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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Publicado no:Transl Psychiatry
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Article
Acesso em linha: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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