All Stories

  1. Editorial Compilation—Part XVIII
  2. External quality assessment for unfractionated heparin monitoring: An update from Australasia/Asia-Pacific
  3. Artificial intelligence and machine learning in thrombosis and hemostasis: a scoping review of clinical and laboratory applications, challenges, and future directions
  4. Welcome to Seminars in Thrombosis and Hemostasis 2026
  5. Diagnosing thrombophilia: the case for genetic or functional testing?
  6. Red Light Therapy in Thrombosis and Hemostasis
  7. A contemporary analysis of solid phase antiphospholipid antibody testing: implications for classification or diagnosis of antiphospholipid syndrome
  8. The increasing association of pulmonary embolism with cancer deaths: A seven-year, US-based, nationwide analysis
  9. Sustainable anticoagulation for climate resilient care
  10. “Alterations in visible light exposure modulate platelet function and regulate thrombus formation”: comment from Fan et al.
  11. Overview of laboratory diagnostics for immediate management of patients presenting to the emergency department with acute bleeding
  12. Acquired von Willebrand syndrome in children
  13. Clinical Significance of APTT Tests and Their Correlation with Heparin Anti-Xa and Anti-IIa Activities is Transformed by Pairing with a Heparin-Resistant Recalcification Solution (HRRS)
  14. Seminars in Thrombosis and Hemostasis: 2024 Impact Factor, Most Highly Cited Papers, and Other Journal Metrics
  15. Lupus Anticoagulant Testing for Diagnosis of Antiphospholipid Syndrome: A Perspective Informed by Local Practice
  16. A Review of Desmopressin Use in Bleeding Disorders: An Unsung Hero?
  17. Editorial Compilation—XVII
  18. Hemolysis detection accuracy on Stago sthemO 301
  19. An update on laboratory detection and interpretation of antiphospholipid antibodies for diagnosis of antiphospholipid syndrome: guidance from the ISTH-SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies: reply
  20. 2024 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  21. Oral Anticoagulation Therapy: An Update on Usage and Costs in the Endemic COVID-19 Era
  22. Comparative evaluation of routine coagulation testing on Stago sthemO 301 and Werfen ACL TOP 750
  23. Mortality from Pulmonary Embolism in Patients with Post-Coronavirus Disease Syndrome
  24. 2025 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  25. Nebulized Heparin in 2025: at the Interface between Promising Benefits and the Need for Further Research
  26. Factor Inhibitor Testing: An Update from Australasia/Asia-Pacific
  27. Manual tilt tube method for prothrombin time: a commentary on contemporary relevance
  28. Activated Protein C Resistance Testing: An Update From Australasia/Asia‐Pacific
  29. From errors to excellence: the pre-analytical journey to improved quality in diagnostics. A scoping review
  30. Laboratory Assessment of Factor VIII Inhibitors: When Is It Required? A Perspective Informed by Local Practice
  31. Current and emerging therapies as potential treatment for people with von Willebrand disease
  32. Innovative Diagnostic Solutions in Hemostasis
  33. Sticky Platelet Syndrome Revisited?
  34. An update on laboratory detection and interpretation of antiphospholipid antibodies for diagnosis of antiphospholipid syndrome: guidance from the ISTH-SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies
  35. Laboratory Testing for ADAMTS13 for Thrombotic Thrombocytopenia Purpura and Beyond
  36. Welcome to Seminars in Thrombosis and Hemostasis 2025: Toward the Next 50 Years of Publishing and Announcement of New Online Manuscript Submission System
  37. Innovative Diagnostic Solutions in Hemostasis
  38. Reflections on World Thrombosis Day 2024
  39. Revisiting the Environmental Impact of Inappropriate Clinical Laboratory Testing: A Comprehensive Overview of Sustainability, Economic, and Quality of Care Outcomes
  40. Reliability of generative artificial intelligence in identifying the major risk factors for venous thrombosis
  41. Routine Coagulation
  42. Erratum: Algorithm for Rapid Exclusion of Clinically Relevant Plasma Levels of Direct Oral Anticoagulants in Patients Using the DOAC Dipstick: An Expert Consensus Paper
  43. Heparin and Posttraumatic Stress Disorder
  44. New STH 2023 Impact Factor, Most Highly Cited Papers, and Other Journal Metrics
  45. Continued harmonization of the international normalized ratio across a large laboratory network: Evidence of sustained low interlaboratory variation and bias after a change in instrumentation
  46. EFLM Task Force Preparation of Labs for Emergencies (TF-PLE) recommendations for reinforcing cyber-security and managing cyber-attacks in medical laboratories
  47. EFLM Task Force Preparation of Labs for Emergencies (TF-PLE) survey on cybersecurity
  48. 2023 Eberhard F. Mammen Award Announcements: Part II–Young Investigator Awards
  49. COVID-19 vaccination prevents venous thrombosis in patients with SARS-CoV-2 infection and thereafter
  50. The Role of Viscoelastic Testing in Assessing Hemostasis: A Challenge to Standard Laboratory Assays?
  51. Should APTT become part of thrombophilia screening?
  52. Contact Activation: Where Thrombosis and Hemostasis Meet on a Foreign Surface, Plus a Mini-editorial Compilation (“Part XVI”)
  53. Prone Position and the Risk of Venous Thrombosis in COVID-19 Patients with Respiratory Failure
  54. Performance of direct oral anticoagulant (DOAC) testing by hemostasis laboratories: The Australasian/Asia‐Pacific experience
  55. The Most Highly Downloaded Publications from Seminars in Thrombosis and Hemostasis: A Data Analysis 10 Years in the Making
  56. Celebrating 50 Years of Seminars in Thrombosis and Hemostasis—Part IV
  57. Laboratory diagnosis of von Willebrand disease: the phenotype
  58. Editorial Compilation—XV
  59. 2024 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  60. Pearls and Pitfalls in the Measurement of Direct Oral Anticoagulants
  61. Variable Performance of D-dimer Testing by Hemostasis Laboratories: The Australasian/Asia-Pacific Experience
  62. D-dimer Levels for the exclusion of pulmonary embolism: making sense of international guideline recommendations
  63. Testing for the lupus anticoagulant: the good, the bad, and the ugly
  64. Venous Thrombosis in Airborne Viral Infections: Is Coronavirus Disease 2019 now Any Different from Influenza?
  65. Diagnostic value of D-dimer in differentiating multisystem inflammatory syndrome in Children (MIS-C) from Kawasaki disease: systematic literature review and meta-analysis
  66. Unfractionated heparin: optimizing laboratory monitoring and reducing unwanted interference in everyday hemostasis test practice
  67. Simplified Method for Removing Direct Oral Anticoagulant Interference in Mechanical Coagulation Test Systems—A Proof of Concept
  68. Algorithm for Rapid Exclusion of Clinically Relevant Plasma Levels of Direct Oral Anticoagulants in Patients Using the DOAC Dipstick: An Expert Consensus Paper
  69. Therapeutic drug monitoring of selected direct oral anticoagulants
  70. Artificial intelligence in the pre-analytical phase: State-of-the art and future perspectives
  71. D-dimer diagnostics: can I use any D-dimer assay? Bridging the knowledge-to-action gap
  72. Recent monthly mortality for pulmonary embolism in the US
  73. Vaccine-induced (immune) thrombotic thrombocytopenia (VITT): Diagnosis, guidelines, and reporting
  74. von Willebrand Disease
  75. Variable Performance of Lupus Anticoagulant Testing: The Australasian/Asia-Pacific Experience
  76. Description of an In Vitro Platelet Function Analyzer (PFA-100/PFA-200) 30 Years in the Making
  77. Classification Criteria for the Antiphospholipid Syndrome: Not the Same as Diagnostic Criteria for Antiphospholipid Syndrome
  78. The Most Highly Cited Publications from Seminars in Thrombosis and Hemostasis: A Data Analysis 50 Years in the Making
  79. Editorial Compilation XIV
  80. Effect of syringe underfilling on the quality of venous blood gas analysis
  81. Celebrating 50 Years of Seminars in Thrombosis and Hemostasis—Part III
  82. Welcome to Seminars in Thrombosis and Hemostasis 2024: 50 Years of Publishing
  83. New Seminars in Thrombosis and Hemostasis 2022 Impact Factor, Most Highly Cited Papers, and Other Journal Metrics
  84. Are Antiphospholipid Antibodies a Surrogate Risk Factor for Thrombosis in Sepsis?
  85. Incomplete filling of spray-dried K2EDTA evacuated blood tubes: impact on measuring routine hematological parameters on Sysmex XN-10
  86. Comparison of 2 ways of performing ristocetin-induced platelet agglutination mixing study for diagnosis of type 2B von Willebrand disease. Response to the publication of Soleimani et al
  87. Laboratory diagnosis of von Willebrand disease in the age of the new guidelines: considerations based on geography and resources
  88. Letter in response to Colpani et al “A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays”
  89. Results of the first survey of the EFLM Task Force Preparation of Labs for Emergencies (TF-PLE)
  90. Disruption of Laboratory Activities during the COVID-19 Pandemic: Results of an EFLM Task Force Preparation of Labs for Emergencies (TF-PLE) Survey
  91. Epidemiology and Predisposing Factors of Post-COVID Venous Thrombosis: A Concise Review
  92. Effects of Recombinant SARS-CoV-2 Spike Protein Variants on Platelet Morphology and Activation
  93. Incomplete filling of spray-dried K2EDTA evacuated blood tubes: impact on measuring routine hematological parameters on Sysmex XN-10
  94. Illustrated State-of-the-Art Capsules of the ISTH 2023 Congress
  95. 2022 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  96. A multicenter evaluation of the Technoscreen ADAMTS13 activity semi‐quantitative screening test for thrombotic thrombocytopenic purpura diagnosis and exclusion
  97. Reducing our carbon footprint in the haematology laboratory: A shared responsibility
  98. 2023 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  99. To Clot or Not to Clot: Is That the Question?
