95 results on '"Rees, David"'
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2. White matter integrity and processing speed in sickle cell anemia
3. Are the risks of treatment to cure a child with severe sickle cell disease too high?
4. How I manage red cell transfusions in patients with sickle cell disease
5. Supplement to: A multinational trial of prasugrel for sickle cell vasoocclusive events.
6. Are the risks of treatment to cure a child with severe sickle cell disease too high?
7. The super sickling haemoglobin HbS‐Oman: a study of red cell sickling, K+ permeability and associations with disease severity in patients heterozygous for HbA and HbS‐Oman (HbA/S‐Oman genotype)
8. Update review of the acute porphyrias
9. Update review of the acute porphyrias
10. Follicular variant of papillary thyroid carcinoma: an unusual cause of thyrotoxicosis
11. Longitudinal assessment of lung function in children with sickle cell disease
12. Patent ductus arteriosus illuminating an old eponym
13. A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive Events
14. Design of the DOVE (Determining Effects of Platelet Inhibition on Vaso-Occlusive Events) trial: A global Phase 3 double-blind, randomized, placebo-controlled, multicenter study of the efficacy and safety of prasugrel in pediatric patients with sickle cell anemia utilizing a dose titration strategy
15. Autoimmune Liver Disease in Children with Sickle Cell Disease
16. 13-valent pneumococcal conjugate vaccine (PCV13) is immunogenic and safe in children 6–17 years of age with sickle cell disease previously vaccinated with 23-valent pneumococcal polysaccharide vaccine (PPSV23): Results of a phase 3 study
17. Emergency department noise: mental activation or mental stress?
18. Investigating the effectiveness of occupational health interventions in the workplace
19. Effects of 5-hydroxymethyl-2-furfural on the volume and membrane permeability of red blood cells from patients with sickle cell disease
20. Airways obstruction and pulmonary capillary blood volume in children with sickle cell disease
21. The spleen and sickle cell disease: the sick(led) spleen
22. Management of sickle cell disease in the community
23. Cost-effectiveness analysis of preoperative transfusion in patients with sickle cell disease using evidence from the TAPS trial
24. Nontraumatic extradural hematoma in sickle cell anemia: a rare neurological complication not to be missed
25. Urinary excretion of porphyrins, porphobilinogen and δ-aminolaevulinic acid following an attack of acute intermittent porphyria
26. Combined blood transfusion and hydroxycarbamide in children with sickle cell anaemia
27. The acute porphyrias
28. Self-assessment questions: The acute porphyrias
29. Discovery of AT26893, a novel allosteric inhibitor of the regulation of HCV NS3/4a protein function: 1903
30. Discovery of a novel allosteric mechanism for the regulation of HCV NS3/4a protein function present across all genotypes: 1069
31. A ‘whole of system’ approach to compare options for CVD interventions in Counties Manukau
32. Biomarkers in sickle cell disease
33. Biomarkers in sickle cell disease
34. Portacaths are safe for long-term regular blood transfusion in children with sickle cell anaemia
35. The safety and efficacy of hydroxycarbamide in infants with sickle cell anemia
36. Respirable Dust and Quartz Exposure from Three South African Farms with Sandy, Sandy Loam, and Clay Soils
37. Inheritance of Flowering Time in Apricot (Prunus armeniaca L.) and Analysis of Linked Quantitative Trait Loci (QTLs) using Simple Sequence Repeat (SSR) Markers
38. Soluble CD163 levels in children with sickle cell disease
39. ENERCA clinical recommendations for disease management and prevention of complications of sickle cell disease in children
40. A retrospective analysis of outcome of pregnancy in patients with acute porphyria
41. Outcome of children with sickle cell disease admitted to intensive care – a single institution experience
42. Outcome of adults with sickle cell disease admitted to critical care – experience of a single institution in the UK
43. Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene
44. Calcinosis in juvenile dermatomyositis
45. Acute human parvovirus B19 infection and nephrotic syndrome in patients with sickle cell disease
46. Significant haemoglobinopathies: guidelines for screening and diagnosis
47. Quartz Exposure in Agriculture: Literature Review and South African Survey
48. Oscillating Migration and the Epidemics of Silicosis, Tuberculosis, and HIV Infection in South African Gold Miners
49. Transport of Electrons on Liquid Helium Across a Tunable Potential Barrier in a Point Contact-like Geometry
50. Stroke prevention in the young child with sickle cell anaemia
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