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1. Clinical and genetic characteristics of late-onset Huntington's disease

2. Identification of symbol digit modality test score extremes in Huntington's disease

3. Clinical manifestations of intermediate allele carriers in Huntington disease

4. Informing Carriers of ß-Thalassemia: Giving the Good News

5. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

6. Priapism in sickle-cell disease; incidence, risk factors and complications - an international multicentre study

7. Sickle cell disease

8. High prevalence of low bone mass in thalassaemia major

9. Combination therapy with interferon alpha and ribavirin for chronic hepatitis C virus infection in thalassaemic patients

10. Psychosocial and clinical burden of thalassaemia intermedia and its implications for prenatal diagnosis

11. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

12. A prospective diary study of stuttering priapism in adolescents and young men with sickle cell anemia: report of an international randomized control trial--the priapism in sickle cell study

14. Sleep Disordered Breathing And Transcranial Doppler In Sickle Cell Anaemia

15. Red cell deformability in oral contraceptive pill users with sickle cell anaemia

16. G410(P) Are adolescents with sickle cell disease satisfied with their out-patient clinic experience?

17. G409(P) An evaluation of the transition to adult care for young patients with sickle cell disease

18. The effects of neonatal screening for sickle cell disorders on lifetime treatment costs and early deaths avoided: a modelling approach

19. A home blood transfusion programme for beta-thalassaemia patients

20. Register cannot replace prospective studies in sickle cell disease

21. The effect of ovarian steroids on sickle cell deformability

22. The burden of poverty in children with haemoglobinopathies presenting to a London tertiary referral centre

23. Salmonella bacteraemia in children with sickle cell disease

24. Antibiotic sensitivity testing in enteric Salmonella

25. Low incidence of non-A, non-B post-transfusion hepatitis in London confirmed by hepatitis C virus serology

26. Hydroxyurea therapy for sickle cell disease in Britain

27. Genetic disease in the Arab world

28. The Safety and Pharmacokinetics of Deferitrin, a Novel Orally Available Iron Chelator

29. Platelet hyperaggregability occurring during prolonged continuous intravenous infusions of prostacyclin analogue ZK 36374

30. Clinical Management of Severe Sickle Cell Disease

31. SUCCESSFUL TREATMENT OF RAYNAUD'S SYNDROME WITH ILOPROST, A CHEMICALLY STABLE PROSTACYCLIN ANALOGUE

32. Detection of important abnormalities of the differential count using the Coulter STKR blood counter

33. The Cephalin Cholesterol Flocculation Test in Liver Disease

35. Clinical and Laboratory Observations on So-Called 'Kidney Threshold for Glucose'

36. Laboratory investigation of platelet function: a review of methodology

37. An evaluation of the Coulter VCS differential counter

38. Shoshin beriberi: an underdiagnosed condition?

39. Newer Pharmacological Agents

40. Incidence of endocrine complications and clinical disease severity related to genotype analysis and iron overload in patients with β- thalassaemia

41. Exchange transfusion and quinine concentrations in falciparum malaria

42. PAIN RELIEF IN SICKLE CELL CRISES

43. Diabetes Produced by Feeding Alloxan to Cats

45. PATHOGENESIS OF SO-CALLED DIFFUSE VASCULAR OR COLLAGEN DISEASE

46. PERIARTERITIS NODOSA WITH A CASE REPORT

47. PRIMARY CARCINOMA OF DUODENUM

48. PRIMARY HODGKIN'S DISEASE OF THE LUNG

49. PEPSIN IN THE PREVENTION OF ABDOMINAL ADHESIONS

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