Latest Research in Platelet Disorders and Treatments

15 research papers · 2026 median publication year

Top Research Topics in Platelet Disorders and Treatments

Highest-Cited Papers

  1. Analysis of Annual Global Survey Reports for Haemophilia B in the Eastern Mediterranean Region: Disparities in Trends for A decade (2014–2023)
  2. DDAVP Challenges in 170 Children With von Willebrand Disease: Response Classification Varies According to Criteria Used
  3. Congenital Hemophilia‐A With High‐Titer Inhibitor and Essential Thrombocythemia: A Rare Coexistence
  4. From Biological Insight to a New Class of Medicines for Hemophilia A
  5. Deficiency of high‐molecular‐weight von Willebrand factor mitigates thrombo‐complement injury in an LPS‐induced TMA‐like mouse model
  6. Factor VIII inhibitors demonstrate type I or type II kinetics in high‐titre alloantibodies and autoantibodies
  7. Akhirin Preserves Hemostatic Wound Repair Through Non-Hematopoietic Regulation of the Vascular Injury Microenvironment
  8. Utilizing Inhibitor Screening Assay Results to Predict Bethesda Titers in Patients With Hemophilia A: Cost‐Effective Strategy in Resource‐Constrained Setting
  9. Use of C1 Inhibitor Subcutaneously in the United Kingdom: Insights from a National Real-World Retrospective Study
  10. Acquired hemophilia: insights from a multicenter real-life study in a middle-income country
  11. Single versus double lung transplantation in patients with pneumoconiosis: a retrospective cohort study
  12. Prediction of coagulation factor inhibitor levels using Random Forest model based on the activated partial thromboplastin time (aPTT) mixing study: model development and prototype application
  13. Population‐Level Real‐World Healthcare Costs in Men and Women With Haemophilia A
  14. Whole genome sequencing to elucidate novel genetic modifiers of FVIII clearance.
  15. Persistent Hypersensitivity Reactions Associated With Anti‐PEG IgM Antibodies During On‐Demand Therapy With PEGylated Factor VIII in Mild Hemophilia A
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L3 Region - - 2026 Sep Q3

Platelet Disorders and Treatments

15 papers

Top Topics (6)

Hemophilia Treatment and Research10
Platelet Disorders and Treatments1
Complement system in diseases1
Barrier Structure and Function Studies1
Coagulation, Bradykinin, Polyphosphates, and Angioedema1
Transplantation: Methods and Outcomes1

Top Publications (15)

1.Analysis of Annual Global Survey Reports for Haemophilia B in the Eastern Mediterranean Region: Disparities in Trends for A decade (2014–2023)2.DDAVP Challenges in 170 Children With von Willebrand Disease: Response Classification Varies According to Criteria Used3.Congenital Hemophilia‐A With High‐Titer Inhibitor and Essential Thrombocythemia: A Rare Coexistence4.From Biological Insight to a New Class of Medicines for Hemophilia A5.Deficiency of high‐molecular‐weight von Willebrand factor mitigates thrombo‐complement injury in an LPS‐induced TMA‐like mouse model6.Factor VIII inhibitors demonstrate type I or type II kinetics in high‐titre alloantibodies and autoantibodies7.Akhirin Preserves Hemostatic Wound Repair Through Non-Hematopoietic Regulation of the Vascular Injury Microenvironment8.Utilizing Inhibitor Screening Assay Results to Predict Bethesda Titers in Patients With Hemophilia A: Cost‐Effective Strategy in Resource‐Constrained Setting9.Use of C1 Inhibitor Subcutaneously in the United Kingdom: Insights from a National Real-World Retrospective Study10.Acquired hemophilia: insights from a multicenter real-life study in a middle-income country11.Single versus double lung transplantation in patients with pneumoconiosis: a retrospective cohort study12.Prediction of coagulation factor inhibitor levels using Random Forest model based on the activated partial thromboplastin time (aPTT) mixing study: model development and prototype application13.Population‐Level Real‐World Healthcare Costs in Men and Women With Haemophilia A14.Whole genome sequencing to elucidate novel genetic modifiers of FVIII clearance.15.Persistent Hypersensitivity Reactions Associated With Anti‐PEG IgM Antibodies During On‐Demand Therapy With PEGylated Factor VIII in Mild Hemophilia A
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