  100. Platelet-activating functional assay resolution in vaccine-induced immune thrombotic thrombocytopenia: differential alignment to PF4 ELISA platforms
  101. Mixing factor Xa and thrombin inhibiting direct oral anticoagulants produces a synergistic prolonging effect on most clotting tests
  102. The Role of the von Willebrand Factor Collagen-Binding Assay (VWF:CB) in the Diagnosis and Treatment of von Willebrand Disease (VWD) and Way Beyond: A Comprehensive 36-Year History
  103. Editorial Compilation—XIII
  104. Evolution of Hemostasis Testing: A Personal Reflection Covering over 40 Years of History*
  105. Pathology utilisation during COVID-19 outbreaks beyond viral testing: routine coagulation and D-dimer testing
  106. Mechanisms of Thrombosis in Heparin-Induced Thrombocytopenia and Vaccine-Induced Immune Thrombotic Thrombocytopenia
  107. Maintaining Hemostasis and Preventing Thrombosis in Coronavirus Disease 2019 (COVID-19)—Part IV
  108. Welcome to Seminars in Thrombosis & Hemostasis 2023
  109. Application of anti-Xa assay in monitoring unfractionated heparin therapy in contemporary antithrombotic management
  110. von Willebrand Disease: An Update on Diagnosis and Treatment
  111. An Overview of Laboratory Testing for ADAMTS13
  112. An Overview of Laboratory Testing for Antiphospholipid Antibodies
  113. Antiphospholipid Antibody Testing for Anti-cardiolipin and Anti-β2 Glycoprotein I Antibodies Using Chemiluminescence-Based Panels
  114. Auto-validation of Routine Coagulation/Hemostasis Assays with Reflex Testing of Abnormal Test Results
  115. Automated and Rapid ADAMTS13 Testing Using Chemiluminescence: Utility for Identification or Exclusion of TTP and Beyond
  116. Harmonization of Hemostasis Testing Across a Large Laboratory Network: An Example from Australia
  117. Hemostasis and Thrombosis: An Overview Focusing on Associated Laboratory Testing to Diagnose and Help Manage Related Disorders
  118. Heparin-Induced Thrombotic Thrombocytopenia (HITT) and Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT): Similar but Different
  119. Identification of ADAMTS13 Inhibitors in Acquired TTP
  120. Laboratory Testing for Activated Protein C Resistance (APCR): An Update
  121. Laboratory Testing for von Willebrand Disease Using a Composite Rapid 3-Test Chemiluminescence-Based von Willebrand Factor Assay Panel
  122. Laboratory Testing for von Willebrand Factor: Factor VIII Binding for the Diagnosis or Exclusion of Type 2N von Willebrand Disease: An Update
  123. Post-analytical Issues in Hemostasis and Thrombosis Testing: An Update
  124. Celebrating 50 Years of Seminars in Thrombosis and Hemostasis—Part II
  125. Assessment of immunological anti‐platelet factor 4 antibodies for vaccine‐induced thrombotic thrombocytopenia (VITT) in a large Australian cohort: A multicenter study comprising 1284 patients
  126. Corrigendum to “A multicentre assessment of contemporary laboratory assays for heparin induced thrombocytopenia” [Pathology (53) (2021) 247–256]
  127. How often are parenteral anticoagulants administered by parents?
  128. Autoimmune Diseases Affecting Hemostasis: A Narrative Review
  129. Dedication to Santa Maria Favaloro (1926–2022)
  130. The myths behind DOAC measurement: Analyses of prescribing information from different regulatory bodies and a call for harmonization
  131. Letter to the Editor: 10-Year Evolution in Worldwide Usage of Anticoagulant Drugs
  132. Toward 50 Years of Seminars in Thrombosis and Hemostasis
  133. Celebrating 50 Years of Seminars in Thrombosis and Hemostasis—Part I
  134. Strength of Anticoagulation in Moderate to Severe COVID-19 Illness: In Medio Stat Virtus?
  135. New Seminars in Thrombosis and Hemostasis (STH) 2021 Impact Factor, Most Highly Cited Papers, and Other Journal Metrics
  136. Laboratory Diagnosis of von Willebrand Disease (VWD): Geographical Perspectives
  137. Harmonizing factor assay-related testing performed in a large laboratory network
  138. Towards 50 years of platelet function analyser (PFA) testing
  139. D-dimer: old dogmas, new (COVID-19) tricks
  140. A Review of Autoimmune Acquired von Willebrand Factor Deficiency in Japan
  141. D-dimers—“Normal” Levels versus Elevated Levels Due to a Range of Conditions, Including “D-dimeritis,” Inflammation, Thromboembolism, Disseminated Intravascular Coagulation, and COVID-19
  142. Evaluating Performance of Contemporary and Historical von Willebrand Factor (VWF) Assays in the Laboratory Identification of von Willebrand Disease (VWD): The Australasian Experience
  143. Editorial Compilation XII
  144. Counting the carbon cost of heparin: an evolving tragedy of the commons?
  145. Getting smart with coagulation
  146. Harmonizing platelet function analyzer testing and reporting in a large laboratory network
  147. Heparin: The Journey from Parenteral Agent to Nasal Delivery
  148. 2022 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  149. A novel flow cytometry procoagulant assay for diagnosis of vaccine-induced immune thrombotic thrombocytopenia
  150. Complement Levels at Admission Reflecting Progression to Severe Acute Kidney Injury (AKI) in Coronavirus Disease 2019 (COVID-19): A Multicenter Prospective Cohort Study
  151. Cell-Free DNA, Neutrophil extracellular traps (NETs), and Endothelial Injury in Coronavirus Disease 2019– (COVID-19–) Associated Acute Kidney Injury
  152. “Von Willebrand disease type 2M: Correlation between genotype and phenotype”: Comment from Favaloro
  153. 2021 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  154. Evaluating errors in the laboratory identification of von Willebrand disease using contemporary von Willebrand factor assays
  155. Laboratory testing for platelet factor 4 antibodies: differential utility for diagnosis/exclusion of heparin induced thrombocytopenia versus suspected vaccine induced thrombotic thrombocytopenia
  156. Measurement of procoagulant platelets provides mechanistic insight and diagnostic potential in heparin‐induced thrombocytopenia
  157. The Intriguing Connections between von Willebrand Factor, ADAMTS13 and Cancer
  158. A multi‐laboratory assessment of lupus anticoagulant assays performed on the ACL TOP 50 family for harmonized testing in a large laboratory network
  159. Editorial Compilation XI
  160. The Benefits of Heparin Use in COVID-19: Pleiotropic Antiviral Activity beyond Anticoagulant and Anti-Inflammatory Properties
  161. An Analysis of the Sensitivity of the Activated Partial Thromboplastin Time (APTT) Assay, as Used in a Large Laboratory Network, to Coagulation Factor Deficiencies
  162. Maintaining Hemostasis and Preventing Thrombosis in Coronavirus Disease 2019 (COVID-19)—Part III
  163. Welcome to Seminars in Thrombosis & Hemostasis 2022
  164. Lupus anticoagulant testing during anticoagulation, including direct oral anticoagulants
  165. Should multiple factor dilutions be performed for all patient coagulation factor assays? Let the debate begin!
  166. Comparing the quality of testing for von Willebrand disease in different geographic localities
  167. Antibodies against Platelet Factor 4 and Their Associated Pathologies: From HIT/HITT to Spontaneous HIT-Like Syndrome, to COVID-19, to VITT/TTS
  168. Commentary on the ASH ISTH NHF WFH 2021 guidelines on the diagnosis of VWD: reflections based on recent contemporary test data
  169. What We Know (and Do not Know) Regarding the Pathogenesis of Pulmonary Thrombosis in COVID-19
  170. 2B von Willebrand disease diagnosis: Considerations reflecting on 2021 multisociety guidelines
  171. Review and evolution of guidelines for diagnosis of COVID-19 vaccine induced thrombotic thrombocytopenia (VITT)
  172. Guidance on the critical shortage of sodium citrate coagulation tubes for hemostasis testing
  173. The role of lipoprotein(a) in coronavirus disease 2019 (COVID-19) with relation to development of severe acute kidney injury
  174. Cerebral Venous Thrombosis Developing after COVID-19 Vaccination: VITT, VATT, TTS, and More
  175. Editorial Compilation X
  176. New STH (2020) Impact Factor, Most Highly Cited Papers, and Other Journal Metrics
  177. The Intriguing Relationships of von Willebrand Factor, ADAMTS13 and Cardiac Disease
  178. Why is Misdiagnosis of von Willebrand Disease Still Prevalent and How Can We Overcome It? A Focus on Clinical Considerations and Recommendations
  179. Harmonized D-dimer levels upon admission for prognosis of COVID-19 severity: Results from a Spanish multicenter registry (BIOCOVID-Spain study)
  180. Laboratory testing for suspected COVID‐19 vaccine–induced (immune) thrombotic thrombocytopenia
  181. COVID-19 and Antiphospholipid Antibodies: Time for a Reality Check?
  182. Is Lupus Anticoagulant a Significant Feature of COVID-19? A Critical Appraisal of the Literature
  183. Elevated soluble urokinase plasminogen activator receptor (suPAR) in COVID-19 patients
  184. A multi-laboratory assessment of congenital thrombophilia assays performed on the ACL TOP 50 family for harmonisation of thrombophilia testing in a large laboratory network
  185. Maintaining Hemostasis and Preventing Thrombosis in Coronavirus Disease 2019 (COVID-19): Part II
  186. Variability in D-dimer reporting revisited
  187. Laboratory testing for ADAMTS13: Utility for TTP diagnosis/exclusion and beyond
  188. The complicated relationships of heparin‐induced thrombocytopenia and platelet factor 4 antibodies with COVID‐19
  189. Verification of the ACL Top 50 Family (350, 550, and 750) for Harmonization of Routine Coagulation Assays in a Large Network of 60 Laboratories
  190. Mean Platelet Volume Predicts Severe COVID-19 Illness
  191. Increased VWF and Decreased ADAMTS-13 in COVID-19: Creating a Milieu for (Micro)Thrombosis
  192. 2021 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  193. Effect of sample heat inactivation on test levels of HIT-IgG(PF4-H) detected by the ACL AcuStar
  194. 2020 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  195. Heparin-induced thrombocytopenia: pathophysiology, diagnosis and treatment
  196. 2021 Update of the International Council for Standardization in Haematology Recommendations for Laboratory Measurement of Direct Oral Anticoagulants
