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Implications of the API-CAT Trial for Extended Secondary Prophylaxis of Cancer-associated Venous Thromboembolism: Guidance from an Expert Panel
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Outcome of Surgical Interventions in Patients with Haemophilia A and B Treated with Extended Half-Life (EHL) Factor Concentrates in a Single Centre
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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 Genotype
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Mitteilungen aus der Vorstandsarbeit
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Association Between Major Bleeding and In-Hospital Major Adverse Cardiovascular Events After Percutaneous Coronary Intervention in Acute Coronary Syndromes
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Sulodexid: Neue Hoffnung bei retinalen Gefäßerkrankungen
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Thrombosen bei malignen hämatologischen Erkrankungen: Risiko für Depressionen erhöht
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Stand GOÄ-Novelle, News zur ePA (elektronische Patientenakte), Ambulante Gentherapie für die Hämophilie B
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Performance Evaluation of Different FIX Activity Assays for Determining Nonacog Beta Pegol (N9-GP, Refixia®) Activity Using Reagent-/Platform-Specific Conversion Factors
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Erratum: “Diagnosis of Inherited Platelet Disorders”: Update of the Interdisciplinary S2k-Guideline [*] of the Permanent Pediatric Commission of the Society of Thrombosis and Haemostasis Research (GTH e.V.)
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Laboratory Monitoring in Patients Receiving Emicizumab
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The Timed Up and Go Test in Patients with Haemophilia: Assessing Reliability, Validity, and Predictive Variables
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Pharmazeutische Unternehmen außerhalb der USA unter Druck
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Blutverlust bei Frauen im gebärfähigen Alter aufgrund oraler Antikoagulanzien gegen venöse Thromboembolien
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Ungünstig veränderter Fibringerinnsel-Phänotyp bei Frauen nach postpartaler Blutung unbekannter Ursache: Einfluss niedriger Konzentration von Gerinnungsfaktoren
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Rare Congenital Bleeding Disorders – Challenges Remain
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Overview on Rare Congenital Bleeding Disorders and Epidemiological Data from the German Haemophilia Registry (DHR) and a Survey in Germany, Austria, and Switzerland
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Late Diagnosis of NBEAL2-related Gray Platelet Syndrome in Finnish Siblings with Lifelong Thrombocytopenia
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Usefulness of Global Coagulation Tests, Thrombin Generation and Viscoelastic Tests for Assessing the Bleeding Phenotype in Rare Coagulation Factor Deficiencies
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Understanding Congenital FXI Deficiency: Genetic Diagnosis and Correlation of Variant Detection Rate to Factor XI Activity
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Investigations on the Hemostatic Potential of Physiological Body Fluids
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Komplementdysregulation als Biomarker für Post Covid
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iTTP in der Schwangerschaft: Erfolgreiche Behandlung mit Caplacizumab
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Management of Adult Patients with Newly Diagnosed or Relapsed Primary Immune Thrombocytopenia in Eastern Austria
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Expert Opinion for Defining a Severe Bleeding Phenotype to Guide Prophylaxis in Patients with Nonsevere Hemophilia
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Challenging Situations in the Treatment of Cancer-Associated Thrombosis
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Leitlinie der Gesellschaft für Thrombose- und Hämostaseforschung (GTH) zur Struktur- und Prozessqualität von Hämophilie-Zentren
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From Code to Clots: Applying Machine Learning to Clinical Aspects of Venous Thromboembolism Prevention, Diagnosis, and Management
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Artificial Intelligence in Medicine: Are We Ready?
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Digital Technologies in Hereditary Coagulation Disorders: A Systematic Review
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