Results 1 to 10 of about 21,388 (227)

Phenocopy syndrome of frontotemporal dementia

open access: yesEuropean Psychiatry, 2021
Introduction Frontotemporal dementia (FTD) is a group of neurodegenerative disorders characterized by behavioral or language changes with progressive executive dysfunction. It´s subdivided into two variants, the behavioral and language variants.
D. Martins   +3 more
doaj   +4 more sources

The role of autophagy in the pathogenesis and treatment of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) [PDF]

open access: yesAutophagy Reports
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) represent two extremes of a neurodegenerative disease spectrum characterised by overlapping genetic, clinical, and neuropathological features. This review covers the intricate relationship between both ALS and FTD and defects in the autophagy and endolysosomal pathway as recent ...
Jimmy Beckers, Philip Van Damme
exaly   +6 more sources

Co-morbid seizures in frontotemporal dementia: MRI and PET correlations [PDF]

open access: yesEpilepsy & Behavior Reports
Seizures are common in frontotemporal dementia (FTD). MRI and PET findings may provide valuable diagnostic insights for FTD patients with seizures, but are understudied.
Syeda Amrah Hashmi   +6 more
doaj   +2 more sources

Adaptación y validación de la Frontotemporal Dementia Rating Scale (FTD-FRS) al castellano [PDF]

open access: yesNeurología, 2017
Resumen: Introducción: La Frontotemporal Dementia Rating Scale (FTD-FRS) es una escala diseñada para facilitar la estadificación clínica y la evaluación de la progresión de pacientes con demencia frontotemporal (DFT).
O. Turró-Garriga   +7 more
doaj   +5 more sources

The Advance on Frontotemporal Dementia (FTD)'s Neuropathology and Molecular Genetics. [PDF]

open access: yesMediators Inflamm, 2022
The morbidity of frontotemporal dementia (FTD), one of the most prevalent dementias praccox, is second to Alzheimer disease (AD). It is different with AD that FTD has a rapider course and a higher mortality. FTD has not yet been fully understood in terms of etiology or pathogenesis, but genetic factors are believed to be involved.
Wang J, Wang B, Zhou T.
europepmc   +5 more sources

Discovery of cerebrospinal fluid biomarkers for different dementias using mass spectrometry‐based proteomics [PDF]

open access: yesAlzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
INTRODUCTION Common forms of dementia include Alzheimer's disease (AD), dementia with Lewy bodies (DLB), and frontotemporal dementia (FTD). Disease specific biomarkers are needed for differential disease diagnosis.
Marijke E. Stokkel   +13 more
doaj   +2 more sources

Adaptation and validation of a Spanish-language version of the Frontotemporal Dementia Rating Scale (FTD-FRS)

open access: yesNeurología (English Edition), 2017
Introduction: The Frontotemporal Dementia Rating Scale (FTD-FRS) is a tool designed to aid with clinical staging and assessment of the progression of frontotemporal dementia (FTD-FRS). Objective: Present a multicentre adaptation and validation study of a
O. Turró-Garriga   +7 more
doaj   +3 more sources

Chromosome 3 linked frontotemporal dementia (FTD-3)

open access: yesNeurology, 2002
Background: The authors have identified and studied a large kindred in which frontotemporal dementia (FTD) is inherited as an autosomal dominant trait. The trait has been mapped to the pericentromeric region of chromosome 3.
Gade, A   +13 more
core   +4 more sources

Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementia

open access: yesAlzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
INTRODUCTION We aimed to expand the range of the frontotemporal dementia (FTD) phenotypes assessed by the Clinical Dementia Rating Dementia Staging Instrument plus National Alzheimer's Coordinating Center Behavior and Language Domains (CDR plus NACC FTLD)
Kiran Samra   +34 more
doaj   +2 more sources

Immune Signaling Kinases in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). [PDF]

open access: yesInt J Mol Sci, 2021
Amyotrophic lateral sclerosis (ALS) is the most common neurodegenerative disorder of motor neurons in adults, with a median survival of 3–5 years after appearance of symptoms, and with no curative treatment currently available. Frontotemporal dementia (FTD) is also an adult-onset neurodegenerative disease, displaying not only clinical overlap with ALS,
García-García R   +4 more
europepmc   +7 more sources

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