  197. Machine learning and coagulation testing: the next big thing in hemostasis investigations?
  198. A multicenter laboratory assessment of a new automated chemiluminescent assay for ADAMTS13 activity
  199. A multicentre assessment of contemporary laboratory assays for heparin induced thrombocytopenia
  200. Editorial Compilation IX
  201. Welcome to Seminars in Thrombosis & Hemostasis 2021—New (2019) Impact Factor and Most Highly Cited Papers
  202. Circulating Levels of Tissue Plasminogen Activator and Plasminogen Activator Inhibitor-1 Are Independent Predictors of Coronavirus Disease 2019 Severity: A Prospective, Observational Study
  203. 2B or not 2B? A diagnosis of von Willebrand disease a lifetime of 86 years in the making
  204. Coronavirus Disease 2019–Associated Coagulopathy
  205. ADAMTS13 activity to von Willebrand factor antigen ratio predicts acute kidney injury in patients with COVID‐19: Evidence of SARS‐CoV‐2 induced secondary thrombotic microangiopathy
  206. Sample stability for routine coagulation testing
  207. D-dimer measurement in COVID-19: Silver bullet or clinical distraction?
  208. How we diagnose 2M von Willebrand disease (VWD): Use of a strategic algorithmic approach to distinguish 2M VWD from other VWD types
  209. Guidance from the Scientific and Standardization Committee for lupus anticoagulant/antiphospholipid antibodies of the International Society on Thrombosis and Haemostasis
  210. Oral anticoagulation therapy: an update on usage, costs and associated risks
  211. Maintaining Hemostasis and Preventing Thrombosis in Coronavirus Disease 2019 (COVID-19)—Part I
  212. Plasma vs serum as test sample for the chemiluminescent AcuStar HemosIL HIT‐IgG(PF4‐H) assay
  213. Standardization of Prothrombin Time/International Normalized Ratio (PT/INR)
  214. Periodontal Disease and Venous Thromboembolism
  215. Circulating Plasminogen Concentration at Admission in Patients with Coronavirus Disease 2019 (COVID-19)
  216. Hematology Laboratory Abnormalities in Patients with Coronavirus Disease 2019 (COVID-19)
  217. “Systematic review of viscoelastic testing (TEG/ROTEM) in obstetrics and recommendation from the women's SSC of the ISTH”: Response to comment from Kitchen et al
  218. Anticoagulant and antithrombotic therapy: globally applied according to local geographical selection criteria
  219. Novel approaches to ensuring quality in laboratory diagnostics and external quality assessment
  220. Statins and other drugs: Facing COVID-19 as a vascular disease
  221. The need for accurate D‐dimer reporting in COVID‐19: Communication from the ISTH SSC on fibrinolysis
  222. Classification of von Willebrand disease in the context of modern contemporary von Willebrand factor testing methodologies
  223. Hyperinflammation and derangement of renin-angiotensin-aldosterone system in COVID-19: A novel hypothesis for clinically suspected hypercoagulopathy and microvascular immunothrombosis
  224. Periodontitis, coronary heart disease and myocardial infarction: treat one, benefit all
  225. Navigating the Myriad of von Willebrand Factor Assays
  226. COVID-19 and Thrombotic or Thromboembolic Disease: Implications for Prevention, Antithrombotic Therapy, and Follow-Up
  227. 2020 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  228. Antisense lipoprotein[a] therapy: State-of-the-art and future perspectives
  229. Editorial Compilation VIII
  230. Gene therapy for hemophilias: the end of phenotypic testing or the start of a new era?
  231. The effect of DOACs on laboratory tests and their removal by activated carbon to limit interference in functional assays
  232. Pharmacological Agents Targeting Thromboinflammation in COVID-19: Review and Implications for Future Research
  233. Reporting of D-dimer data in COVID-19: some confusion and potential for misinformation
  234. COVID-19: progression of disease and intravascular coagulation – present status and future perspectives
  235. Mean platelet volume in arterial and venous thrombotic disorders
  236. D-dimer is Associated with Severity of Coronavirus Disease 2019: A Pooled Analysis
  237. Recommendations for Minimal Laboratory Testing Panels in Patients with COVID-19: Potential for Prognostic Monitoring
  238. Utility of the platelet function analyser (PFA-100/200) for exclusion or detection of von Willebrand disease: A study 22 years in the making
  239. Mixing studies for lupus anticoagulant: mostly yes, sometimes no
  240. Comparative assessment of von Willebrand factor multimers vs activity for von Willebrand disease using modern contemporary methodologies
  241. Laboratory testing for activated protein C resistance: rivaroxaban induced interference and a comparative evaluation of andexanet alfa and DOAC Stop to neutralise interference
  242. Impact of water temperature on reconstitution of quality controls for routine hemostasis testing
  243. Welcome to Seminars in Thrombosis and Hemostasis 2020—New (2018) Impact Factor and Most Highly Cited Papers
  244. Dental extractions on direct oral anticoagulants vs. warfarin: The DENTST study
  245. Unfractionated heparin monitoring with activated partial thromboplastin time
  246. Reducing the effect of DOAC interference in laboratory testing for factor VIII and factor IX: A comparative study using DOAC Stop and andexanet alfa to neutralize rivaroxaban effects
  247. Understanding the extent of the diagnostic potential of coagulation factors
  248. An Update on Biological and Clinical Associations between E-Cigarettes and Myocardial Infarction
  249. Direct Oral Anticoagulants for Disseminated Intravascular Coagulation: An Alliterative Wordplay or Potentially Valuable Therapeutic Interventions?
  250. Coagulation studies: achieving the right mix in a large laboratory network
  251. The Pointy End of Point-of-Care Testing for Direct Oral Anticoagulants
  252. Coagulation mixing studies: Utility, algorithmic strategies and limitations for lupus anticoagulant testing or follow up of abnormal coagulation tests
  253. International Council for Standardization in Haematology Recommendations for Hemostasis Critical Values, Tests, and Reporting
  254. Measurement of High-Sensitivity Cardiac Troponin in Pulmonary Embolism: Useful Test or a Clinical Distraction
  255. Drug-Induced Thrombocytopenia: Mechanisms and Laboratory Diagnostics
  256. Platelet Transfusion Thresholds: How Low Can We Go in Respect to Platelet Counting?
  257. Semi‐automated von Willebrand factor multimer assay for von Willebrand disease: Further validation, benefits and limitations
  258. A diagnosis of von Willebrand disease despite normal test results for factor VIII and von Willebrand factor antigen and activity
  259. The Russell viper venom time (RVVT) test for investigation of lupus anticoagulant (LA)
  260. The Model List of Essential In Vitro Diagnostics: nuisance or opportunity?
  261. Understanding the “philosophy” of laboratory hemostasis
  262. Genetic Testing for Thrombophilia-Related Genes: Observations of Testing Patterns for Factor V Leiden (G1691A) and Prothrombin Gene “Mutation” (G20210A)
  263. Neutralising rivaroxaban induced interference in laboratory testing for lupus anticoagulant (LA): A comparative study using DOAC Stop and andexanet alfa
  264. Development and implementation of an expert rule set for automated reflex testing and validation of routine coagulation tests in a large pathology network
  265. Editorial Compilation VII
  266. Current and Emerging Direct Oral Anticoagulants: State-of-the-Art
  267. Diagnosis and management of heparin‐induced thrombocytopenia: a consensus statement from the Thrombosis and Haemostasis Society of Australia and New ZealandHITWriting Group
  268. Statins for Preventing Venous Thrombosis: For or Against?
  269. Vascular Disease and Dementia: Lipoprotein(a) as a Neglected Link
  270. Impact of low volume citrate tubes on results of first‐line hemostasis testing
  271. Influence of hypertriglyceridemia, hyperbilirubinemia and hemolysis on thrombin generation in human plasma
  272. 2019 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  273. Laboratory testing for lupus anticoagulant (LA) in patients taking direct oral anticoagulants (DOACs): potential for false positives and false negatives
  274. Thrombin generation in different commercial sodium citrate blood tubes
  275. Recent Advances in Mainstream Hemostasis Diagnostics and Coagulation Testing
  276. 2018 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  277. To Maintain or Cease Non–Vitamin K Antagonist Oral Anticoagulants Prior to Minimal Bleeding Risk Procedures: A Review of Evidence and Recommendations
  278. Analytical Assessment of the New Roche Cobas t 711 Fully Automated Coagulation Analyzer
  279. Editorial Compilation VI
  280. Welcome to Seminars in Thrombosis and Hemostasis 2019–New (2017) Impact Factor and Most Highly Cited Papers
  281. Commentary: Controversies in Thrombosis and Hemostasis Part 2–Does Sticky Platelet Syndrome Exist?
  282. How to Optimize Activated Partial Thromboplastin Time (APTT) Testing: Solutions to Establishing and Verifying Normal Reference Intervals and Assessing APTT Reagents for Sensitivity to Heparin, Lupus Anticoagulant, and Clotting Factors
  283. Emicizumab (ACE910): Clinical background and laboratory assessment of hemophilia A
  284. Lessons learnt from local real‐life experience with idarucizumab for the reversal of dabigatran
  285. Analytical performance of the new D‐dimer and antithrombin assay on Roche cobas t 711 analyzer
  286. Dark chocolate modulates platelet function with a mechanism mediated by flavan-3-ol metabolites
  287. Danger of false negative (exclusion) or false positive (diagnosis) for ‘congenital thrombophilia’ in the age of anticoagulants
  288. Harms and Benefits of Using Aspirin for Primary Prevention of Cardiovascular Disease: A Narrative Overview
  289. Anticoagulation at the extremes of body weight: choices and dosing
  290. Rare forms of von Willebrand disease
  291. e-thrombosis: epidemiology, physiopathology and rationale for preventing computer-related thrombosis
  292. How to Generate a More Accurate Laboratory-Based International Normalized Ratio: Solutions to Obtaining or Verifying the Mean Normal Prothrombin Time and International Sensitivity Index
