Cognitive inhibition impairments in presymptomatic C9orf72 carriers
نویسندگان
چکیده
منابع مشابه
Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers
Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis. Previous work has shown that patients with behavioral variant frontotemporal dementia due to C9ORF72 show salience and sensorimotor network disruptions comparable to those seen in sporadic behavioral variant frontotemporal dement...
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350 words) Importance: Presymptomatic carriers of c9orf72 mutation, the most frequent genetic cause of FLTD and ALS, represent the optimal target population for the development of diseasemodifying drugs. Preclinical biomarkers are needed in order to monitor the effect of therapeutic interventions in this population. Objectives: To assess the occurrence of cognitive, structural and microstructur...
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ژورنال
عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry
سال: 2020
ISSN: 0022-3050,1468-330X
DOI: 10.1136/jnnp-2019-322242