434 results on '"Lee, C."'
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2. Third Åland islands conference on von Willebrand disease, 26–28 September 2012: meeting report
3. The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products
4. Joint protection in haemophilia
5. First 20 years with recombinant FVIIa (NovoSeven)
6. Secondary prophylaxis treatment versus on-demand treatment for patients with severe haemophilia A: comparisons of cost and outcomes in Taiwan
7. The effects of mode of delivery, maternal and fetal factors on the coagulation system in the term neonate: 36P06
8. Commentary on Brackmann and Gormsen (Lancet 1977; ii: 933): Massive factor-VIII infusion in haemophiliac with factor-VIII inhibitor, high responder
9. Risk reduction strategies for variant Creutzfeldt–Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders
10. Current approaches in haemophilic arthropathy of the hip
11. Bleeding and clotting: new therapies and old issues revisited1
12. Ankle arthropathy in the haemophilic patient: a description of a novel ankle arthrodesis technique
13. Review of a multidisciplinary clinic for women with inherited bleeding disorders
14. Haemophilia: January 2009
15. Prevention of arthropathy in haemophilia – intensive on-demand treatment, UK perspective
16. Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors?
17. Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency
18. Carrier testing in haemophilia A and B: adult carriersʼ and their partnersʼ experiences and their views on the testing of young females
19. Best practice: protecting research subjects, patients and experimental animals
20. Pregnancy in carriers of haemophilia
21. Coagulation deficiencies: a look to the future
22. Prevention of haemophilic synovitis: prophylaxis
23. An outline of the current orthopaedic management of haemophilic disease of the upper limb
24. Parents of children with haemophilia – a transforming experience
25. Is primary postpartum haemorrhage a good predictor of inherited bleeding disorders?
26. Pharmacokinetic studies in patients with inherited bleeding disorders – challenges and relevance to clinical practice
27. Heterotropic bone formation as a complication of elective joint replacement in haemophilic patients – a case report and literature review
28. Screening for factor XI deficiency amongst pregnant women of Ashkenazi Jewish origin
29. The 80th anniversary of von Willebrandʼs disease: history, management and research
30. Coagulation deficiencies: a look to the future
31. Identification and management of women with inherited bleeding disorders: a survey of obstetricians and gynaecologists in the United Kingdom
32. Pregnancy in women with congenital factor VII deficiency
33. The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctorsʼ Organization
34. Factor VIII and VWF levels in cord blood of healthy full term neonates: effect of labour, mode of delivery and fetal sex: 31 PO 946
35. Study of changes in factor VIII and Von Willebrand Factor levels in intrapartum and postpartum period in normal pregnancy: 31 PO 947
36. Intrapartum pain relief in women with inherited bleeding disorders: 31 FP 939
37. Obstetric experience of women with factor XI deficiency: 26 PO 831
38. ʼSo whatʼs the problem?ʼ Constructing life positively around haemophilia: 25 S 792
39. What are the future issues that parents of children affected by haemophilia A and B think about most?: 24 FP 749
40. Evaluation of total knee replacements - two case studies: 18 PO 541
41. A retrospective review of factor XI concentrate (BPL®) use in surgery: single centre experience, 1995-000: 05 PO 120
42. Disorders of menstruation and their effect on the quality of life in women with congenital factor VII deficiency
43. Current issues facing coagulationists – meeting report
44. Ortner syndrome and haemophilia
45. An exploration of health-related quality of life in adults with haemophilia – a qualitative perspective
46. OnlineEarly Announcement
47. The evaluation of health related quality of life in adults with haemophilia
48. Twenty years experience of total knee arthroplasty in end-stage haemophilic arthropathy
49. An evaluation of quality of life for parents of children with severe haemophilia
50. Comparative study of full-length and B-domain deleted factor VIII concentrates
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