlinie Hämophilie und aktueller Stand zur Digitalisierung im Gesundheits3
Measurement of procoagulant platelets in platelet-rich plasma by flow cytometer for the diagnosis of heparin-induced thrombocytopenia3
Survey on the care reality of people with mild hemophilia A and B in Germany - the burden of mild hemophilia3
Influence of coagulation proteases on cognitive function3
Experiences in Routine Genetic Analysis of Hereditary Hemorrhagic, Thrombotic, and Platelet Disorders3
Inhibition of MicroRNA-122-5p Relieves Myocardial Ischemia-Reperfusion Injury via SOCS13
Neuigkeiten zur Ablösung der geplanten Ablösung der In-Vitro-Diagnostika-Richtlinie durch die In-Vitro-Diagnostika-Verordnung (IVDR) 05/2022 und Plasmaversorgung in Deutschland/EU und Fortführung der 3
Hypofibrinolytic dysregulations can be detected of frozen plasma samples using viscoelastic testing3
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
Familial Protein S deficiency with severe venous thromboembolism (VTE)3
Cardiac and Cerebral Arterial Complications of Lemierre Syndrome: Results from a Systematic Review and Individual Patient Data Meta-analysis3
Recognizing inherited platelet disorders on the peripheral blood smear by immunofluorescence microscopy: results of the first international workshop3
Elevated plasminogen activator inhibitor-1 is not associated with impaired plasmin formation and thrombotic risk after low-grade coagulation activation in vivo3
Veranstaltung des BDDH im Rahmen der 67. Jahrestagung der Gesellschaft für Thrombose- und Hämostaseforschung in Frankfurt3
Correlation between Platelet-to-Lymphocyte Ratio, Neutrophil-to-Lymphocyte Ratio and Burden of Thrombus with Disease Severity in Patients with Pulmonary Thromboembolism3
Venous Thrombosis and SARS-CoV-23
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
Echtzeit-Bildgebung der durch Blutplättchen induzierten Blutgerinnselbildung und -auflösung zeigt unterschiedliche Auswirkungen von Antikoagulantien3
The Impact of non-factor VIII therapy in haemophilia A on procoagulant platelets3
Development and evaluation of a novel machine learning algorithm for outpatient thrombophilia diagnosis, management, and venous thrombosis risk stratification3
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Treatment of Inherited Platelet Disorders: Current Status and Future Options2
Endothelial protein C receptor signaling regulates myeloid-biased hematopoiesis under stress and in aging2
Bleeding Risk in Patients with Cancer2
Telomere length is associated with increased risk of cardiovascular events in hemodialysis patients2
Digital joint discovery tool to support hemophilia patient education2
Pharmazeutische Unternehmen außerhalb der USA unter Druck2
Endogenous FVIII activity and procedure-related FVIII use and bleeding: post hoc analysis of GENEr8-12
Acquired von Willebrand Syndrome in Children2
Changes in Hemophilia Treatment in the Eastern Part of Germany between 2015 and 2021—Data from the Kompetenznetz Hämorrhagische Diathese Ost (KHDO)2
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
Gleiches Risiko für schwere kardiovaskuläre Ereignisse nach hämorrhagischem und ischämischem Schlaganfall2
Tissue Factor Pathway Inhibitor is associated with risk of venous thromboembolism and all-cause mortality in patients with cancer2
Communication in Healthcare: Global challenges in the 21st Century2
GTH News2
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
Venous Thromboembolism Issues in Women1
Ontogeny of peripheral blood platelet GPIIb/IIIa activation and granule release in preterm and term neonates1
Isolation of vWF-specific antibody fragments from phage-displayed scFv libraries1
Comparison of closure time and whole blood impedance aggregometry to light transmission platelet aggregometry for the assessment of platelet response to aspirin and P2Y12 inhibitor therapies: a large-1
Treatment of a patient with von Willebrand disease type 2B and severe thrombocytopenia due to mutation p.V1316M with thrombopoietin receptor agonist Avatrombopag1
Guidance-Based Appropriateness of Hemostasis Testing in the Acute Setting1
Cardio-Oncology: A New Discipline in Medicine and Its Relevance to Hematology1
Animal and Cellular Models in Thrombosis and Hemostasis1
The Timed Up and Go Test in Patients with Haemophilia: Assessing Reliability, Validity, and Predictive Variables1
