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Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid.
Acta Neuropathol ; 125(3): 463-5, 2013 Mar.
Article in En | MEDLINE | ID: mdl-23378033

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA-Binding Proteins / Frontotemporal Lobar Degeneration / Amyloid / Amyotrophic Lateral Sclerosis / Motor Cortex Limits: Humans Language: En Journal: Acta Neuropathol Year: 2013 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA-Binding Proteins / Frontotemporal Lobar Degeneration / Amyloid / Amyotrophic Lateral Sclerosis / Motor Cortex Limits: Humans Language: En Journal: Acta Neuropathol Year: 2013 Document type: Article