Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders
The behavioural variant of frontotemporal dementia (bvFTD) is a frequent cause of early-
onset dementia. The diagnosis of bvFTD remains challenging because of the limited …
onset dementia. The diagnosis of bvFTD remains challenging because of the limited …
Frontotemporal dementia
J Bang, S Spina, BL Miller - The Lancet, 2015 - thelancet.com
Frontotemporal dementia is an umbrella clinical term that encompasses a group of
neurodegenerative diseases characterised by progressive deficits in behaviour, executive …
neurodegenerative diseases characterised by progressive deficits in behaviour, executive …
Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations
IR Mackenzie, T Arzberger, E Kremmer, D Troost… - Acta …, 2013 - Springer
Hexanucleotide repeat expansion in C9ORF72 is the most common genetic cause of
frontotemporal dementia and motor neuron disease. Recently, unconventional non-ATG …
frontotemporal dementia and motor neuron disease. Recently, unconventional non-ATG …
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis
C9orf72 hexanucleotide repeat expansions are the most common cause of familial
frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) worldwide. The …
frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) worldwide. The …
Network dysfunction in Alzheimer's disease and frontotemporal dementia: implications for psychiatry
Structural and functional connectivity methods are changing how researchers conceptualize
and explore neuropsychiatric disease. Here, we summarize emerging evidence of large …
and explore neuropsychiatric disease. Here, we summarize emerging evidence of large …
The clinical spectrum of sporadic and familial forms of frontotemporal dementia
IOC Woollacott, JD Rohrer - Journal of neurochemistry, 2016 - Wiley Online Library
The term frontotemporal dementia (FTD) describes a clinically, genetically and
pathologically diverse group of neurodegenerative disorders. Symptoms of FTD can present …
pathologically diverse group of neurodegenerative disorders. Symptoms of FTD can present …
Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype
DMA Mann, JS Snowden - Brain Pathology, 2017 - Wiley Online Library
Abstract Frontotemporal Lobar Degeneration (FTLD) is a clinically, pathologically and
genetically heterogeneous group of disorders that affect principally the frontal and temporal …
genetically heterogeneous group of disorders that affect principally the frontal and temporal …
The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype
Abstract The GGGGCC (G 4 C 2) repeat expansion in C9ORF72 is the most common cause
of familial amyotrophic lateral sclerosis (ALS), frontotemporal lobar dementia (FTLD) and …
of familial amyotrophic lateral sclerosis (ALS), frontotemporal lobar dementia (FTLD) and …
Heterozygous TREM2 mutations in frontotemporal dementia
A causative association was recently demonstrated between homozygous TREM2 mutations
and frontotemporal dementia (FTD)-like syndrome and between heterozygous TREM2 …
and frontotemporal dementia (FTD)-like syndrome and between heterozygous TREM2 …
Phenotypic heterogeneity of monogenic frontotemporal dementia
Frontotemporal dementia (FTD) is a genetically and pathologically heterogeneous disorder
characterized by personality changes, language impairment, and deficits of executive …
characterized by personality changes, language impairment, and deficits of executive …