FDG-PET underscores the key role of the thalamus in frontotemporal lobar degeneration caused by C9ORF72 mutations

C9ORF72 mutations are the most common cause of familial frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). MRI studies have investigated structural changes in C9ORF72-associated FTLD (C9FTLD) and provided first insights about a prominent involvement of the thalamus and...

Descripción completa

Detalles Bibliográficos
Autores principales: Diehl-Schmid, Janine, Licata, Abigail, Goldhardt, Oliver, Förstl, Hans, Yakushew, Igor, Otto, Markus, Anderl-Straub, Sarah, Beer, Ambros, Ludolph, Albert Christian, Landwehrmeyer, Georg Bernhard, Levin, Johannes, Danek, Adrian, Fliessbach, Klaus, Spottke, Annika, Fassbender, Klaus, Lyros, Epameinondas, Prudlo, Johannes, Krause, Bernd Joachim, Volk, Alexander, Edbauer, Dieter, Schroeter, Matthias Leopold, Drzezga, Alexander, Kornhuber, Johannes, Lauer, Martin, Grimmer, Timo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355852/
https://www.ncbi.nlm.nih.gov/pubmed/30705258
http://dx.doi.org/10.1038/s41398-019-0381-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355852/
https://www.ncbi.nlm.nih.gov/pubmed/30705258
http://dx.doi.org/10.1038/s41398-019-0381-1

Ejemplares similares