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Pediatric Blood & Cancer|January 20, 2025
Improving Completion Rates of Transcranial Doppler Ultrasounds in Children With Sickle Cell Disease Using Quality Improvement Efforts: In-Clinic Versus Population-Based AssessmentsMadhav Vissa, Priya Parikh, Chuck McCulloch, et al.Thrombosis and Haemostasis|January 22, 2016
Dok-1 negatively regulates platelet integrin αIIbβ3 outside-in signalling and inhibits thrombosis in miceMasaru Niki, Manasa K Nayak, Hong Jin, et al.Blood Advances|April 26, 2024
DISPLACE study shows poor quality of transcranial doppler ultrasound for stroke risk screening in sickle cell anemiaKimberly A Davidow, Robin E Miller, Shannon M Phillips, et al.Annals of Hematology|April 20, 2024
Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panelJulie Kanter, Kenneth I Ataga, Neha Bhasin, et al.Frontiers in Genetics|September 12, 2022
Barriers to hydroxyurea use from the perspectives of providers, individuals with sickle cell disease, and families: Report from a U.S. regional collaborativeMarsha J Treadwell, Lisa Du, Neha Bhasin, et al.Pediatric Quality & Safety|January 7, 2021
Improving Preventive Care for Children With Sickle Cell Anemia: A Quality Improvement InitiativeMichael D Cabana, Anne Marsh, Marsha J Treadwell, et al.JAMA Network Open|November 13, 2025
National Alliance of Sickle Cell Centers Consensus Recommendations on Sickle Cell Disease Health Maintenance: A Consensus StatementSeethal A Jacob, Melissa Frei-Jones, Sana Saif-Ur-Rehman, et al.Implementation Science : IS|November 27, 2025
Successful implementation of stroke risk screening for sickle cell anemia in the DISPLACE study: results of a cluster randomized trialAlyssa M Schlenz, Shannon M Phillips, Martina Mueller, et al.JAMA Network Open|December 9, 2025
Role of Menstrual Bleeding Assessments in Sickle Cell ClinicsGillian Rush, Rania E Mohamed, Kimberly Moffatt-Bazile, et al.Pediatric Blood & Cancer|March 7, 2025
Engaging Parents of Children With Sickle Cell Disease in Shared Decision-Making for Hydroxyurea: The ENGAGE-HU StudyAimee K Hildenbrand, Constance A Mara, Bridget Murphy, et al.Pageof 2