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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.Human Mutation|May 1, 2009
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian populationKaren Nuytemans, Bram Meeus, David Crosiers, et al.Journal of Applied Research in Intellectual Disabilities : JARID|July 2, 2021
Dementia in people with severe or profound intellectual (and multiple) disabilities: Focus group research into relevance, symptoms and training needsAlain D Dekker, Maureen B G Wissing, Aurora M Ulgiati, et al.Neurobiology of Aging|September 22, 2021
Neurogranin as biomarker in CSF is non-specific to Alzheimer's disease dementiaEline A J Willemse, Anne Sieben, Charisse Somers, et al.Human Molecular Genetics|March 19, 2004
Severely altered guanidino compound levels, disturbed body weight homeostasis and impaired fertility in a mouse model of guanidinoacetate N-methyltransferase (GAMT) deficiencyAndreas Schmidt, Bart Marescau, Ernest A Boehm, et al.Journal of Alzheimer'S Disease : JAD|June 25, 2023
Activation of TNF Receptor 2 Improves Synaptic Plasticity and Enhances Amyloid-β Clearance in an Alzheimer's Disease Mouse Model with Humanized TNF Receptor 2Natalia Ortí-Casañ, Harald Wajant, H Bea Kuiperij, et al.Neurobiology of Aging|November 1, 2011
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohortsTim Van Langenhove, Julie van der Zee, Sebastiaan Engelborghs, et al.Neurobiology of Aging|January 6, 2026
Rare ABCA7 mutations in Alzheimer's disease and cerebral amyloid angiopathy pathologyElisabeth Hendrickx Van de Craen, Liene Bossaerts, Anne Sieben, et al.Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 22, 2018
Monoaminergic impairment in Down syndrome with Alzheimer's disease compared to early-onset Alzheimer's diseaseAlain D Dekker, Yannick Vermeiren, Maria Carmona-Iragui, et al.The American Journal of Clinical Nutrition|June 26, 2002
Overexpression of arginase I in enterocytes of transgenic mice elicits a selective arginine deficiency and affects skin, muscle, and lymphoid developmentWouter J de Jonge, Marcella M Hallemeesch, Karin L Kwikkers, et al.Pageof 28