All Stories

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