152 results on '"Telfer, Paul"'
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2. Exagamglogene Autotemcel for Severe Sickle Cell Disease
3. The acute pain crisis in sickle cell disease: What can be done to improve outcomes?
4. Elimination of Vaso-Occlusive Crises after Exagamglogene Autotemcel in Patients with Severe Sickle Cell Disease
5. Haematopoietic stem cell health in sickle cell disease and its implications for stem cell therapies and secondary haematological disorders
6. P1441: REAL-WORLD OUTCOMES AND DIGITALLY MONITORED QUALITY OF LIFE IN CRIZANLIZUMAB-TREATED PATIENTS WITH SICKLE CELL DISEASE.
7. P1448: CHARACTERISATION OF QUALITY OF LIFE-LINKED PATIENT-REPORTED OUTCOMES THROUGH A DIGITAL AND CONTINUOUS REMOTE MONITORING ECOSYSTEM IN SICKLE CELL DISEASE.
8. P1428: PREDICTORS OF VOC RATE DURING LONG-TERM FOLLOW-UP OF PATIENTS WITH HBSS IN A NEWBORN COHORT STUDY
9. Efficacy, safety, and pharmacokinetics of a new, ready-to-use, liquid hydroxyurea in children with sickle cell anemia
10. Direct correction of haemoglobin E β-thalassaemia using base editors
11. Genetic solutions through breeding counteract climate change and secure barley production in Australia
12. A multi-environment framework to evaluate the adaptation of wheat (Triticum aestivum) to heat stress
13. Sickle Cell Disease in Clinical Practice
14. Long-Term Safety and Efficacy of Voxelotor for Patients with Sickle Cell Disease: Results from an Open-Label Extension of the Phase 3 HOPE Trial
15. Severe Acute Complications of Sickle Cell Disease in Two Expert Referral Centers (UK and Italy): Natural History Studies Highlight Ongoing Unmet Need for Effective Disease Modifying or Curative Therapies
16. A Multi-environment Framework to Evaluate the Adaptation of Wheat (Triticum Aestivum) to Heat Stress
17. Routine management, healthcare resource use and patient and carer‐reported outcomes of patients with transfusion‐dependent β‐thalassaemia in the United Kingdom: A mixed methods observational study
18. Neurological Complications
19. Overview and General Principles
20. Anemia and Sickle Cell Disease
21. Renal and Urological Complications
22. Laboratory Tests Used in Diagnosis and Monitoring
23. The Spleen
24. Treatment of Sickle Cell Disease
25. Infection and Infection Prophylaxis
26. Out-Patient Management
27. Pain in Sickle Cell Disease
28. Leg Ulceration
29. Respiratory and Cardiac Complications
30. Surgical Management
31. Bone and Joint Complications in Sickle Cell Disease
32. Ophthalmological Complications
33. Gastroenterological Complications
34. Organization of Care
35. Overview of Sickle Cell Disease
36. Management of Pregnancy
37. A non-injected opioid analgesia protocol for acute pain crisis in adolescents and adults with sickle cell disease
38. The parental perspective of thalassaemia in Bangladesh: lack of knowledge, regret, and barriers
39. The Parental Perspective of Thalassaemia in Bangladesh: Lack of knowledge, Regret, and Barriers
40. Salvage of refractory post‐transfusion hyperhaemolysis by targeting hyperinflammation and macrophage activation with tocilizumab
41. Genetic analysis of wheat (Triticum aestivum) adaptation to heat stress
42. The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editing
43. Improvement in the Clinical Global Impression of Change with Voxelotor in Patients with Sickle Cell Disease in the Phase 3 HOPE Trial
44. Higher Hemoglobin Levels Achieved with Voxelotor Are Associated with Lower Vaso-occlusive Crisis Incidence: 72-Week Analysis from the HOPE Study
45. Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis
46. Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients
47. Evaluation of the efficacy and safety of deferiprone compared with deferasirox in paediatric patients with transfusion-dependent haemoglobinopathies (DEEP-2): a multicentre, randomised, open-label, non-inferiority, phase 3 trial
48. Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): study protocol for a randomised controlled feasibility trial
49. Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study
50. Not being heard: barriers to high quality unplanned hospital care during young people’s transition to adult services – evidence from ‘this sickle cell life’ research
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