25 results for “frontotemporal”. Showing 25 of 39,449.
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.
frontotemporal dementia 'with definite frontotemporal lobar degeneration' requires histopathological confirmation
Advances and controversies in frontotemporal dementia: diagnosis, biomarkers, and therapeutic considerations.
frontotemporal dementia and frontotemporal lobar degeneration, with a much broader
Design considerations for C9orf72 disease prevention trials.
frontotemporal dementia has finally come of age. The hexanucleotide repeat
Intranasal oxytocin for apathy in people with frontotemporal dementia (FOXY): a multicentre, randomised, double-blind, placebo-controlled, adaptive, crossover, phase 2a/2b superiority trial.
frontotemporal dementia. Previously, in a randomised double-blind, placebo-controlled
Restoring neuronal progranulin reverses deficits in a mouse model of frontotemporal dementia.
frontotemporal dementia, a neurodegenerative disease commonly characterized by disrupted social
Reduction of sphingomyelinase activity associated with progranulin deficiency and frontotemporal dementia.
frontotemporal dementia. Progranulin mutations cause abnormalities in lysosomal lipid processing
Reduction of sphingomyelinase activity associated with progranulin deficiency and frontotemporal dementia.
frontotemporal dementia. Progranulin mutations cause abnormalities in lysosomal lipid processing
Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown.
frontotemporal dementia. As TMEM106B is a risk factor for frontotemporal
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.
frontotemporal dementia are extremely rare. We report a large family
Genetics of frontotemporal dementia in China.
frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), GRN and frontotemporal
Disease-modifying effects of TMEM106B in genetic frontotemporal dementia: a longitudinal GENFI study.
frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP). The G allele
A next-generation HDAC6 inhibitor for amyotrophic lateral sclerosis and frontotemporal dementia.
frontotemporal dementia. We present the pharmacological properties of EKZ-438, which
Frontotemporal Dementia: A Clinical Review.
Frontotemporal dementias are a clinically, neuroanatomically, and pathologically diverse group
Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations.
frontotemporal dementia. Most pathogenic GRN mutations result in progranulin haploinsufficiency
Plasma phosphorylated tau 217 and phosphorylated tau 181 as biomarkers in Alzheimer's disease and frontotemporal lobar degeneration: a retrospective diagnostic performance study.
frontotemporal lobar degeneration (FTLD) syndromes. In this retrospective multicohort diagnostic
Manganese-induced neurotoxicity and its role in frontotemporal dementia: Insights from the frontotemporal cortex of BALB/c mice.
Frontotemporal dementia (FTD) is a devastating neurological condition that causes
[Genetic Diversity in Frontotemporal Dementia].
Frontotemporal dementia is a progressive neurodegenerative disorder with high clinical
Glial reactivity and T cell infiltration in frontotemporal lobar degeneration with tau pathology.
Frontotemporal lobar degeneration with tau (FTLD-tau) is a group
Pharmacotherapy for Frontotemporal Dementia.
Frontotemporal dementia is a heterogeneous spectrum of neurodegenerative disorders. The neuropathological
Progranulin deficiency in the brain: the interplay between neuronal and non-neuronal cells.
frontotemporal dementia (FTD) with TAR DNA-binding protein 43 (TDP-43) inclusions
TAF15 amyloid filaments in frontotemporal lobar degeneration.
Frontotemporal lobar degeneration (FTLD) causes frontotemporal dementia (FTD), the most
Impairments of inhibitory neurons in amyotrophic lateral sclerosis and frontotemporal dementia.
frontotemporal dementia are two fatal neurodegenerative disorders. They are part
Clinical Subtypes of Frontotemporal Dementia.
Frontotemporal dementia (FTD) was one of the lesser known dementias
Recent Updates on the Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
frontotemporal dementia (FTD) primarily affect the motor and frontotemporal areas
Traumatic brain injury may increase the risk for frontotemporal dementia through reduced progranulin.
Frontotemporal lobar degeneration with TAR-DNA-binding protein inclusions (FTLD