Hämostaseologie is an interdisciplinary specialist journal on the complex topics of haemorrhages and thromboembolism and is aimed not only at haematologists, but also at a wide range of specialists from clinic and practice. The readership consequently includes both specialists for internal medicine as well as for surgical diseases.
Hämostaseologie是一本关于出血和血栓栓塞复杂主题的跨学科专业期刊，不仅面向血液学家，也面向来自临床和实践的广泛专家。因此，读者群包括内科和外科疾病的专家。
Role of Endothelial Cells in Acute and Chronic Thrombosis.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1675614
Lemierre Syndrome: Clinical Update and Protocol for a Systematic Review and Individual Patient Data Meta-analysis.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1654720
Management of Helicobacter pylori in Patients with Immune Thrombocytopenia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1683974
Pathophysiology of Autoimmune Thrombocytopenia: Current Insight with a Focus on Thrombopoiesis.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1678732
Laboratory Diagnostics in Thrombophilia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677840
Microvascular Thrombosis and Ischaemic Limb Losses in Critically Ill Patients.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1676823
Impact of Telemedicine Tools on Record Keeping and Compliance in Haemophilia Care.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1676128
The Role of Low Molecular Weight Heparins for Venous Thromboembolism Prevention in Medical Patients-What Is New in 2019?
来源期刊：HamostaseologieDOI：10.1055/s-0038-1677522
Causes and Secondary Prevention of Acute Ischemic Stroke in Adults.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1700502
Epidemiology and Clinical Manifestations of Immune Thrombocytopenia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1683416
Low-Molecular-Weight Heparin in Cancer Patients: Overview and Indications.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677796
Potential of Multidimensional, Large-scale Biodatabases to Elucidate Coagulation and Platelet Pathways as an Approach towards Precision Medicine in Thrombotic Disease.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1677520
Coagulation Signalling and Metabolic Disorders: Lessons Learned from Animal Models.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1688800
How Do We Treat Pregnancy-Related Venous Thromboembolism?
来源期刊：HamostaseologieDOI：10.1055/s-0039-1700501
MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1645840
First-Line Therapy for Immune Thrombocytopenia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1684031
Birth Control Pills and Thrombotic Risks: Differences of Contraception Methods with and without Estrogen.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677806
Prevalence of Obesity in Young Patients with Severe Haemophilia and Its Potential Impact on Factor VIII Consumption in Germany.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677874
Diagnosing Immune Thrombocytopenia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1678739
Trauma-Induced Coagulopathy.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677853
Smart Medication ™, an Electronic Diary for Surveillance of Haemophilia Home Care and Optimization of Resource Distribution.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1675575
Antibodies in the Treatment of Haemophilia A-A Biochemical Perspective.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1677521
Fulminant Essential Thrombocythemia Associated with Acquired Von Willebrand Syndrome and Bleeding Episodes in a 14-year-old Girl.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1679929
Therapie des Antiphospholipid-Syndroms (APS) mit DOAKs
来源期刊：HamostaseologieDOI：10.1055/s-0039-1694789
[Leitlinie der Gesellschaft für Thrombose- und Hämostaseforschung (GTH) zur Struktur- und Prozessqualität von Hämophilie-Zentren].
来源期刊：HamostaseologieDOI：10.1055/s-0039-1688450
Acquired Haemophilia A Associated with Subsequent Hepatocellular Carcinoma.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1668570
Immunomodulatory Second-Line Therapies for Immune Thrombocytopenia.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1684032
Long-Term Safety and Efficacy Data of a Plasma-Derived Factor VIII Concentrate with von Willebrand Factor for Treatment of Patients with Hemophilia A Covering 18 Years.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1698810
Child Abuse or Bleeding Disorder-An Interdisciplinary Approach.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677714
Current Trend of Invasive Orthopaedic Interventions for People with Haemophilia in Romania: Single Centre Experience.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1677884
Thrombopoietin Receptor Agonist Use for Immune Thrombocytopaenia.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1676129
Translational Research in Thrombosis and Haemostasis.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1691751
Replacement Therapy in Patients with Von Willebrand Disease-Indications and Monitoring.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1692688
Development of Haemophilia Treatment in the Eastern Part of Germany over the Last Decade in the Kompetenznetz Hämorrhagische Diathese Ost (KHDO).
来源期刊：HamostaseologieDOI：10.1055/s-0039-3399493
IWR-1 Inhibits Collagen-Induced Platelet Activation and Protects against Thrombogenesis.
来源期刊：HamostaseologieDOI：10.1055/s-0038-1676822
A Sardinian Family with Factor XI Deficiency.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1691752
Immune Thrombocytopenia-A Disease or a Group of Disorders? Where Do We Stand in 2019?
来源期刊：HamostaseologieDOI：10.1055/s-0039-1693660
A Retrospective Analysis of Clinical and Laboratory Data of Patients with Factor VII Deficiency: A Single Centre Experience.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1693425
A Prolonged Treatment Response in Acquired Von Willebrand Syndrome.
来源期刊：HamostaseologieDOI：10.1055/s-0039-1696960
