Results 131 to 140 of about 30,886 (249)
Comparison of Magnetic Resonance Spectra Acquired With Hybrid PET/MR and Standalone MR Scanners
ABSTRACT Background The effect of the positron emission tomography (PET) modality in hybrid PET/MR scanners on MR spectral quality is unclear. Purpose To evaluate spectral quality, quantification, and repeatability of brain MR spectroscopy (MRS) acquired on PET/MR and standalone MR scanners. Study Type Prospective.
Carter B. Macdonald +6 more
wiley +1 more source
Novel diagnostic cerebrospinal fluid biomarkers for pathologic subtypes of frontotemporal dementia identified by proteomics [PDF]
Introduction: Reliable cerebrospinal fluid (CSF) biomarkers enabling identification of frontotemporal dementia (FTD) and its pathologic subtypes are lacking.
Beccari, T. (Tommaso) +12 more
core +1 more source
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration [PDF]
Sonia Bellini +17 more
openalex +1 more source
MRI‐DTI Biomarkers Along the Continuum of Behavioral Variant Frontotemporal Dementia
ABSTRACT Background We investigated whether diffusion tensor imaging (DTI) and atlas‐based volumetry (ABV) could track specific patterns of brain white matter (WM) microstructure and gray matter (GM) volumes in behavioral variant frontotemporal dementia (bvFTD) and amyotrophic lateral sclerosis with frontotemporal dementia (ALS‐FTD).
Marco Michelutti +13 more
wiley +1 more source
Objectives: To explore the relationship between severe/serious mental illness (SMI) and the behavioral variant of frontotemporal dementia (bvFTD), as the patterns of symptoms and cognitive performance that characterize both disorders share similarities.
Leandro Boson Gambogi +3 more
doaj +1 more source
Atypical Frontotemporal Dementia Associated With SQSTM1 Gene Mutation: A Clinicopathological Case
ABSTRACT A 78‐year‐old man presented with a six‐year history of progressive memory decline, initially manifesting as recent memory impairment and mild anomia, which gradually evolved into motor clumsiness, gait disturbances, language difficulties, behavioral changes, and late‐onset parkinsonism. He had been diagnosed with Paget disease of bone (PDB) at
Christian Espinoza‐Vinces +8 more
wiley +1 more source
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 functions associated with frontal and temporal lobe degeneration.
Alberto eBenussi +2 more
doaj +1 more source
A Case of Frontotemporal Lobar Degeneration with Progressive Dysarthria
We investigated the evolution of the neurological and neuropsychological characteristics in a right-handed woman who was 53-years-old at the onset and who showed personality changes and behavioral disorders accompanied by progressive dysarthria.
Nami Ihori +3 more
doaj +1 more source
Loss-of-function mutations affecting the lysosomal protein progranulin are a leading cause of frontotemporal dementia. Progranulin mutations cause abnormalities in lysosomal lipid processing, particularly of sphingolipids, major components of neural cell
Nicholas R. Boyle +12 more
doaj +1 more source

