Cargando…
Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process
Prion diseases are a group of rare neurodegenerative conditions characterised by a high rate of progression and highly heterogeneous phenotypes. Whilst the most common form of prion disease occurs sporadically (sporadic Creutzfeldt–Jakob disease, sCJD), other forms are caused by prion protein gene m...
Autores principales: | Canas, Liane S., Sudre, Carole H., De Vita, Enrico, Nihat, Akin, Mok, Tze How, Slattery, Catherine F., Paterson, Ross W., Foulkes, Alexander J.M., Hyare, Harpreet, Cardoso, M. Jorge, Thornton, John, Schott, Jonathan M., Barkhof, Frederik, Collinge, John, Ourselin, Sébastien, Mead, Simon, Modat, Marc |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978211/ https://www.ncbi.nlm.nih.gov/pubmed/31734530 http://dx.doi.org/10.1016/j.nicl.2019.102051 |
Ejemplares similares
-
Assessing initial MRI reports for suspected CJD patients
por: Jesuthasan, Aaron, et al.
Publicado: (2022) -
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseases
por: Hyare, Harpreet, et al.
Publicado: (2020) -
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases
por: Mok, Tze How, et al.
Publicado: (2021) -
Enteral feeding is associated with longer survival in the advanced stages of prion disease
por: McNiven, Kirsty, et al.
Publicado: (2019) -
Imaging and CSF analyses effectively distinguish CJD from its mimics
por: Rudge, Peter, et al.
Publicado: (2018)