36 results on '"Ward, Richard"'
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2. "It's Kind of a Hidden Code": An Exploratory Study of Residents’ Experiences Caring for People with Sickle Cell Disease on the Internal Medicine Wards
3. The antiparasitic agent ivermectin induces chloride-dependent membrane hyperpolarization and cell death in leukemia cells
4. The Monocyte Monolayer Assay to Build a Personalized Pipeline of Transfusion Support in Highly Sensitized Sickle Cell Disease
5. Risk Factors for Postnatal Complications in People with Sickle Cell Disease: A Preliminary Analysis
6. Predictors of the Rowland Universal Dementia Assessment Scale (RUDAS) Performance in Adults with Sickle Cell Disease
7. Patient Education Interventions for Improving Self-Management in Adults with Hemoglobinopathies: A Systematic Review and Meta-Analysis
8. Prediction of Risk for Adverse Pregnancy Outcomes in Women with Sickle Cell Disease
9. Rate of Sickle Hemoglobin Recovery in Sickle Cell Disease Patients Undergoing Red Blood Cell (RBC) Exchange Transfusion Is Associated with Age of Patients and Number of RBC Units Transfused
10. Should Women with Sickle Cell Disease be Administered Prophylactic Transfusions to Avoid Complications during Pregnancy?
11. Is There a Role for Thromboprophylaxis in Sickle Cell Patients with Central Venous Access Devices?
12. Examining the Role of Sickle Cell Disease Patients As Teachers in the Emergency Department: Patient Directed Physician Education
13. Real World Experience with Sublingual Fentanyl for the Treatment of Sickle Cell Vaso-Occlusive Episodes in Adults in a Tertiary Canadian Emergency Department
14. Validation of Sickle Cell Disease Severity Score in a Cohort of Hemoglobin SC Disease Patients
15. Pilot Study of Online Learning Modules for Hemoglobinopathy Education in Canadian Hematology Training Programs
16. Factors Impacting Quality of Life in Thalassemia Patients; Results from the Intercontinenthal Collaborative Study
17. Comprehensive Structured Transition Program with Dedicated Transition Navigator Reduced Lost to Follow-up and Improved Medication Adherence in Sickle Cell Disease and Thalassemia Adolescents and Young Adults
18. An Unusual Case of Acquired Hemophilia a and Factor XIII Consumption
19. Hemoglobinopathy Education in Canadian Hematology Training Programs: How Much Are Residents Learning?
20. Treatment Patterns and Outcomes Of Sickle Cell Patients With Frequent ER Visits: A Single Center Experience
21. A North American Experience Of Hemoglobin SC Disease, Its Complications, and Management
22. Effectiveness Of An Analgesia Protocol For The Treatment Of Painful Vaso-Occlusive Crisis Of Sickle Cell Disease Patients In Emergency Room: A Retrospective Cohort Study
23. Characterization Of Pulmonary Compliance In Sickle Cell Patients Revealed Wide Variability
24. A Comparison of Chronic Manual and Automated Red Blood Cell Exchange Transfusion in Sickle Cell Disease Patients From Two Comprehensive Care Centres in the United Kingdom
25. A Randomized, Open-Label, Multicenter, Dose Escalation Study of HQK-1001 (2,2-Dimethylbutyrate, Sodium Salt) in Sickle Cell Disease
26. Comparing Patterns for Transitioning the Care of Young Adults with Sickle Cell Disease Versus Hemophilia: The Toronto Experience
27. Effectiveness, Time Utilization and Clinical Outcome of Partial Manual Red Cell Exchange in Patients with Sickle Cell Disease
28. Single-Centre, North American Experience with Compassionate Use of Deferiprone in Patients with Beta-Thalassemia Major,
29. Application of Self-Efficacy Theory in Adherence to Iron Chelation Therapy: A Single-Center Cross-Sectional Study
30. Heterogeneity In Regional Myocardial T2* Improvement After Deferiprone Therapy,
31. The Effect of Comprehensive Care on Maternal and Fetal Outcomes in Sickle Cell Disease Pregnancies
32. The Effect of Comprehensive Care and Degree of Iron Overload on Maternal and Fetal Outcomes in Pregnancies of Transfusion-Dependent Beta-Thalassemia Patients
33. Feasibility of Outpatient Consolidation Chemotherapy and Toxicity in Elderly Patients with AML.
34. A Prospective Study of Voriconazole Therapeutic Drug Monitoring (TDM) in Patients with Acute Leukemia.
35. Low-Level FLT3-ITD Mutations Do Not Predict for Higher Relapse Rate in AML with Standard Risk Karyotpye.
36. Prophylactic transfusion for pregnant women with sickle cell disease: a systematic review and meta-analysis.
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