Saliva and urine from persons with hemophilia A trigger coagulation bypassing factor VIII1
Geringe α-Thrombin/GPIbα-Interaktion trägt möglicherweise zur Hyperreaktivität der Thrombozyten bei COVID-19-Patienten bei1
Performance Evaluation of Different FIX Activity Assays for Determining Nonacog Beta Pegol (N9-GP, Refixia®) Activity Using Reagent-/Platform-Specific Conversion Factors1
Subsequent vaccinations in VITT patients other than SARS-CoV2 vaccination1
Transfusion älterer Erythrozyten erhöht Mortalität und Thromboembolie-Risiko1
Sequential combinations of rapid immunoassays for quick recognition of heparin-induced thrombocytopenia1
The Use of Large Animal Models in Trauma and Bleeding Studies1
Use of Vonicog Alpha and Acquired von Willebrand Syndrome, a New Approach: A Case Report1
Primary Prevention of Cancer-Associated Thrombosis: Current Perspectives1
Platelet Dysregulation in the Pathobiology of COVID-191
Long-term outcome of patients with vaccine-induced immune thrombotic thrombocytopenia and cerebral venous sinus thrombosis1
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
Second- and third-generation FVIII-specific CAR Treg responses to FVIII are functionally affected by the combination of FVIII-specific scFvs and intracellular costimulatory domains1
Understanding the biomolecular corona formation at the nano-bio interface1
In Japan 40% Blutungskomplikationen während ECMO-Therapie bei COVID-191
Association Between Major Bleeding and In-Hospital Major Adverse Cardiovascular Events After Percutaneous Coronary Intervention in Acute Coronary Syndromes1
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations1
Successful Secondary Endovascular Intervention in Pediatric Patients with Venous Thromboembolic Events1
GTH News1
Correlation between coagulation factor residual activities and detection rate of diseasecausing variants in Rare Bleeding Disorders1
A Review of FXIa Inhibition as a Novel Target for Anticoagulation1
Endothelial Mechanisms Modulate the Prothrombotic Phenotype of Factor V Leiden Carriers: Evidence from an Ex Vivo Model1
The impact of Syk-inhibition on 5B9 monoclonal HIT antibody-mediated procoagulant platelet formation1
Haemostaseological pearls1
Stable Factor IX Expression and Sustained Reductions in Factor IX Use 8 Years After Gene Therapy With CSL220 (Formerly AMT-060) in Adults with Hemophilia B [ENCORE]1
A patient with Klippel-Trénaunay-Syndrom and cerebral venous sinus thrombosis1
The Great Return: Rebuilding and Advancing the Swiss Haemophilia Registry1
Investigating the impact of oligogenic variation on severity of bleeding in hypofibrinogenemia1
Periinterventional management of edoxaban in major procedures: results from the DRESDEN NOAC REGISTRY1
Identification of key regulators of procoagulant COAT platelet generation by quantitative phosphoproteomic analysis and phosphoflow1
Global seroprevalence of neutralizing antibodies against adeno-associated virus (AAV) serotypes of relevance to gene therapy1
Safety and efficacy of recombinant Factor IX fusion protein (rIX-FP) in previously untreated patients with haemophilia B1
The effect of prophylactic corticosteroid treatment on adeno-associated virus-mediated gene therapy and potential mechanisms of action1
Investigation of Differential Interaction between GGCX and VKD Clotting Factors by an In Silico Approach1
Integration of Extracorporeal Membrane Oxygenation into the Management of High-Risk Pulmonary Embolism: An Overview of Current Evidence1
Digenic Inheritance of PROC and SERPINC1 Mutations Contributes to Multiple Sites Venous Thrombosis1
Identification of novel cryptic epitopes uncovers a distinct and consistent open ADAMTS13 conformation in iTTP1
Marker der Akute-Phase-Reaktion könnten Blutungen bei Hämophilie detektieren1
Determination of thrombotic risk in patients with antiphospholipid syndrome using a modified thrombin generation assay1
Residuale Venenokklusion nach längerer Antikoagulanzien-Therapie nicht mit erneuten venösen Thromboembolien assoziiert1
Treatment of Atypical Clots1
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Recombinant factor VIII binding to platelets influences fibrin clot formation and stability1
Diagnosis of Platelet Function Disorders: A Challenge for Laboratories1
Quantifying Residual Rivaroxaban Plasma Concentration after Antagonization with Andexanet Alfa: A Difficult Task in Routine Clinical Practice1
