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pro vyhledávání: '"H J T Ward"'
Autor:
M Bain, H J T Ward
Publikováno v:
Scottish medical journal. 59(1)
Background and aims Assessing the contribution of ‘support services’ to improving healthcare is challenging. Despite involving a significant part of the NHS budget, there is very little published literature on methods and approaches. This article
Autor:
A, Peden, L, McCardle, M W, Head, S, Love, H J T, Ward, S N, Cousens, D M, Keeling, C M, Millar, F G H, Hill, J W, Ironside
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(2)
All UK patients with bleeding disorders treated with any UK-sourced pooled factor concentrates between 1980 and 2001 have been informed that they may be at an increased risk of infection with variant Creutzfeldt-Jakob disease (vCJD). We describe a st
Autor:
H J T Ward
Publikováno v:
Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 11(6)
There is now evidence that a new human genotype is susceptible to variant Creutzfeldt-Jakob disease
Autor:
R G, Will, H J T, Ward
Publikováno v:
Current topics in microbiology and immunology. 284
The possibility that a new form of human prion disease, variant Creutzfeldt-Jakob disease (vCJD) had occurred in the UK was first raised by the identification of a small number of cases with unusual clinical characteristics. Atypical features include
Publikováno v:
Current topics in microbiology and immunology. 284
Variant Creutzfeldt-Jakob disease (vCJD) was identified as a new disease in 1996. It was linked to infection with the bovine spongiform encephalopathy (BSE) agent although the epidemiological evidence for this was not strong, but later strain typing
Autor:
H J T Ward
Publikováno v:
Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 5(9)
By the end of May 2000, 54 definite cases and 13 probable cases of vCJD had been notified in the United Kingdom by the National CJD Surveillance Unit set up in 1990. All definite cases for whom data are available are methionine homozygous at codon 12