25 results for “ftd”. Showing 25 of 39,449.
Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup.
FTD) are currently lacking. FTD may be associated with chronic
Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations.
FTD with GRN (FTD-GRN) or C9orf72 (FTD-C9orf72) gene
Frontotemporal dementia patient-derived iPSC neurons show cell pathological hallmarks and evidence for synaptic dysfunction and DNA damage.
FTD patients recapitulate pathological changes of the FTD brain and strongly
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit.
FTD) and amyotrophic lateral sclerosis (ALS; C9ORF72-FTD/ALS). The goal
An update on genetic frontotemporal dementia.
FTD. Age at symptom onset in genetic FTD is variable
Update on Disease-Modifying Pharmacological Treatments for Frontotemporal Dementia (FTD): A Scoping Review of Registered Trials.
FTD targeting neuroinflammation, the PEA-FTD and C9orf72 ALS/FTD trials
Frontotemporal Dementia.
FTD) syndromes using a simplified framework of three core syndromes
Neurovascular dysfunction in GRN-associated frontotemporal dementia identified by single-nucleus RNA sequencing of human cerebral cortex.
FTD (FTD-GRN), associated with TDP-43 inclusions, neuronal loss
New Approaches to the Treatment of Frontotemporal Dementia.
FTD) comprises a diverse group of clinical neurodegenerative syndromes characterized
Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations.
FTD patients, 61 (23.4%) carried potential causative variants in FTD
Progranulin and TMEM106B: when two become wan.
FTD). FTD is a devastating disease characterised by neuronal loss
A single-cell, long-read, isoform-resolved case-control study of FTD reveals cell-type-specific and broad splicing dysregulation in human brain.
FTD) is a major cause of familial FTD with TAR DNA-binding
Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Have Distinct Prediagnostic Blood Biochemical Profiles.
FTD. Research in monogenic ALS and FTD is needed to determine
Changes in the public IgM repertoire and its idiotypic connectivity in Alzheimer's disease and frontotemporal dementia.
FTD) are prevalent neurodegenerative disorders. Early diagnosis is challenging due to the lack
Genetics of frontotemporal dementia in China.
FTD may be different. Methods: To explore the genetics of FTD
Parkinsonism, movement disorders and genetics in frontotemporal dementia.
FTD) refers to a group of clinically and genetically heterogeneous
Frontotemporal Dementia: A Cross-Cultural Perspective.
FTD) may have a worldwide distribution; however, data available on their
Advances in Treatment of Frontotemporal Dementia.
FTD), focusing on treatment. The clinical features of FTD are unique
Plasma lipidome dysregulation in frontotemporal dementia reveals shared, genotype-specific, and severity-linked alterations.
FTD (GRN, C9orf72, MAPT) and non-carriers. RESULTS: FTD subjects
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia.
FTD) is the form of neurodegenerative dementia with the highest
Psychosis in frontotemporal dementia.
FTD) is a neurodegenerative disorder, associated with a progressive decline
Impaired protein degradation in FTLD and related disorders.
FTD. Furthermore, the strongest evidence for lysosomal impairment in FTD
Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum.
FTD) and amyotrophic lateral sclerosis (ALS). Perturbed SG dynamics appears
Osteopontin drives neuroinflammation and cell loss in MAPT-N279K frontotemporal dementia patient neurons.
FTD. We identified disease phenotypes in FTD neurons carrying the MAPT
A Systematic Review of the Genetics and Pathology of Psychosis in Frontotemporal Dementia.
FTD, and in the different pathological subtypes of FTD. We conducted