A new variant of Creutzfeldt-Jakob disease in the UK
- 6 April 1996
- journal article
- research article
- Published by Elsevier BV in The Lancet
- Vol. 347 (9006), 921-925
- https://doi.org/10.1016/s0140-6736(96)91412-9
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)Brain Pathology, 1995
- Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob diseaseNeuroscience Letters, 1995
- Creutzfeldt-Jakob disease in young peopleEuropean Journal of Epidemiology, 1991
- The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesisJournal of General Virology, 1991
- Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84.Journal of Neurology, Neurosurgery & Psychiatry, 1990
- Progressive Neurological Deterioration in a 14-Year-Old GirlPediatric Neurosurgery, 1988
- The epidemiology of Creutzfeldt‐Jakob diseaseNeurology, 1987
- Epidemiologic implications of Creutzfeldt-Jakob disease in a 19 year-old girlEuropean Journal of Epidemiology, 1985
- Creutzfeldt-Jakob disease in an adolescentJournal of the Neurological Sciences, 1981
- Creutzfeldt‐Jakob disease in a 20‐year‐old womanNeurology, 1980