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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Transl Psychiatry
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group UK 2019
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6355852/
https://ncbi.nlm.nih.gov/pubmed/30705258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-019-0381-1
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