Showing results (61-70 of 102) with videos related to
Sort By:
Pageof 11
Neurobiology of Aging|October 15, 2013
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementiaElise Cuyvers, Karolien Bettens, Stéphanie Philtjens, et al.Neurobiology of Aging|January 11, 2017
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patientsFederica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, et al.Brain : a Journal of Neurology|September 29, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrumHelena Gossye, Sara Van Mossevelde, Anne Sieben, et al.Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.Nature|July 25, 2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Marc Cruts, Ilse Gijselinck, Julie van der Zee, et al.Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.Neurology|November 20, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohortIlse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.Alzheimer'S Research & Therapy|January 23, 2024
Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection methodAmber Nous, Laura Seynaeve, Odile Feys, et al.Pageof 11