Role of Tissue Transglutaminase 2 in Fibrin Formation and Haemostasis1
Recurrent Venous Thromboembolism in Patients on Anticoagulation: An Update Based on the Revised AWMF S2k Guideline1
Die Gesellschaft für Thrombose- und Hämostaseforschung e.V. informiert0
Health-related quality-of-life outcomes 4 years after treatment with valoctocogene roxaparvovec0
Randomized-controlled cross-over pilot study on the effectiveness of manual lymphatic drainage in patients with hemophilic arthropathy0
Developing an assay to distinguish between HIT and VITT antibodies0
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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Challenging Situations in the Treatment of Cancer-Associated Thrombosis0
Implications of the API-CAT Trial for Extended Secondary Prophylaxis of Cancer-associated Venous Thromboembolism: Guidance from an Expert Panel0
Women's Health Issues in Thrombosis and Haemostasis0
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
Gut microbiota promotes arterial thrombus formation in hyperlipidemic Ldlr-/- mouse model0
In-vitro Evaluation of Anti-PEG Antibody Effects on the Activation of PEGylated Therapeutic FVIII and FIX Products0
Can German Health Insurance Claims Data Fill Information Gaps in Rare Chronic Diseases: Use Case of Haemophilia A0
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Characterization of patient-derived anti-PF4 antibodies in chemiluminescence assays0
Flow Chamber Analyses in Cardiovascular Research: Impact of Platelets and the Intercellular Crosstalk with Endothelial Cells, Leukocytes, and Red Blood Cells0
Thrombozytopenie: Sind Thrombozytentransfusionen vor Legen eines ZVK verzichtbar?0
Pitfalls in Coagulation Testing0
Thrombotic Ghost as a Complication of Anticoagulation Therapy: The Challenge of Anticoagulating Intracardiac Thrombi in Patients with Factor VII Deficiency0
Diagnosis and Therapy of Visceral Vein Thrombosis: An Update Based on the Revised AWMF S2k Guideline0
Venous thromboembolism therapy with edoxaban in daily - care patients: results from the DRESDEN NOAC REGISTRY0
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Hemostasis modification in the presence of concizumab combined with donors&apos; platelets, rFVIIa and/or tranexamic acid assessed by modified rotational thromboelastometry in patients with Glanzm0
VITT-like anti-PF4 antibodies need to be considered in patients with thrombocytopenia and thrombosis0
Disorders of Thrombosis and Hemostasis in Cancer0
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Molecular Genetics of Fletcher and Fitzgerald Traits0
The phenotypic and genetic assessment of hereditary antithrombin deficiency in 215 patients from the Rhein-Ruhr area in Germany0
Intrinsic Activated Thrombin Generation for Efficacy and Monitoring of Factor VIII Replacements and Mimetics0
Efficacy and safety of valoctocogene roxaparvovec 4 years after gene transfer in GENEr8-10
Indirect treatment comparisons of the gene therapy etranacogene dezaparvovec (CSL222) vs. extended half-life Factor IX therapies for severe or moderately severe hemophilia B0
Conformational opening of ADAMTS13 does not necessarily indicate preactivation of its metalloprotease domain0
Thrombozyten: Blutstillung ohne Gerinnselbildung0
Efficacy and safety of Mim8 prophylaxis in adults and adolescents with hemophilia A with or without inhibitors: Phase 3, open-label, randomized, controlled FRONTIER2 study0
Circulating Tumor Cells and Thromboembolic Events in Patients with Glioblastoma0
Laboratory Monitoring in Patients Receiving Emicizumab0
Aktueller Stand zur Reform der Gebührenordnung für Ärzte (GOÄ)0
Utility of ACMG classification to support interpretation of molecular genetic test results in patients with FVII deficiency0
Von Willebrand-disease_ a patient with a variant of uncertain significance: phenotype like type 1, genotype like type 30
Controlling Patient Multiple Electrode Aggregometry Results with Blood Samples of Blood Donors Improves Clinical Interpretation0
Evaluation of platelet parameters in pediatric oncology patients undergoing myelotoxic chemotherapy.0
Anti-Thrombin IgA in a Patient with Multiple Myeloma Leading to In Vitro Interference in Multiple Coagulation Tests and Confounding Diagnosis0
G-BA entscheidet Festgruppe für (plasmatischen) Blutgerinnungsfaktor VIII0
