476 results on '"Will, R G"'
Search Results
2. Clinical Features of Variant Creutzfeldt-Jakob Disease
3. The Epidemiology of Variant Creutzfeldt-Jakob Disease
4. Isolated language impairment as the primary presentation of sporadic Creutzfeldt Jakob Disease
5. Incidence of Creutzfeldt-Jakob Disease in the European Community
6. Creutzfeldt–Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study
7. Vcjd: The Epidemic That Never Was
8. Diagnosis of Creutzfeldt-Jakob Disease
9. Epidemiological Surveillance of Creutzfeldt-Jakob Disease in the United Kingdom
10. New Variant Creutzfeldt-Jakob Disease Is More Common in Britain than Elsewhere
11. Sporadic Creutzfeldt-Jakob Disease in the United Kingdom: Analysis of Epidemiological Surveillance Data for 1970-96
12. Creutzfeldt-Jakob Disease And Bovine Spongiform Encephalopathy
13. Variant CJD and blood transfusion: are there additional cases?
14. Postmortem findings in a case of variant Creutzfeldt-Jakob disease treated with intraventricular pentosan polysulfate
15. Human prion diseases
16. Diagnosing variant Creutzfeldt–Jakob disease: a retrospective analysis of the first 150 cases in the UK
17. The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt–Jakob disease in the UK: a 10-year review
18. Genetic Creutzfeldt–Jakob disease mimicking variant Creutzfeldt–Jakob disease
19. Variant Creutzfeldt-Jakob disease and exposure to fractionated plasma products
20. A retrospective case note review of deceased recipients of vCJD-implicated blood transfusions
21. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
22. The first case of variant Creutzfeldt-Jakob disease in the Netherlands
23. MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement study
24. Unsuccessful intraventricular pentosan polysulphate treatment of variant Creutzfeldt-Jakob disease
25. Sporadic Creutzfeldt–Jakob disease in two adolescents
26. Causes of progressive intellectual and neurological deterioration in UK children: findings of a prospective national study after almost 10 years of surveillance: B: 8
27. Sporadic Creutzfeldt–Jakob disease with cerebellar ataxia at onset in the UK
28. Three reported cases of variant Creutzfeldt–Jakob disease transmission following transfusion of labile blood components
29. Creutzfeldt–Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review study
30. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt–Jakob disease
31. Dura mater-associated Creutzfeldt–Jakob disease: experience from surveillance in the UK
32. No clinical evidence of hidden vCJD in UK children
33. Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the “Heidenhain variant”
34. Inaugural national scientific medical meeting
35. Oral Infection by the Bovine Spongiform Encephalopathy Prion
36. Predictors of survival in sporadic Creutzfeldt–Jakob disease and other human transmissible spongiform encephalopathies
37. New variant Creutzfeldt–Jakob disease: FW6-2
38. Is variant Creutzfeldt-Jakob disease in young children misdiagnosed as Alpers’ syndrome? An analysis of a national surveillance study
39. Ophthalmic surgery and Creutzfeldt-Jakob disease
40. PRION DISEASES
41. Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND)
42. The clinical spectrum of peripheral neuropathies associated with benign monoclonal IgM, IgG and IgA paraproteinaemia: Comparative clinical, immunological and nerve biopsy findings
43. The neuropsychological profile associated with variant Creutzfeldt–Jakob disease
44. Progress with Prions
45. Update on the vCJD scene
46. Variant Creutzfeldt-Jakob disease: How new is new?
47. Variant Creutzfeldt-Jakob disease is not associated with individual abilities to metabolise organophosphates
48. Use of 14–3–3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease
49. Variant Creutzfeldt-Jakob disease in UK children: a national surveillance study
50. Incidence of variant Creutzfeldt-Jakob disease in the UK
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