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Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9pHormone replacement therapy and risk for neurodegenerative diseases.Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions.Progranulin deficiency induces overactivation of WNT5A expression via TNF-α/NF-κB pathway in peripheral cells from frontotemporal dementia-linked granulin mutation carriers.Atypical association of semantic dementia, corticobasal syndrome, and 4R tauopathy.Tau deletion impairs intracellular β-amyloid-42 clearance and leads to more extracellular plaque deposition in gene transfer models.Pazopanib Reduces Phosphorylated Tau Levels and Alters Astrocytes in a Mouse Model of Tauopathy.Beta-secretase inhibitors in phase I and phase II clinical trials for Alzheimer's disease.Intrafamilial Phenotypic Variability in the Gene Expansion: 2 Case Studies
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description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 11 October 2010
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetic causes of frontotemporal degeneration.
@en
Genetic causes of frontotemporal degeneration.
@nl
type
label
Genetic causes of frontotemporal degeneration.
@en
Genetic causes of frontotemporal degeneration.
@nl
prefLabel
Genetic causes of frontotemporal degeneration.
@en
Genetic causes of frontotemporal degeneration.
@nl
P2093
P2860
P356
P1476
Genetic causes of frontotemporal degeneration.
@en
P2093
Amanda K LaMarre
Suzee E Lee
Tricia M See
P2860
P304
P356
10.1177/0891988710383574
P577
2010-10-11T00:00:00Z