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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Transl Psychiatry |
|---|---|
| Prif Awduron: | , , , , , , , , , , , , , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Nature Publishing Group UK
2019
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| Pynciau: | |
| 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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