Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI Study.

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Bibliographic Details
Title: Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI Study.
Authors: Russell LL; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom., Bouzigues A; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom., Convery RS; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom., Foster PH; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom., Ferry-Bolder E; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom., Cash DM; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom.; Centre for Medical Image Computing, University College London, United Kingdom., Van Swieten JC; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands., Jiskoot LC; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands., Seelaar H; Department of Neurology, Erasmus Medical Centre, Rotterdam, Netherlands., Moreno F; Cognitive Disorders Unit, Department of Neurology, Donostia University Hospital, San Sebastian, Gipuzkoa, Spain.; Neuroscience Area, Biodonostia Health Research Institute, San Sebastian, Gipuzkoa, Spain., Sánchez-Valle R; Alzheimer's disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacións Biomèdiques August Pi I Sunyer, University of Barcelona, Spain., Laforce R Jr; Département des Sciences Neurologiques, CHU de Québec, and Faculté de Médecine, Clinique Interdisciplinaire de Mémoire, Université Laval, Canada., Graff C; Center for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Bioclinicum, Karolinska Institutet, Solna, Sweden.; Unit for Hereditary Dementias, Theme Aging, Karolinska University Hospital, Solna, Sweden., Masellis M; Sunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Canada., Tartaglia MC; Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Canada., Rowe JB; Department of Clinical Neurosciences and Cambridge University Hospitals NHS Trust and Medical Research Council Cognition and Brain Sciences Unit, University of Cambridge, United Kingdom., Borroni B; Centre for Neurodegenerative Disorders, Department of Clinical and Experimental Sciences, University of Brescia, Italy., Finger E; Department of Clinical Neurological Sciences, University of Western Ontario, London, Canada., Synofzik M; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Germany.; Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany., Galimberti D; Department of Biomedical, Surgical and Dental Sciences, University of Milan, Italy.; Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy., Vandenberghe R; Laboratory for Cognitive Neurology, Department of Neurosciences, KU Leuven, Belgium.; Neurology Service, University Hospitals Leuven, Belgium.; Leuven Brain Institute, KU Leuven, Belgium., de Mendonça A; Faculty of Medicine, University of Lisbon, Portugal., Butler C; Nuffield Department of Clinical Neurosciences, Medical Sciences Division, University of Oxford, United Kingdom., Gerhard A; Division of Psychology Communication and Human Neuroscience Wolfson Molecular Imaging Centre, University of Manchester, United Kingdom.; Department of Nuclear Medicine, Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Germany.; Department of Geriatric Medicine, Klinikum Hochsauerland, Arnsberg, Germany., Ducharme S; Department of Psychiatry, Douglas Mental Health University Institute, McGill University, Montreal, Canada.; Department of Neurology and Neurosurgery, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, Canada., Le Ber I; Paris Brain Institute-Institut du Cerveau-ICM, Inserm U1127, CNRS UMR 7225, AP-HP-Hôpital Pitié-Salpêtrière (DMU Neurosciences Paris 6), Sorbonne Université, France.; Département de Neurologie, Centre de référence des démences rares ou précoces, IM2A, AP-HP-Hôpital Pitié-Salpêtrière (DMU Neurosciences Paris 6), Paris, France.; Département de Neurologie, AP-HP-Hôpital Pitié-Salpêtrière (DMU Neurosciences Paris 6), France., Santana I; Neurology Department, Centro Hospitalar e Universitário de Coimbra, Portugal.; Faculty of Medicine, University of Coimbra, Portugal.; Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, Portugal., Pasquier F; Univ Lille, France.; Inserm 1172, Lille, France.; CHU Lille, CNR-MAJ, Labex Distalz, LiCEND, France., Levin J; Neurologische Klinik und Poliklinik, Ludwig-Maximilians-Universität, Munich, Germany.; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Munich Cluster of Systems Neurology, Germany., Sorbi S; Department of Neurofarba, University of Florence, Italy.; IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy; and., Otto M; Department of Neurology, University of Ulm, German., Rohrer JD; Department of Neurodegenerative Disease, Dementia Research Centre, UCL Institute of Neurology, London, United Kingdom.
Corporate Authors: Genetic FTD Initiative (GENFI)
Source: Neurology. Genetics [Neurol Genet] 2025 Jul 21; Vol. 11 (4), pp. e200248. Date of Electronic Publication: 2025 Jul 21 (Print Publication: 2025).
Publication Type: Journal Article
Journal Info: Publisher: Published for the American Academy of Neurology by Wolters Kluwer Country of Publication: United States NLM ID: 101671068 Publication Model: eCollection Cited Medium: Print ISSN: 2376-7839 (Print) Linking ISSN: 23767839 NLM ISO Abbreviation: Neurol Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2376-7839
DOI:10.1212/NXG.0000000000200248