… , with mutations more rarely seen in a number of other genes. This review will discuss the …
of genetic FTD. Age at symptom onset in genetic FTD is variable with recently identified genetic …

… Rare defects in VCP, CHMP2B, TARDP and FUS genes … neuron disease, although the
causative gene is yet to be identified. … , imaging, genetic and pathological developments that have …

… Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia
in the genetic frontotemporal dementia initiative (GENFI) study: a cross-sectional analysis. …

… dominant genetic mutations usually in one of three genes: … Findings from studies of other
genetic dementias have shown … such changes could be shown in frontotemporal dementia. …

… genetic variations for frontotemporal dementia? Findings In this cohort study of 232 patients
with genetic frontotemporal dementia, … the common frontotemporal dementia gene variations …

… Conclusion: Future genetic studies need to identify genetic defects in at least two distinct
familial forms of frontotemporal dementia (FTD) with unknown genetic defects: frontotemporal …

… frontotemporal dementia (FTD) have an autosomal dominant pattern of inheritance. Genetic
FTD is caused by mutations in three genes in most … a number of other genes are rare causes. …

… immunoreactivity in frontotemporal dementia with … in frontotemporal dementia with ubiquitin
inclusions (B), and dense and granular tau immunoreactivity in frontotemporal dementia with …

… of a genetic mutation in the C9orf72 gene, the most common mutation found to be causative
of sporadic and familial frontotemporal … In this review, we will discuss the current genetic and …

… Mutations in the gene MAPT on chromosome 17 have been found to be associated with
Pick … Genetic and idiopathic forms of FTD have similar imaging and genetic mutations, sug…