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Human Molecular Genetics|May 13, 2005
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau regionMarc Cruts, Rosa Rademakers, Ilse Gijselinck, et al.Journal of the American Geriatrics Society|December 2, 2004
Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's diseaseTischa J M van der Cammen, Esther A Croes, Bart Dermaut, et al.Journal of Neuropathology and Experimental Neurology|May 3, 2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration familyDaniel Pirici, Rik Vandenberghe, Rosa Rademakers, et al.American Journal of Human Genetics|May 7, 2002
The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sampleBart Dermaut, Jessie Theuns, Kristel Sleegers, et al.Cell Reports|January 22, 2013
TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in DrosophilaLies Vanden Broeck, Marina Naval-Sánchez, Yoshitsugu Adachi, et al.Neurobiology of Aging|January 10, 2006
Dose dependent effect of APOE epsilon4 on behavioral symptoms in frontal lobe dementiaSebastiaan Engelborghs, Bart Dermaut, Peter Mariën, et al.European Journal of Human Genetics : EJHG|February 19, 2004
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob diseaseEsther A Croes, Behrooz Z Alizadeh, Aida M Bertoli-Avella, et al.Neurology|January 21, 2018
Teenage-onset progressive myoclonic epilepsy due to a familial <i>C9orf72</i> repeat expansionJelle van den Ameele, Ivana Jedlickova, Anna Pristoupilova, et al.Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.Neurobiology of Disease|June 12, 2021
Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosisJulie van der Zee, Lubina Dillen, Yalda Baradaran-Heravi, et al.Pageof 6