  293. Prothrombotic State Induced by Middle-Distance Endurance Exercise in Middle-Aged Athletes
  294. Postanalytical considerations that may improve the diagnosis or exclusion of haemophilia and von Willebrand disease
  295. Laboratory hemostasis: from biology to the bench
  296. 45 years of Seminars in Thrombosis and Hemostasis
  297. Myocardial Infarction, Unstable Angina, and White Thrombi: Time to Move Forward?
  298. Sudden Cardiac and Noncardiac Death in Sports: Epidemiology, Causes, Pathogenesis, and Prevention
  299. A 2018 Update on the Editorial and Publication Policy of Seminars in Thrombosis and Hemostasis
  300. Differential sensitivity of von Willebrand factor activity assays to reduced VWF molecular weight forms: A large international cross-laboratory study
  301. HIT or miss? A comprehensive contemporary investigation of laboratory tests for heparin induced thrombocytopenia
  302. Mathematical rounding as a post-analytical issue in pathology reporting: generation of bias in INR resulting
  303. An update on quality control for the PFA-100/PFA-200
  304. Car Travel-Related Thrombosis: Fact or Fiction?
  305. Not as sweet as honey: A rare case of an apparent factor V “inhibitor” in association with bee sting anaphylaxis
  306. Recent initiatives in harmonization of hemostasis practice
  307. On the complexity of hemostasis and the need for harmonization of test practice
  308. Towards harmonization of external quality assessment/proficiency testing in hemostasis
  309. Management of pregnancy complications in type 2N von Willebrand disease associated to a novel mutation
  310. 2018 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  311. Editorial Compilation V
  312. 2017 Eberhard F. Mammen Award Announcements: Part II–Young Investigator Awards
  313. International Council for Standardization in Haematology (ICSH) Recommendations for Laboratory Measurement of Direct Oral Anticoagulants
  314. Welcome to Seminars in Thrombosis & Hemostasis 2018. New (2016) Impact Factor and Most Highly Cited Papers
  315. Assessment of Plasma Sample Quality on Siemens Atellica COAG 360 System
  316. von Willebrand Disease
  317. von Willebrand Disease
  318. Lack of grading agreement among international hemostasis external quality assessment programs
  319. Preanalytical issues that may cause misdiagnosis in haemophilia and von Willebrand disease
  320. Commentary: Controversies in Thrombosis and Hemostasis Part 1—Hematidrosis: “Blood, Sweat and Fears” or A “Pigment of Fertile Imaginations?”
  321. Laboratory tests for identification or exclusion of heparin induced thrombocytopenia: HIT or miss?
  322. Time dependent reduction in platelet aggregation using the multiplate analyser and hirudin blood due to platelet clumping
  323. Trenonacog alfa for prophylaxis, on-demand and perioperative management of hemophilia B
  324. The increasing maturity of the von Willebrand factor collagen binding in von Willebrand disease diagnosis
  325. Replacing warfarin therapy with the newer direct oral anticoagulants, or simply a growth in anticoagulation therapy? Implications for pathology testing
  326. Venous and Arterial Thromboses: Two Sides of the Same Coin?
  327. Laboratory Monitoring or Measurement of Direct Oral Anticoagulants (DOACs): Advantages, Limitations and Future Challenges
  328. Gender related issues in thrombosis and hemostasis
  329. Editorial Compilation IV
  330. Direct oral anticoagulants: analysis of worldwide use and popularity using Google Trends
  331. Potential misdiagnosis of von Willebrand disease and haemophilia caused by ineffective mixing of thawed plasma
  332. Managing the patient identification crisis in healthcare and laboratory medicine
  333. Therapeutic monitoring of unfractionated heparin – trials and tribulations
  334. Novel (Oral) Anticoagulant Challenges in Surgery
  335. Serum Concentration of Growth Differentiation Factor-15 Is Independently Associated with Global Platelet Function and Higher Fibrinogen Values in Adult Healthy Subjects
  336. Clinical and laboratory diagnosis of heparin induced thrombocytopenia: an update
  337. 2017 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  338. Evaluation of a new commercial von Willebrand factor multimer assay
  339. 2B or not 2B? A prothrombotic tendency masquerading as a bleeding disorder
  340. Translational aspects of developmental hemostasis: infants and children are not miniature adults and even adults may be different
  341. Impact of experimental hypercalcemia on routine haemostasis testing
  342. 2016 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  343. The Intriguing Link between the Intestinal Microbiota and Cardiovascular Disease
  344. Platelet function testing in pediatric patients
  345. Emerging treatments for hemophilia: patients and their treaters spoilt for choice, but laboratories face a difficult path?
  346. Welcome to Seminars in Thrombosis & Hemostasis 2017 — New (2015) Impact Factor and Most Highly Cited Papers
  347. Editorial Compilation III
  348. Critical laboratory values in hemostasis: toward consensus
  349. Clinical utility of closure times using the platelet function analyzer‐100/200
  350. Explaining and reducing the variation in inter-laboratory reported values for International Normalised Ratio
  351. Exploring the iceberg of inappropriateness in hemostasis testing
  352. Diagnosis or Exclusion of von Willebrand Disease Using Laboratory Testing
  353. Laboratory Testing for von Willebrand Factor: Factor VIII Binding (for 2N VWD)
  354. Laboratory Testing for von Willebrand Factor Ristocetin Cofactor (VWF:RCo)
  355. Laboratory Testing for Activated Protein C Resistance (APCR)
  356. Laboratory Testing for Von Willebrand Factor Multimers
  357. Laboratory Testing for von Willebrand Factor Antigen (VWF:Ag)
  358. Laboratory Testing for von Willebrand Factor Collagen Binding (VWF:CB)
  359. Laboratory Testing for von Willebrand Factor Activity by Glycoprotein Ib Binding Assays (VWF:GPIb)
  360. Laboratory Testing Protocols for Heparin-Induced Thrombocytopenia (HIT) Testing
  361. Optimizing the Verification of Mean Normal Prothrombin Time (MNPT) and International Sensitivity Index (ISI) for Accurate Conversion of Prothrombin Time (PT) to International Normalized Ratio (INR)
  362. Overview of Hemostasis and Thrombosis and Contribution of Laboratory Testing to Diagnosis and Management of Hemostasis and Thrombosis Disorders
  363. Platelet Function Analyzed by Light Transmission Aggregometry
  364. Preanalytical Issues in Hemostasis and Thrombosis Testing
  365. Ristocetin-Induced Platelet Aggregation (RIPA) and RIPA Mixing Studies
  366. Laboratory monitoring of direct oral anticoagulants (DOACs)—The perfect storm?
  367. D-Dimer Testing: Laboratory Aspects and Current Issues
  368. Post-analytical Issues in Hemostasis and Thrombosis Testing
  369. Critical pre-examination variables in the hemostasis laboratory and their quality indicators
  370. Mixing of thawed coagulation samples prior to testing: Is any technique better than another?
  371. Troubleshooting an isolate prolongation of activated partial thromboplastin time in a patient with acute myocardial infarction—a paradigmatic case report
  372. Utility of the von Willebrand factor collagen binding assay in the diagnosis of von Willebrand disease
  373. Giuseppe (Joseph) Favaloro (1922–2016)
  374. Editorial Compilation—II
  375. Monitoring Therapy during Treatment of von Willebrand Disease
  376. Laboratory tests used to help diagnose von Willebrand disease: an update
  377. Andexanet: Effectively Reversing Anticoagulation
  378. Characterizing the Mechanistic Pathways of the Instant Blood-Mediated Inflammatory Reaction in Xenogeneic Neonatal Islet Cell Transplantation
  379. Type 2M and Type 2A von Willebrand Disease: Similar but Different
  380. 2016 Eberhard F. Mammen Award Announcements: Part I — Most Popular Articles
  381. Evaluation of a von Willebrand factor three test panel and chemiluminescent-based assay system for identification of, and therapy monitoring in, von Willebrand disease
  382. Diagnostics of Inherited Bleeding Disorders of Secondary Hemostasis: An Easy Guide for Routine Clinical Laboratories
  383. Human plasma-derived FVIII/VWD concentrate (Biostate): a review of experimental and clinical pharmacokinetic, efficacy and safety data
  384. Type 2M von Willebrand disease - more often misidentified than correctly identified
  385. Why Do Patients Bleed?
  386. Editorial Compilation I
  387. Welcome to Seminars in Thrombosis & Hemostasis 2016: New (2014) Impact Factor and Most Highly Cited Articles
  388. Treatment of von Willebrand Disease
  389. Harmonizing the International Normalized Ratio (INR)
  390. Platelet type von Willebrand disease and registry report: communication from the SSC of the ISTH
  391. Hereditary Thrombophilias: Pathophysiology, Timing of Testing and Familial Testing
  392. Harmonisation of D-dimer — A call for action
  393. The effect of the direct factor Xa inhibitors apixaban and rivaroxaban on haemostasis tests: a comprehensive assessment using in vitro and ex vivo samples
  394. Allergy and Venous Thromboembolism: A Casual or Causative Association
  395. 2015 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  396. 2015 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  397. Influence of posture on routine hemostasis testing
  398. “Bleeding in the jungle”
  399. Toward improved diagnosis of HIT
  400. Recent advances in laboratory-aided diagnosis of von Willebrand disease
  401. Effect of contaminant 0.9% saline on tests of haemostasis
  402. Commentary
  403. Determining the stability of complete blood count parameters in stored blood samples using the SYSMEX XE-5000 automated haematology analyser
  404. Hot Topics VII
  405. Laboratory monitoring of warfarin in the era of direct oral anticoagulants
  406. The effect of dabigatran on haemostasis tests: a comprehensive assessment using in vitro and ex vivo samples
  407. The Platelet Function Analyser (PFA)-100 and von Willebrand disease: a story well over 16 years in the making
  408. Pearls and pitfalls in factor inhibitor assays
  409. Detection of mild inherited disorders of blood coagulation: current options and personal recommendations
  410. Newer Hemostatic Agents
  411. Quality in Hemostasis and Thrombosis — Part IV
  412. Diagnostics in Venous Thromboembolism: From Origin to Future Prospects
  413. International Normalized Ratio Monitoring of Vitamin K Antagonist Therapy: Comparative Performance of Point-of-Care and Laboratory-Derived Testing
  414. International Survey on D-Dimer Test Reporting: A Call for Standardization
  415. Anticoagulant Therapy: Present and Future
  416. The Changing Face of Hemostasis Testing in Modern Laboratories: Consolidation, Automation, and Beyond
  417. Laboratory Testing in the Era of Direct or Non–Vitamin K Antagonist Oral Anticoagulants: A Practical Guide to Measuring Their Activity and Avoiding Diagnostic Errors
  418. Next Generation Antithrombotic Therapy: Focus on Antisense Therapy against Coagulation Factor XI
  419. Welcome to Seminars in Thrombosis & Hemostasis 2015: New (2013) Impact Factor and Most Highly Cited Articles
  420. Reflections on the next generation of hemostasis instrumentation. A glimpse into the future?
  421. Recent guidelines and recommendations for laboratory assessment of the direct oral anticoagulants (DOACs): is there consensus?
