The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

BACKGROUND: Creutzfeldt-Jakob Disease (CJD) is the most common prion disease in humans causing a rapidly progressive neurological decline and dementia and is invariably fatal. The familial forms (genetic CJD, gCJD) are caused by mutations in the PRNP gene encoding for the prion protein (PrP). In Isr...

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Detalles Bibliográficos
Autores principales: Bregman, Noa, Shiner, Tamara, Kavé, Gitit, Alcalay, Roy, Gana-Weisz, Mali, Goldstein, Orly, Glinka, Tal, Aizenstein, Orna, Bashat, Dafna Ben, Alcalay, Yifat, Mirelman, Anat, Thaler, Avner, Giladi, Nir, Omer, Nurit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108539/
https://www.ncbi.nlm.nih.gov/pubmed/37069531
http://dx.doi.org/10.1186/s12883-023-03193-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108539/
https://www.ncbi.nlm.nih.gov/pubmed/37069531
http://dx.doi.org/10.1186/s12883-023-03193-8

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