1,012 results on '"Ballas, Samir K"'
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2. Opioids are not a major cause of death of patients with sickle cell disease
3. Review/overview of pain in sickle cell disease
4. Risk factors associated with increased emergency department utilization in patients with sickle cell disease: a systematic literature review
5. Opioid Utilization by Pregnant Women with Sickle Cell Disease and the Risk of Neonatal Abstinence Syndrome
6. Systematic review and meta-analysis of the effect of iron chelation therapy on overall survival and disease progression in patients with lower-risk myelodysplastic syndromes
7. The role of blood rheology in sickle cell disease
8. Sickle cell disease chronic joint pain: Clinical assessment based on maladaptive central nervous system plasticity
9. Plasmapheresis may improve clinical condition in sickle cell disease through its effects on red blood cell rheology
10. Red blood cell exchange: 2015 American Society for Apheresis consensus conference on the management of patients with sickle cell disease
11. From total blood exchange to erythrocytapheresis and back to treat complications of sickle cell disease
12. Sickle cell pain: a critical reappraisal
13. Sickle Cell Disease Chronic Joint Pain: Clinical Assessment Based on Maladaptive Central Nervous System Plasticity
14. High mortality among children with sickle cell anemia and overt stroke who discontinue blood transfusion after transition to an adult program
15. Safety and efficacy of blood exchange transfusion for priapism complicating sickle cell disease
16. The Impact of Hydroxyurea on Career and Employment of Patients With Sickle Cell Anemia
17. Hydroxyurea and Acute Painful Crises in Sickle Cell Anemia: Effects on Hospital Length of Stay and Opioid Utilization During Hospitalization, Outpatient Acute Care Contacts, and at Home
18. Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia – lessons learned for prophylaxis
19. Menopause in Brazilian women with sickle cell anemia with and without hydroxyurea therapy
20. Deferasirox in patients with iron overload secondary to hereditary hemochromatosis: results of a 1-yr Phase 2 study
21. Pathophysiology and principles of management of the many faces of the acute vaso-occlusive crisis in patients with sickle cell disease
22. Clinical Utility of Lactate Dehydrogenase in Determining the Severity of Hemolysis in Sickle Cell Anemia
23. Deep venous thrombosis in children with sickle cell disease
24. Evidence gaps in the management of sickle cell disease: A summary of needed research
25. Climatic and geographic temporal patterns of pain in the Multicenter Study of Hydroxyurea
26. Stabilization of Erythrocyte Membranes by Polyamines
27. Costs to hospitals of acquiring and processing blood in the US: A survey of hospital-based blood banks and transfusion services
28. A predecessor of the current blood bank pneumatic tube delivery system
29. Management of Sickle Cell Disease: Summary of the 2014 Evidence-Based Report by Expert Panel Members
30. Thinking beyond sickling to better understand pain in sickle cell disease
31. Practice Guideline for Pulmonary Hypertension in Sickle Cell: Direct Evidence Needed before Universal Adoption
32. Treatment of the acute sickle cell vaso-occlusive crisis in the Emergency Department: a Brazilian method of switching from intravenous to oral morphine
33. Haemolysis and abnormal haemorheology in sickle cell anaemia
34. Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia
35. Time to rethink haemoglobin threshold guidelines in sickle cell disease
36. N-Terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease
37. Newborn Screening Program for Hemoglobinopathies in Rio De Janeiro, Brazil
38. Neuropathy, neuropathic pain, and sickle cell disease
39. Sickle Cell Anaemia: Progress in Pathogenesis and Treatment
40. Contributors
41. Sickle Cell Pain
42. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment
43. The first Cardeza donor center: attracting donors who do not wish to see blood
44. Sickle Cell Pain: Biology, Etiology, and Treatment
45. Iron nitrosyl hemoglobin formation from the reactions of hemoglobin and hydroxyurea
46. More definitions in sickle cell disease: Steady state v base line data
47. Opioids and Sickle Cell Disease: From Opium to the Opioid Epidemic
48. Determinants of the Outcome of the Transition of Children with Sickle Cell Disease to Adult Programs
49. Voxelotor Modulates the Analgesic Effect of Certain Opioids
50. AAAPT Diagnostic Criteria for Acute Sickle Cell Disease Pain
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