  422. The new and the old of heparin-induced thrombocytopenia
  423. The effect of hyperglycaemia on haemostasis testing - a volunteer study
  424. Towards improved diagnosis of von Willebrand disease: Comparative evaluations of several automated von Willebrand factor antigen and activity assays
  425. Evaluating the interaction of von Willebrand factor and ADAMTS13 - and perhaps also beyond ADAMTS13
  426. Urgent monitoring of dabigatran plasma levels: sometimes less is more
  427. Dedication
  428. Articles from Seminars in Thrombosis & Hemostasis (STH) Archives: Part II
  429. A Short History of Thrombosis and Hemostasis: Part II (40th Year Celebratory Issue)
  430. Hot Topics VI
  431. 2014 Eberhard F. Mammen Award Announcements: Part II—Young Investigator Awards
  432. Dangers in the Practice of Defensive Medicine in Hemostasis Testing for Investigation of Bleeding or Thrombosis: Part I—Routine Coagulation Testing
  433. Sodium citrate blood contamination by K2-ethylenediaminetetraacetic acid (EDTA): impact on routine coagulation testing
  434. Antiphospholipid antibody testing for the antiphospholipid syndrome: a comprehensive practical review including a synopsis of challenges and recent guidelines
  435. Thrombophilia testing in patients taking direct oral anticoagulants. Handle with care
  436. A Review of the Value of D-dimer Testing for Prediction of Recurrent Venous Thromboembolism with Increasing Age
  437. Aging Hemostasis: Changes to Laboratory Markers of Hemostasis As We Age—A Narrative Review
  438. Evaluating errors in the laboratory identification of von Willebrand disease in the real world
  439. Comparative sensitivity of commercially available aPTT reagents to mulga snake (Pseudechis australis) venom
  440. A Short History of Thrombosis and Hemostasis: Part I (40th Year Celebratory Issue)
  441. Articles from Seminars in Thrombosis & Hemostasis (STH) Archives
  442. Diagnosing von Willebrand Disease: A Short History of Laboratory Milestones and Innovations, Plus Current Status, Challenges, and Solutions
  443. Combined Administration of Antibiotics and Direct Oral Anticoagulants: A Renewed Indication for Laboratory Monitoring?
  444. Response to “Comment on E-Cigarettes and Cardiovascular Risk: Beyond Science and Mysticism”
  445. 2014 Eberhard F. Mammen Award Announcements: Part I—Most Popular Articles
  446. Laboratory testing for factor inhibitors
  447. von Willebrand disease and platelet disorders
  448. Interference from heterophilic antibodies in D-dimer assessment. A case report
  449. Influence of centrifuge brake on residual platelet count and routine coagulation tests in citrated plasma
  450. Artefactual “in-vitro coagulopathy” in a patient with non-Hodgkin lymphoma and lower gastrointestinal bleeding
  451. Quality in Hemostasis and Thrombosis — Part III
  452. Standardization and Harmonization of Antiphospholipid Antibody Assays
  453. External Quality Assessment/Proficiency Testing and Internal Quality Control for the PFA-100 and PFA-200: An Update
  454. A Tribute to Professor Jerry Koutts, MD (Syd), BS, FRACP, FRCPA (1944–2013)
  455. Welcome to Seminars in Thrombosis & Hemostasis 2014
  456. Hot Topics V
  457. Technological Advances in the Hemostasis Laboratory
  458. The futility of thrombophilia testing
  459. von Willebrand Disease
  460. E-Cigarettes and Cardiovascular Risk: Beyond Science and Mysticism
  461. Problems and Solutions in Laboratory Testing for Hemophilia
  462. Editorial
  463. Technical Evaluation of the Novel Preanalytical Module on Instrumentation Laboratory ACL TOP: Advancing Automation in Hemostasis Testing
  464. Problems and Solutions in Laboratory Testing for Hemophilia
  465. Influence of Residual Platelet Count on Routine Coagulation, Factor VIII, and Factor IX Testing in Postfreeze-Thaw Samples
  466. Sample collection and platelet function testing
  467. Lupus anticoagulant testing – sometimes mixing is required
  468. Still more discussion on the journal impact factor
  469. 2013 Eberhard F. Mammen Award Announcements
  470. Laboratory testing for the new oral anticoagulants: a review of current practice
  471. Venous Thrombosis Associated with HMG-CoA Reductase Inhibitors
  472. Variability and diagnostic utility of antiphospholipid antibodies including lupus anticoagulants
  473. Quality in Hemostasis and Thrombosis, Part II
  474. Regulation in Hemostasis and Thrombosis: Part I—In Vitro Diagnostics
  475. Laboratory Evaluation of Von Willebrand Disease: Phenotypic Analysis
  476. Causes of Errors in Medical Laboratories
  477. External Quality Assessment of Factor VIII Inhibitor Assays
  478. Hot Topics IV
  479. Trials and tribulations in lupus anticoagulant testing
  480. Article downloads and citations: Is there any relationship?
  481. Welcome to Seminars in Thrombosis & Hemostasis 2013
  482. Interference in Coagulation Testing: Focus on Spurious Hemolysis, Icterus, and Lipemia
  483. Time for a conceptual shift in assessment of internal quality control for whole blood or cell-based testing systems? An evaluation using platelet function and the PFA-100 as a case example
  484. Establishment and characterization of a new and stable collagen‐binding assay for the assessment of von Willebrand factor activity
  485. Massive Posttraumatic Bleeding: Epidemiology, Causes, Clinical Features, and Therapeutic Management
  486. Novel and Emerging Therapies: Thrombus-Targeted Fibrinolysis
  487. Quality in Hemostasis and Thrombosis—Part I
  488. Discard tube for coagulation testing
  489. New developments in the diagnosis and treatment of von Willebrand disease
  490. ABO blood group, hypercoagulability, and cardiovascular and cancer risk
  491. Laboratory hemostasis: milestones in Clinical Chemistry and Laboratory Medicine
  492. In Vitro and In Vivo Hemolysis
  493. Thrombotic and Hemorrhagic Syndromes Associated with Autoimmunity and Infection
  494. 2012 Eberhard F. Mammen Award Announcements
  495. Different bleeding risk in type 2A and 2M von Willebrand disease: a 2‐year prospective study in 107 patients: a rebuttal
  496. External Quality Assurance for Heparin Monitoring
  497. Acquired Inhibitors of Coagulation Factors: Part I—Acquired Hemophilia A
  498. Acquired Inhibitors of Coagulation Factors: Part II
  499. Acquired Functional Coagulation Inhibitors: Review on Epidemiology, Results of a Wet-Workshop on Laboratory Detection, and Implications for Quality of Inhibitor Diagnosis
  500. Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders
  501. Quality Standards for Sample Processing, Transportation, and Storage in Hemostasis Testing
  502. Quality Standards for Sample Collection in Coagulation Testing
  503. Patient Safety and Quality in Laboratory and Hemostasis Testing: A Renewed Loop?
  504. Laboratory identification of factor inhibitors: an update
  505. Differential sensitivity of von Willebrand factor (VWF) ‘activity’ assays to large and small VWF molecular weight forms: a cross‐laboratory study comparing ristocetin cofactor, collagen‐binding and mAb‐based assays
  506. Paradoxical thrombosis part 1: factor replacement therapy, inherited clotting factor deficiencies and prolonged APTT
  507. Paradoxical thrombosis, part 2: anticoagulant and antiplatelet therapy
  508. The Antiphospholipid Syndrome: Diagnosis, Pathogenesis, Laboratory Testing, and Management
  509. Internal Quality Control and External Quality Assurance in Testing for Antiphospholipid Antibodies: Part I—Anticardiolipin and Anti-β2-Glycoprotein I Antibodies
  510. Internal Quality Control and External Quality Assurance in Testing for Antiphospholipid Antibodies: Part II—Lupus Anticoagulant
  511. Diagnosis of von Willebrand Disease
  512. Evaluating laboratory approaches to the identification of lupus anticoagulants: A diagnostic challenge from the RCPA Haematology QAP
  513. Relationship between short activated partial thromboplastin times, thrombin generation, procoagulant factors and procoagulant phospholipid activity
  514. Clinical audit of antiphospholipid antibody testing in tertiary practice: towards improved relevance in thrombophilia investigations
  515. Biological therapies for von Willebrand disease
  516. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations, Part VI
  517. Coffee Intake and Cardiovascular Disease: Virtue Does Not Take Center Stage
  518. Hemostatic Properties of the Lymph: Relationships with Occlusion and Thrombosis
  519. Hot Topics III
  520. Welcome to Seminars in Thrombosis & Hemostasis 2012
  521. 2B or not 2B? Masquerading as von Willebrand disease?
  522. Pre-analytical Variables in Coagulation Testing Associated With Diagnostic Errors in Hemostasis
  523. The new oral anticoagulants and the future of haemostasis laboratory testing
  524. Proficiency testing/external quality assurance for the PFA-100®
  525. Influence of mechanical trauma of blood and hemolysis on PFA-100 testing
  526. Biomedical research platforms and their influence on article submissions and journal rankings: An update
  527. Standards and reference materials for the anticardiolipin and anti-β2glycoprotein I assays: A report of recommendations from the APL Task Force at the 13th International Congress on Antiphospholipid Antibodies
  528. A novel flow cytometry single tube bead assay for quantitation of von Willebrand factor antigen and collagen-binding
  529. International consensus guidelines on anticardiolipin and anti–β 2 ‐glycoprotein I testing: Report from the 13th International Congress on Antiphospholipid Antibodies
  530. Antisense therapy in the treatment of hypercholesterolemia
  531. Laboratory testing of anticoagulants: the present and the future
  532. A robust method for testing urinary iodine using a microtitre robotic system
  533. Iodine Deficiency: Current Aspects and Future Prospects
  534. Direct-to-consumer testing: more risks than opportunities
  535. Holiday Thrombosis
  536. Seminars in Thrombosis & Hemostasis 2010: Impact Factor and Highest-Cited Articles from 2008 to 2009
  537. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations. Part V.
