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A transmissible spongiform encephalopathy of cattle associated with abnormal prion proteins in the brain. Affected animals develop excitability and salivation followed by ATAXIA. This disorder has been associated with consumption of SCRAPIE infected ruminant derived protein. This condition may be transmitted to humans, where it is referred to as variant or new variant CREUTZFELDT-JAKOB SYNDROME. (Vet Rec 1998 Jul 25;143(41):101-5)
View Complete DescriptionAuthors: Corinne Ida Lasmézas, Emmanuel Comoy, Stephen Hawkins, Christian Herzog, Franck Mouthon, Timm Konold, Frédéric Auvré, Evelyne Correia, Nathalie Lescoutra-Etchegaray, Nicole Salès,…
Lancet 2005 Feb 26-Mar 4Authors: Alan C F Colchester, Nancy T H Colchester
Lancet 2005 Sep 3-9Thought leaders and organizations working on research involving Bovine Spongiform Encephalopathy.
conditions: Prion Disease
interventions: Quinacrine
conditions: DiGeorge Anomaly
interventions: Serum Free Thymus Transplantation with Immunosuppression ; Serum Free Thymus Transplantation without immunosuppression
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