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3. Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial)

4. A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

5. The Grndad Registry: Contemporary Natural History Data and an Analysis of Real-World Patterns of Use and Limitations of Disease Modifying Therapy in Adults with SCD

6. Sickle Cell Disease

7. Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial

8. Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial (Preprint)

9. A Phase 3 Trial of<scp>l</scp>-Glutamine in Sickle Cell Disease

10. Encephaloduroarteriosynangiosis (EDAS) in young patients with cerebrovascular complications of sickle cell disease: Single-institution experience

11. Addressing Recruitment Challenges in the Engage-HU Trial in Young Children with Sickle Cell Disease

12. Osteonecrosis in sickle cell disease: an update on risk factors, diagnosis, and management

13. Sickle Cell Disease: Monitoring, Current Treatment, and Therapeutics Under Development

14. Safety and efficacy of deferiprone for pantothenate kinase-associated neurodegeneration: a randomised, double-blind, controlled trial and an open-label extension study

15. Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and stroke

16. Stroke recurrence in adult sickle cell patients: it is time for action!

17. Differential Acetone Extraction of Total and Hemoprotein-Unbound Heme to Quantify Heme Binding Capacity of Plasma in Patients with Sickle Cell Disease: The Role of Heme Scavengers

18. Population based surveillance in sickle cell disease: Methods, findings and implications from the California registry and surveillance system in hemoglobinopathies project (RuSH)

19. Clinical Practice Patterns for Hydroxyurea Initiation in Young Children with Sickle Cell Disease

20. Chronic Kidney Disease Is Under-Screened in SCD and Mild Albuminuria Is Associated with a Drop in Hemoglobin: A Report from the Grndad Sickle Cell Registry

21. Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

22. A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

23. Combined chelation therapy with deferasirox and deferoxamine in thalassemia

25. Erythrocytapheresis for chronic transfusion therapy in sickle cell disease: survey of current practices and review of the literature

26. A phase 1/2 trial of HQK-1001, an oral fetal globin inducer, in sickle cell disease

27. The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial

28. Abstract T P369: Increased Prevalence of Potential Right-to-Left Shunting in Children with Sickle Cell Anemia and Stroke

29. Physical Therapy Alone Compared with Core Decompression and Physical Therapy for Femoral Head Osteonecrosis in Sickle Cell Disease

30. Systemic Biomarkers Show Elevated Oxidative Stress and Chronic Inflammation in Two Disorders of Neurodegeneration with Brain Iron Accumulation (NBIA)

31. Red blood cell transfusion in pediatric patients with severe chronic anemia: How slow is necessary?

32. Mechanisms of plasma non-transferrin bound iron generation: insights from comparing transfused diamond blackfan anaemia with sickle cell and thalassaemia patients

33. Population based surveillance in sickle cell disease: methods, findings and implications from the California registry and surveillance system in hemoglobinopathies project (RuSH)

34. Neuroimaging abnormalities in adults with sickle cell anemia: associations with cognition

35. Severity of iron overload in patients with sickle cell disease receiving chronic red blood cell transfusion therapy

36. The perioperative complication rate of orthopedic surgery in sickle cell disease: Report of the national sickle cell surgery study group

37. Tonsillectomy, Adenoidectomy, and Myringotomy in Sickle Cell Disease

38. Surgery in patients with hemoglobin SC disease

39. Emergency department utilization by Californians with sickle cell disease, 2005-2014

41. A Comparison of Conservative and Aggressive Transfusion Regimens in the Perioperative Management of Sickle Cell Disease

42. Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

43. Improved engraftment with minimal graft-versus-host disease after major histocompatibility complex-mismatched cord blood transplantation with photochemically treated donor lymphocytes

44. The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial

45. Fracture Prevalence and Relationship to Endocrinopathy in Iron Overloaded Patients with Sickle Cell Disease and Thalassemia

46. Iron Level and Monocyte Morphology Predict TLR4 Expression and Reactive Oxygen Species Production Which Influences Chronic Inflammation in β-Thalassemia

47. Bone and joint disease in sickle cell disease

48. Clinical evaluation of avascular necrosis in patients with sickle cell disease: Children's Hospital Oakland Hip Evaluation Scale--a modification of the Harris Hip Score

49. Mycoplasma disease and acute chest syndrome in sickle cell disease

50. Chlamydia pneumoniae and acute chest syndrome in patients with sickle cell disease

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