  538. Diagnosis and classification of von Willebrand disease
  539. von Willebrand Factor Assay Proficiency Testing Continued
  540. Thrombocytopenic Platelet Disorders
  541. Diagnosis of type 1 vs. 2A and 2M von Willebrand disease
  542. Cycling: To Race or to Live – Reflections on Skewed Priorities?
  543. Distinguishing types 1 and 2M von Willebrand disease
  544. Diagnosis and Management of v on Willebrand Disease in Australia
  545. von Willebrand Disease: Local Diagnosis and Management of a Globally Distributed Bleeding Disorder
  546. 2011 Eberhard F. Mammen Award Announcements
  547. Michael Dawson, B. Pharm. (Hon), Ph.D. (1954–2010)
  548. v on Willebrand Disease: Local Diagnosis and Management of a Globally Distributed Bleeding Disorder
  549. Assessment for antithrombin deficiency in the real world
  550. Regulation of in vitro diagnostics (IVDs) for use in Australian pathology laboratories: a gloomy outlook for future pathology testing in this country?
  551. Inherited disorders of blood coagulation
  552. Laboratory testing and/or monitoring of the new oral anticoagulants/antithrombotics: for and against?
  553. Laboratory diagnostics and appropriate care of people with haemophilia
  554. Inherited and acquired factor V deficiency
  555. A clinical audit of congenital thrombophilia investigation in tertiary practice
  556. External quality assurance for the PFA‐100®
  557. Prevention of Venous Thromboembolism: Focus on Mechanical Prophylaxis
  558. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations, Part IV
  559. Obstructive Sleep Apnea Syndrome and Cardiovascular Diseases
  560. Laboratory Diagnosis of von Willebrand Disease: The Phenotype
  561. Frequency of Platelet type versus Type 2B von Willebrand Disease
  562. Venous Thromboembolism in Chronic Liver Disease
  563. Glycoprotein IIb/IIIa inhibitors: an update on the mechanism of action and use of functional testing methods to assess antiplatelet efficacy
  564. Functional analysis of three recombinant A1-VWF domain mutants in comparison to wild type and plasma-derived VWF facilitates subtyping in type 2 von Willebrand disease
  565. ‘Criteria’ aPL tests: Report of a Task Force and preconference workshop at the 13th International Congress on Antiphospholipid Antibodies, Galveston, Texas, April 2010
  566. More on preanalytical variables affecting platelet function testing using light transmittance aggregometry
  567. Laboratory testing for the antiphospholipid syndrome: making sense of antiphospholipid antibody assays
  568. Hormones, Endocrine Disorders, and Hemostasis
  569. The Spectrum of Coagulation Abnormalities in Thyroid Disorders
  570. Rethinking the diagnosis of von Willebrand disease
  571. Coagulation update: What's new in hemostasis testing?
  572. Regulation of in vitro diagnostics (IVDs) for use in clinical diagnostic laboratories: towards the light or dark in clinical laboratory testing?
  573. Interaction of factor VIII and von Willebrand factor and the identification of type 2N von Willebrand disease
  574. Studies on in vitro hemolysis and utility of corrective formulas for reporting results on hemolyzed specimens
  575. Laboratory diagnosis of von Willebrand disease: results from a prospective and blind study in 32 laboratories worldwide using lyophilized plasmas
  576. Laboratory investigation of lupus anticoagulants: mixing studies are sometimes required
  577. Validation of improved performance characteristics for the automated von Willebrand factor ristocetin cofactor activity assay
  578. Farewell to 2010!
  579. Discard Tubes Are Sometimes Necessary When Drawing Samples for HemostasisThe Authors’ Reply
  580. Global Hemostasis: New Approaches to Patient Diagnosis and Treatment Monitoring
  581. Winners of the 2010 Eberhard F. Mammen Award for Most Popular Article during 2008–2009
  582. Hemolytic Uremic Syndrome
  583. C-reactive protein and venous thromboembolism: causal or casual association?
  584. Recombinants in Thrombosis and Hemostasis: From Basic Research to Clinical Therapy
  585. Recombinant Platelet Factor 4: A Therapeutic, Anti-Neoplastic Chimera?
  586. 2009 Eberhard F. Mammen Young Investigator Award Winners
  587. Thrombotic Complications of Erythropoiesis-Stimulating Agents
  588. Shortened activated partial thromboplastin time: causes and management
  589. Quality issues in laboratory haemostasis
  590. Laboratory identification of factor VIII inhibitors in the real world: the experience from Australasia
  591. Laboratory Testing in Disseminated Intravascular Coagulation
  592. Laboratory testing in pharmacies
  593. Improving the harmonisation of the International Normalized Ratio (INR): time to think outside the box?
  594. UNSUSPECTED COAGULOPATHY RARELY PREVENTS IV THROMBOLYSIS IN ACUTE ISCHEMIC STROKE
  595. Laboratory medicine and natural disasters: are we ready for the challenge?
  596. The antiphospholipid syndrome: a large elephant with many parts or an elusive chameleon disguised by many colours?
  597. Problems in laboratory testing: hemophilia and beyond
  598. Under-Recognized Significance of Endothelial Heterogeneity: Hemostasis, Thrombosis, and Beyond
  599. Proteomic analysis of venous thromboembolism
  600. Genetic testing in von Willebrand disease: reply to rebuttal
  601. Prevalence of hypokalaemia: the experience of a large academic hospital
  602. Biochemical markers for the diagnosis of venous thromboembolism: the past, present and future
  603. Platelets, Inflammation and Cardiovascular Diseases. New Concepts and Therapeutic Implications
  604. A laboratory evaluation into the short activated partial thromboplastin time
  605. Mild hemophilia A
  606. Contemporary platelet function testing
  607. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations, Part III
  608. Influenza and Cardiovascular Disease: Does Swine-Origin, 2009 H1N1 Flu Virus Represent a Risk Factor, an Acute Trigger, or Both?
  609. Moderate Red Wine Consumption and Cardiovascular Disease Risk: Beyond the “French Paradox”
  610. Right or wrong sample received for coagulation testing? Tentative algorithms for detection of an incorrect type of sample
  611. Quality in coagulation and haemostasis testing
  612. Hemophilia, cancer and cardiovascular disease
  613. Glanzmann thrombasthenia: An update
  614. Genetic testing for von Willebrand disease: the case against
  615. Evaluation of commercial von Willebrand factor collagen binding assays to assist the discrimination of types 1 and 2 von Willebrand disease
  616. Laboratory reporting of hemostasis assays: the final post-analytical opportunity to reduce errors of clinical diagnosis in hemostasis?
  617. Identification and prevalence of von Willebrand disease type 2N (Normandy) in Australia
  618. Current clinical and laboratory practice for the investigation of the antiphospholipid syndrome: findings from the 2008 Australasian antiphospholipid antibody survey
  619. Emanuele Favaloro (1920–2009) and Francesca Favaloro (1922–2009)
  620. Farewell to 2009!
  621. Identification, Pathogenesis, and Treatment of Factor Inhibitors
  622. Investigations from External Quality Assurance Programs Reveal a High Degree of Variation in the Laboratory Identification of Coagulation Factor Inhibitors
  623. Winners of the Inaugural Eberhard F. Mammen Award for Most Popular Article
  624. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations, Part II
  625. Laboratory Investigation of Thrombophilia: The Good, the Bad, and the Ugly
  626. Unsuspected Triggers of Venous Thromboembolism—Trivial or Not So Trivial?
  627. Prostate-Specific Antigen, Prostate Cancer, and Disorders of Hemostasis
  628. The Bidirectional Relationship of Cancer and Hemostasis and the Potential Role of Anticoagulant Therapy in Moderating Thrombosis and Cancer Spread
  629. Potential supplementary utility of combined PFA-100 and functional von Willebrand factor testing for the laboratory assessment of desmopressin and factor concentrate therapy in von Willebrand disease
  630. Tirofiban and Activated Protein C Synergistically Inhibit the Instant Blood Mediated Inflammatory Reaction (IBMIR) from Allogeneic Islet Cells Exposure to Human Blood
  631. D-Dimer Measurement and Laboratory Feedback
  632. Laboratory assessment and perioperative management of patients on antiplatelet therapy: From the bench to the bedside
  633. Relationship between 24-h air pollution, emergency department admission and diagnosis of acute coronary syndrome
  634. Methodology and outcomes of platelet aggregation testing in Australia, New Zealand and the Asia‐Pacific region: results of a survey from the Royal College of Pathologists of Australasia Haematology Quality Assurance Program
  635. The role of ethnicity, age and gender in venous thromboembolism
  636. Time to seek further clarity in the molecular analysis of von Willebrand disease?
  637. Rare Bleeding Disorders
  638. Rodger L. Bick, M.D., Ph.D., FACP (1943–2008)
  639. Coagulopathies and Thrombosis: Usual and Unusual Causes and Associations, Part I
  640. Mental Depression and Cardiovascular Disease: A Multifaceted, Bidirectional Association
  641. Desmopressin therapy to assist the functional identification and characterisation of von Willebrand disease: Differential utility from combining two (VWF:CB and VWF:RCo) von Willebrand factor activity assays?
  642. Internal Quality Control and External Quality Assurance of Platelet Function Tests
  643. Diagnostic Evaluation of Platelet Disorders: The Past, the Present, and the Future
  644. Welcome to the First Issue of Seminars in Thrombosis and Hemostasis for 2009
  645. Milestones and Perspectives in Coagulation and Hemostasis
  646. Relationship between activated partial thromboplastin time, heparin and potassium levels
  647. Laboratory Diagnostics and Therapy in Thrombosis and Hemostasis: From Bedside to Bench to Bedside
  648. Toward a New Paradigm for the Identification and Functional Characterization of von Willebrand Disease
  649. High Rate of Deficiency in the Amino Acids Tryptophan and Histidine in People with Wounds
  650. The missing link between genotype, phenotype and clinics
  651. Pharmacogenetics of vitamin K antagonists: useful or hype?
  652. The Journal Impact Factor: don't expect its demise any time soon
  653. Diagnosis of von willebrand disease (VWD): towards a new paradigm for the identification and functional characterisation of VWD
  654. One-stage clotting versus chromogenic assays for assessing recombinant factor VIII: two faces of a haemostasis coin
  655. Survey on the prevalence of hemolytic specimens in an academic hospital according to collection facility: opportunities for quality improvement
  656. Epidemiological association between fasting plasma glucose and shortened APTT
  657. Laboratory Evaluation of von Willebrand Disease: Phenotypic Analysis
  658. Aspirin ‘responsiveness’, ‘nonresponsiveness’ or ‘resistance’: a putative role for von Willebrand factor?
  659. Welcome to a Special Issue of Seminars in Thrombosis and Hemostasis —The Closing Issue for 2008
  660. A Tribute to Eberhard F. Mammen, M.D. (1930–2008)
  661. Clinical Utility of the PFA-100
  662. Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD): a rebuttal
  663. Activated Partial Thromboplastin Time: New Tricks for an Old Dogma
  664. Laboratory Diagnostics in Thrombosis and Hemostasis: The Past, the Present, and the Future
  665. Standardization of the INR: How Good Is Your Laboratory's INR and Can It Be Improved?
  666. Preanalytical and Postanalytical Variables: The Leading Causes of Diagnostic Error in Hemostasis?
  667. Dark chocolate: consumption for pleasure or therapy?
  668. Hyperthyroidism is associated with shortened APTT and increased fibrinogen values in a general population of unselected outpatients
  669. Salbutamol in Athletes
  670. Genetics of type 2B von Willebrand Disease: “True 2B,” “tricky 2B,” or “Not 2B.” What Are the Modifiers of the Phenotype?
