Search Results

Disease-related cortical thinning in presymptomatic granulin mutation carriers

• Authors : Borrego-Écija, Sergi; Sala-Llonch, Roser; van Swieten, John

Subjects: Frontotemporal dementia; Cortical thickness; GRN

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A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study.

• Authors : Bergström, Sofia; Öijerstedt, Linn; Finger, Elizabeth

Subjects: info:eu-repo/classification/ddc/570; Biomarkers; BrainDE

• Source: Molecular neurodegeneration 16(1), 79 (2021). doi:10.1186/s13024-021-00499-4

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Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers

• Authors : Finger, Elizabeth; Malik, Rubina; Bocchetta, Martina ...

Subjects: Adult; C9orf72 Protein; neurodevelopment

• Source: BrainBrain : a journal of neurology, 146(5), 2120-2131. Oxford University PressBrain 146(5), 2120-2131 (2023). doi:10.1093/brain/awac446

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Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations

• Authors : Bouzigues, Arabella; Russell, Lucy L; Tiraboschi, Pietro ...

Subjects: Progranulin; Clinical Neurology; Medizin

• Source: Neuroscience Institute PublicationsJournal of neurologyJournal of neurology 269(8), 4322-4332 (2022). doi:10.1007/s00415-022-11068-0Journal of Neurology, 269(8), 4322-4332. D.

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The CBI-R detects early behavioural impairment in genetic frontotemporal dementia

• Authors : Nelson, Annabel; Russell, Lucy L.; Moreno, Fermin ...

Subjects: FUNCTIONAL BRAIN CONNECTIVITY; Clinical Neurology; Medizin

• Source: Annals of Clinical and Translational Neurology, 9(5), 644-658. John Wiley & Sons Inc.Genetic FTD Initiative (GENFI) 2022, ' The CBI-R detects early behavioural impairment in genetic

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Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia

• Authors : Heller, Carolin; Foiani, Martha S; Shafei, Rachelle ...

Subjects: blood [Frontotemporal Dementia]; Male; blood [Neurofilament Proteins]

• Source: Medical Biophysics PublicationsJournal of Neurology, Neurosurgery and Psychiatry, 91(3):2019321954. BMJ Publishing GroupRepositório Científico de Acesso Aberto de Portugal

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The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort

• Authors : Franklin, Hannah D; Russell, Lucy L; Jiskoot, Lize ...

Subjects: Social Cognition; Neurology; Medizin

• Source: Alzheimer's Research & TherapyAlzheimer's research & therapy 13(1), 127 (2021). doi:10.1186/s13195-021-00865-wRepositório Científico de Acesso Aberto de PortugalRepositório

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Differential early subcortical involvement in genetic FTD within the GENFI cohort

• Authors : Bocchetta, Martina; Todd, Emily G; Seelaar, Harro ...

Subjects: Pathology; SEGMENTATION; Medizin

• Source: NeuroImage: Clinical, 30:102646. Elsevier BVNeuroImage: Clinical, 30:102646. ElsevierBocchetta, M, Todd, E G, Peakman, G, Cash, D M, Convery, R S, Russell, L L, Thomas, D L, Iglesias, J E,

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Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort.

• Authors : Samra, Kiran; MacDougall, Amy M; Moreno, Fermin ...

Subjects: info:eu-repo/classification/ddc/610; Humans; Frontotemporal Dementia: diagnostic imagingDE

• Source: Journal of the neurological sciences 451, 120711 (2023). doi:10.1016/j.jns.2023.120711

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A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers

• Authors : Yolande A.L. Pijnenburg; Alessandro Padovani; Lieke H.H. Meeter ...

Subjects: medicine.medical_specialty; Neurology; NEFM

• Source: MOLECULAR NEURODEGENERATION, 16(1):79. BioMed CentralMolecular NeurodegenerationMolecular Neurodegeneration, Vol 16, Iss 1, Pp 1-14 (2021)Molecular Neurodegeneration, 16(1):79.

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