Expression and Release of Tumor Cell Tissue Factor Triggers Recurrent Thromboembolism in a Patient with Endometrial Cancer0
Paving the way to assay automation: Improving and simplifying VWF activity determination of VWF concentrates0
A hierarchical network of Src, Syk, Btk and PKC controls GPVI-dependent human platelet activation0
GPVI-mediated platelet activation aggravates inflammation and progressive aortic wall remodelling in abdominal aortic aneurysm formation0
Etranacogene dezaparvovec hemophilia B gene therapy phase 2b trial final results: stable and durable FIX level expression over 5 years [ENCORE]0
Double CRISPR/Cas9-knockout of ER chaperones, ERGIC transporters and GABARAPs reveal additive and dominant effect on FVIII secretion0
Grundlagen zur Anwendung von Andexanet0
Direct Oral Anticoagulants for Pulmonary Embolism0
Tackling the implementation hurdle: User-centric validation of a machine-learning decision support tool for the screening of mild bleeding disorders0
Understanding Congenital FXI Deficiency: Genetic Diagnosis and Correlation of Variant Detection Rate to Factor XI Activity0
Nachruf auf Rainer B. Zotz und Ankündigung der BDDH-Veranstaltung auf der GTH in Frankfurt 20230
TFPI deletion in myeloid cells exacerbates atherosclerotic plaque development0
Natural history of isolated distal deep vein thrombosis without anticoagulation. Prospective cohort under ultrasound surveillance0
Platelet hyperactivation and neutrophil extracellular traps promote thrombo-inflammation and glomerular endothelial dysfunction in diabetic kidney disease0
Platelet responsiveness in the post-acute phase of pulmonary embolism0
Aggregates of non-muscle myosin IIA in the erythrocytes associate with GATA1-related thrombocytopenia0
Erratum to: Congenital Fibrinogen Deficiencies: Not So Rare0
Relation of FVIII activity levels with global assays of hemostasis in persons with hemophilia A0
Detection of joint bleeding symptoms in Haemophilia with the Noraxon system – pilot study0
Oral Anticoagulation and Mortality in Cases with Intracranial Bleeding: Analysis of Nationwide Prescription and Hospitalization Data0
The Use of DOACs in Pediatrics: Current Therapeutic and Prophylactic Indications, Cardiac Indications, and Real-World Evidence—A Review0
In Contrast to Full-Length Factor VIII, the Calnexin (ER Chaperone) and LMAN1 (ERGIC transporter) Knockouts Have Minimal Effect on the Secretion of B-Domain-Deleted Factor VIII: Implication for Gene T0
The impact of enhanced platelet turnover on platelet reactivity in healthy humans0
A novel solid phase assay for the detection of fibrinolytic activities0
Sustained Efficacy of Marstacimab in Adults and Adolescents with Severe Hemophilia A or B without Inhibitors0
Marcumar-Intoxication: The Perils of Near-Homonyms0
Perioperative Management for Port Catheter Procedures in Pediatric Patients with Severe Hemophilia and Inhibitors0
Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia: a prospective validation study0
Platelets and Sera from Donors of Convalescent Plasma after Mild COVID-19 Show No Procoagulant Phenotype0
The effect of DNA methylation on inhibitor development in haemophilia A patients treated with FVIII concentrates0
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Analysis of the platelet activation profile in a novel experimental mouse model of AAA formation and progression0
Blutverlust bei Frauen im gebärfähigen Alter aufgrund oraler Antikoagulanzien gegen venöse Thromboembolien0
A Cross-sectional Analysis of Treatment in PUPs in 2021 in Germany – First Data from the GEPHARD Study Group0
Epithelial thrombin-PAR1 signaling and Nippostrongylus brasiliensis infection drive small intestinal villus vascularization0
A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia0
Post–Pulmonary Embolism Syndrome: An Update Based on the Revised AWMF-S2k Guideline0
Applicability of and adherence to anticoagulation-related standard-operating-procedures in standard surgical procedures – a single center quality control experience0
Joint health and physical activity in people with haemophilia A without factor VIII inhibitors before switching to emicizumab prophylaxis: Beyond ABR study interim analysis0
Type 2B von Willebrand Disease: Early Manifestation as Neonatal Thrombocytopenia0
Hypercoagulability combined with routine laboratory parameters accurately predicts liver cirrhosis decompensation0
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