  671. A better approach to monitoring of therapy in von Willebrand disease?
  672. Updates on improvement of human athletic performance: focus on world records in athletics
  673. Differential identification of PT‐VWD from type 2B VWD and GP1BA nomenclature issues response to Othman
  674. The genetic basis of human athletic performance. Why are psychological components so often overlooked?
  675. Antiphospholipid Antibodies and the Antiphospholipid Syndrome II: Limitations, Standardization, and Clinical Utility of Laboratory Testing
  676. Laboratory Testing and Identification of Antiphospholipid Antibodies and the Antiphospholipid Syndrome: A Potpourri of Problems, a Compilation of Possible Solutions
  677. A Consensus Approach to the Formulation of Guidelines for Laboratory Testing and Reporting of Antiphospholipid Antibody Assays
  678. The paradoxical relationship between serum uric acid and cardiovascular disease
  679. Cardiac biomarkers in pulmonary embolism
  680. Stability of coagulation assays performed in plasma from citrated whole blood transported at ambient temperature: Only a part of the story
  681. Potential benefits of improved protein intake in older people
  682. Clinical Features, Diagnosis, and Management of the Antiphospholipid Syndrome
  683. Professor Ronald A. Asherson, M.D. (Hon), F.R.C.P., M.D., F.A.C.P., F.C.P., F.A.C.R., Dip. O&G (Hon) [1934–2008]
  684. Antiphospholipid Antibodies and the Antiphospholipid Syndrome I: Pathogenesis, Clinical Features, Diagnosis, and Management
  685. The LOC387715 Polymorphism, Inflammatory Markers, Smoking, and Age-Related Macular Degeneration
  686. Time to think outside the box? Prothrombin time, international normalised ratio, international sensitivity index, mean normal prothrombin time and measurement of uncertainty a novel approach to standardisation
  687. Can blood flow assays help to identify clinically relevant differences in von Willebrand factor functionality in von Willebrand disease types 1–3?
  688. von Willebrand disease, type 2B: A diagnosis more elusive than previously thought
  689. Welcome to Seminars in Thrombosis and Hemostasis -2008!
  690. Measuring the Quality of Journals and Journal Articles: The Impact Factor Tells but a Portion of the Story
  691. Hot Topics II: An Editorial Collection of Current Issues and Controversies in Thrombosis and Hemostasis
  692. Phenotypic Identification of Platelet-Type von Willebrand Disease and Its Discrimination from Type 2B von Willebrand Disease: A Question of 2B or Not 2B? A Story of Nonidentical Twins? Or Two Sides of a Multidenominational or Multifaceted Primary-Hemos...
  693. Detection of duplicates and redundancies. A major responsibility of peer-reviewers?
  694. Help me, Doctor! My D-dimer is raised
  695. Protein Z is reduced in chronic kidney disease and not elevated in patients on haemodialysis
  696. Air pollution and coagulation testing: A new source of biological variability?
  697. A practical approach to instrument selection, evaluation, basic financial management and implementation in pathology and research
  698. Consensus guidelines on anti-beta 2 glycoprotein I testing and reporting
  699. The Diagnostic Dilemma: Dual Presentations of Clinical Mucosal Bleeding and Venous Thrombosis Associated with the Presence of Thrombophilia Markers and Mild Reduction in von Willebrand Factor
  700. Hot Topics I: A Potpourri of Current Issues and Controversies in Thrombosis and Hemostasis
  701. An Update on the von Willebrand Factor Collagen Binding Assay: 21 Years of Age and Beyond Adolescence but Not Yet a Mature Adult
  702. Hemostatic Dysfunction Associated with Endocrine Disorders as a Major Risk Factor and Cause of Human Morbidity and Mortality: A Comprehensive Meta-review
  703. Time to Think Outside the Box? Proposals for a New Approach to Future Pharmacokinetic Studies of von Willebrand Factor Concentrates in People with von Willebrand Disease
  704. Differential identification of a rare form of platelet‐type (pseudo‐) von Willebrand disease (VWD) from Type 2B VWD using a simplified ristocetin‐induced‐platelet‐agglutination mixing assay and confirmed by genetic analysis
  705. Mis-identification of factor inhibitors by diagnostic haemostasis laboratories: recognition of pitfalls and elucidation of strategies. A follow up to a large multicentre evaluation
  706. More on the impact factor and thrombosis and haemostasis journals: Benefits and limitations
  707. 2B or not 2B? Disparate discrimination of functional VWF discordance using different assay panels or methodologies may lead to success or failure in the early identification of type 2B VWD
  708. Utility of the PFA-100 as a screening test of platelet function: an audit of haemostasis laboratories in Australia and New Zealand
  709. Circulating Inflammatory Markers and Hemostatic Factors in Age-Related Maculopathy: A Population-Based Case–Control Study
  710. Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder. A randomised cross-over, multi-centre study
  711. Standardization, Quality Assurance, and Emerging Diagnostic Technologies in Hemostasis
  712. Emerging Technologies and Quality Assurance in Hemostasis: A Review of Findings from the Royal College of Pathologists of Australasia Quality Assurance Program
  713. Standardization, Regulation, Quality Assurance and Emerging Technologies in Hemostasis: Issues, Controversies, Benefits, and Limitations
  714. A Review of β 2 -Glycoprotein-I Antibody Testing Results From a Peer-Driven Multilaboratory Quality Assurance Program
  715. Investigating people with mucocutaneous bleeding suggestive of primary hemostatic defects: a low likelihood of a definitive diagnosis?
  716. Erratum
  717. Preanalytical variables in coagulation testing
  718. Thrombophilia and Cerebral Vein Thrombosis
  719. Increased Propensity to Bruising in Red-Haired Females: A Possible Role for von Willebrand Factor?
  720. 2B or not 2B? Differential identification of type 2B, versus pseudo‐, von Willebrand disease – response to Whalley and Perry
  721. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
  722. Laboratory Monitoring of Therapy in von Willebrand Disease: Efficacy of the PFA-100 and von Willebrand Factor:Collagen-Binding Activity as Coupled Strategies
  723. More on: platelet function analyser (PFA)‐100® closure time in the evaluation of platelet disorders and platelet function
  724. Acquired von Willebrand disease: potential contribution of the VWF:CB to the identification of functionally inhibiting auto‐antibodies to von Willebrand factor
  725. 2B or not 2B? Differential identification of type 2B, versus pseudo‐von Willebrand disease
  726. Laboratory Identification of von Willebrand Disease: Technical and Scientific Perspectives
  727. The Utility of the PFA-100 in the Identification of von Willebrand Disease: A Concise Review
  728. Reducing Errors in Identification of von Willebrand Disease: The Experience of the Royal College of Pathologists of Australasia Quality Assurance Program
  729. More on ‘universal’versus‘selected’ screening for thrombophilia: the hidden costs of false‐positive diagnosis
  730. Identification of factor inhibitors by diagnostic haemostasis laboratories. A large multi-centre evaluation
  731. Unrecognized pellagra masquerading as odynophagia
  732. Abstracts from the 24th Annual Scientific Meeting
  733. The reactivity of paired plasma and serum samples are comparable in the anticardiolipin and anti‐β2‐glycoprotein‐1 ELISAs: a rebuttal
  734. Effect of overnight 4°C storage of whole blood on von Willebrand factor
  735. 2B or not 2B? What is the role of VWF in platelet–matrix interactions? And what is the role of the VWF:CB in VWD diagnostics? These are the questions
  736. Activated protein C resistance: The influence of ABO-blood group, gender and age
  737. Cold storage of citrated whole blood induces drastic time-dependent losses in factor VIII and von Willebrand factor: potential for misdiagnosis of haemophilia and von Willebrand disease
  738. Reassessment of ABO Blood Group, Sex, and Age on Laboratory Parameters Used to Diagnose von Willebrand Disorder
  739. Reassessment of ABO Blood Group, Sex, and Age on Laboratory Parameters Used to Diagnose von Willebrand Disorder
  740. Cross-laboratory audit of normal reference ranges and assessment of ABO blood group, gender and age on detected levels of plasma coagulation factors
  741. How Useful is the Monitoring of (Low Molecular Weight) Heparin Therapy by Anti-Xa Assay? A Laboratory Perspective
  742. Laboratory Identification of Familial Thrombophilia: Do the Pitfalls Exceed the Benefits? A Reassessment of ABO-Blood Group, Gender,Age, and other Laboratory Parameters on the Potential Influence on a Diagnosis of Protein C, Protein S, and Antithromb
  743. A Diet Rich in High-Oleic-Acid Sunflower Oil Favorably Alters Low-Density Lipoprotein Cholesterol, Triglycerides, and Factor VII Coagulant Activity
  744. An international survey of current practice in the laboratory assessment of anticoagulant therapy with heparin
  745. Laboratory Diagnosis of von Willebrand Disorder: Use of Multiple Functional Assays Reduces Diagnostic Error Rates
  746. Diagnostic Issues in Thrombophilia: A Laboratory Scientist's View
  747. External Quality Assurance of DNA Testing for Thrombophilia Mutations
  748. Development of Consensus Guidelines for Anticardiolipin and Lupus Anticoagulant Testing
  749. Learning from Peer Assessment: The Role of the External Quality Assurance Multilaboratory Thrombophilia Test Process
  750. Multilaboratory Testing of Thrombophilia: Current and Past Practice in Australasia as Assessed through the Royal College of Pathologists of Australasia Quality Assurance Program for Hematology
  751. A Multilaboratory Peer Assessment Quality Assurance Program-Based Evaluation of Anticardiolipin Antibody, and beta 2 -Glycoprotein I Antibody Testing
  752. Is elevated factor VIII a risk factor for venous thromboembolism in Canada?
  753. Factor V inhibitors
  754. Template bleeding time and PFA‐100® have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: comparative study of 148 patients – a rebuttal
  755. Potential Laboratory Misdiagnosis of Hemophilia and von Willebrand Disorder Owing to Cold Activation of Blood Samples for Testing
  756. Potential Laboratory Misdiagnosis of Hemophilia and von Willebrand Disorder Owing to Cold Activation of Blood Samples for Testing
  757. Evaluation of primary haemostasis in people with neurofibromatosis type 1
  758. von Willebrand disease: laboratory aspects of diagnosis and treatment
  759. Laboratory diagnosis of von Willebrand's disorder: quality and diagnostic improvements driven by peer review in a multilaboratory test process
  760. A multi-centre evaluation of the intra-assay and inter-assay variation of commercial and in-house anti-cardiolipin antibody assays
  761. Consensus guidelines on anti-cardiolipin antibody testing and reporting
  762. Laboratory Diagnosis of von Willebrand Disorder
  763. Laboratory Diagnosis of von Willebrand Disorder: Current Practice in the Southern Hemisphere
  764. A duplex issue: (i) time to re‐appraise the diagnosis and classification of von Willebrand disorder, and (ii) clarification of the roles of von Willebrand factor collagen binding and ristocetin cofactor activity assays
  765. Assessing the Usefulness of Anticardiolipin Antibody Assays
  766. Clinical application of the PFA-100®
  767. Identification of von Willebrand Disease Type 2N (Normandy) in Australia
  768. Treatment of two patients with acquired factor VIII inhibitors using cyclophosphamide and prednisone
  769. von Willebrand Factor Collagen-Binding (Activity) Assay in the Diagnosis of von Willebrand Disease: A 15-Year Journey
  770. A 9-year retrospective assessment of laboratory testing for activated protein C resistance: evolution of a novel approach to thrombophilia investigations
  771. Nitric Oxide and Prostacyclin are Released by Cultured Apoptotic Human Umbilical Vein Endothelial Cells Consistent with an Anti-Micro-Thrombotic Potential
  772. A Comparative Multi-laboratory Assessment of Three Factor VIII/von Willebrand Factor Concentrates
  773. Appropriate laboratory assessment as a critical facet in the proper diagnosis and classification of von Willebrand disorder
  774. Utility of the PFA‐100® for assessing bleeding disorders and monitoring therapy: a review of analytical variables, benefits and limitations
  775. Laboratory diagnosis of von Willebrand disorder (vWD) and monitoring of DDAVP therapy: efficacy of the PFA‐100® and vWF:CBA as combined diagnostic strategies
  776. Possibility of potential VWD misdiagnosis or misclassification using LIA technology and due to presence of rheumatoid factor
  777. Collection and Transport of Samples for Laboratory Testing in von Willebrand’s Disease (VWD): Time for a Reappraisal?
  778. Human Endothelial Cells Maintain Anti-Aggregatory Activity for Platelets during Apoptosis
  779. Assessment of current diagnostic practice and efficacy in testing for von Willebrand's disorder: results from the second Australasian multi-laboratory survey
  780. Detection of von Willebrand Disorder and Identification of Qualitative von Willebrand Factor Defects Direct Comparison of Commercial ELISA-Based von Willebrand Factor Activity Options
  781. Is the activity of VWF increased in type II diabetes mellitus?
  782. Sulfatide-Binding Assay for von Willebrand Factor
  783. Type 2B von Willebrand's disease in thirteen individuals from five unrelated Australian families: Phenotype and genotype correlations
  784. Possibility of potential VWD misdiagnosis or misclassification using LIA technology and due to presence of rheumatoid factor
  785. Discrimination of von Willebrands Disease (VWD) Subtypes: Direct Comparison of von Willebrand Factor:Collagen Binding Assay (VWF:CBA) with Monoclonal Antibody (MAB) Based VWF-capture Systems
  786. Structure and function of the von Willebrand factor A1 domain: analysis with monoclonal antibodies reveals distinct binding sites involved in recognition of the platelet membrane glycoprotein Ib-IX-V complex and ristocetin-dependent activation
  787. Collagen Binding Assay for von Willebrand Factor (VWF:CBA): Detection of von Willebrands Disease (VWD), and Discrimination of VWD Subtypes, Depends on Collagen Source
  788. Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand’s disease
  789. Use of a novel platelet function analyzer (PFA‐100™) with high sensitivity to disturbances in von willebrand factor to screen for von willebrand's disease and other disorders
  790. Use of a novel platelet function analyzer (PFA-100?) with high sensitivity to disturbances in von willebrand factor to screen for von willebrand's disease and other disorders
  791. Mesenteric vein thrombosis secondary to combined protein C deficiency and double heterozygosity for factor V leiden and prothrombin G20210A
  792. Mesenteric vein thrombosis secondary to combined protein C deficiency and double heterozygosity for factor V leiden and prothrombin G20210A
  793. Laboratory Testing, Diagnosis, and Management of von Willebrand Disease: Current Practice in Australasia
  794. Identification and characterization of a novel mutation in von Willebrand factor causing type 2B von Willebrand's disease
  795. Clinical utility of anticardiolipin antibody assays: high inter-laboratory variation and limited consensus by participants of external quality assurance programs signals a cautious approach
  796. Comparison of the effects of two low fat diets with different α-linolenic:linoleic acid ratios on coagulation and fibrinolysis
  797. A Novel Factor V Null Mutation at Arg 506 Causes a False Positive Factor V Leiden Result
  798. Laboratory Testing for von Willebrand’s Disease: An Assessment of Current Diagnostic Practice and Efficacy by Means of a Multi-laboratory Survey
  799. Type 2B von Willebrand’s Disease and Angiodysplasia
  800. Medical research in New South Wales 1993–1996 assessed by Medline publication capture
  801. A Simple, Whole Blood Method for Assessment of Platelet Function
  802. Biliary fibronectin: Significant limitation as a diagnostic tool in malignant biliary obstruction
  803. Laboratory Assessment of von Willebrand Factor: Altered Interpretation of Laboratory Data, and Altered Diagnosis of von Willebrand's Disease
  804. The MDA-180 coagulation analyser: a laboratory evaluation
  805. Laboratory assays for von Willebrand Factor: relative contribution to the diagnosis of von Willebrand’s disease
  806. Laboratory assessment of von Willebrand factor: differential influence of prolonged ambient temperature specimen storage on assay results
  807. Cardiovascular Risk Factors and Dietary Plant Omega-3 Verus Omega-6 Fatty Acids
  808. MUTATIONS IN A SUBGROUP OF PATIENTS WITH MILD HAEMOPHILIA A AND A FAMILIAL DISCREPANCY BETWEEN THE ONE‐STAGE AND TWO‐STAGE FACTOR VIII:C METHODS
  809. A survey of heparin monitoring in australasia
  810. Aminopeptidase-N (CD13; gp 150): Contrasting patterns of enzymatic activity in blood from patients with myeloid or lymphoid leukemia
  811. Laboratory Assessment of von Willebrand Factor:Use of Different Assays Can Influence the Diagnosis of von Willebrand’s Disease, Dependent on Differing Sensitivity to Sample Preparation and Differential Recognition of High Molecular Weight VWF Forms
  812. Attenuated platelet sensitivity to collagen in patients with neurofibromatosis type 1
  813. von Willebrand's disease: Use of collagen binding assay provides potential improvement to laboratory monitoring of desmopressin (DDAVP) therapy
  814. Differential expression of surface antigens on activated endothelium
  815. The hepatobiliary disease marker serum alanine aminopeptidase predominantly comprises an isoform of the haematological myeloid differentiation antigen and leukaemia marker CD-13/gp150
  816. Acidified Chloroquine Treatment for the Removal of Class I HLA Antigens
  817. Von willebrand's disease: laboratory investigation using an improved functional assay for von willebrand factor
  818. Characterization of GMP-140 (P-selectin) as a circulating plasma protein.
  819. Heparin - induced thrombocytopenia: laboratory investigation and confirmation of diagnosis
  820. CD‐13 (‘gp150’; aminopeptidase‐N): Co‐expression on endothelial and haemopoietic cells with conservation of functional activity
  821. Development of a simple collagen based ELISA assay aids in the diagnosis of, and permits sensitive discrimination between Type I and Type II, von Willebrand??s disease
  822. Co‐expression of haemopoietic antigens on vascular endothelial cells: a detailed phenotypic analysis
  823. Endothelial Cells and Normal Circulating Haemopoietic Cells Share a Number of Surface Antigens
  824. Further characterization of human myeloid antigens (gp160,95; gp150; gp67): investigation of epitopic heterogeneity and non‐haemopoietic distribution using panels of monoclonal antibodies belonging to CD‐11b, CD‐13 and CD‐33
  825. Immunophenotype of clonogenic cells in myeloid leukaemia
  826. Further studies on the heterogeneity of antigens recognised by CD‐1 monoclonal antibodies: distribution of epitopes and analysis of serological binding patterns
  827. Further studies on the heterogeneity of antigens recognised by CD‐1 monoclonal antibodies: distribution of epitopes and analysis of serological binding patterns
  828. TRANSPLANTATION OF MONOCLONAL ANTIBODY‐PURGED AUTOLOGOUS BONE MARROW FOR TREATMENT OF POOR RISK COMMON ACUTE LYMPHOBLASTIC LEUKEMIA
  829. Coexpression of p165 myeloid surface antigen and terminal deoxynucleotidyl transferase: A comparison of acute myeloid leukaemia and normal bone marrow cells
  830. Standardization of monoclonal antibodies for use in autologous bone marrow transplantation for common acute lymphoblastic leukemia
  831. Myeloid progenitor surface antigen identified by monoclonal antibody
  832. Human myeloid differentiation antigens identified by monoclonal antibodies: expression on leukemic cells
  833. The role of buffer anions and protons in secretion by the rabbit mandibular salivary gland.