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P De Deyn

Showing results (431-440 of 493) with videos related to

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Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Human Molecular Genetics|June 13, 1998
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsE Fransen, R D'Hooge, G Van Camp, et al.
Brain : a Journal of Neurology|February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Neurology|August 26, 2009
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159HisJ van der Zee, D Pirici, T Van Langenhove, et al.
Alzheimer Disease and Associated Disorders|December 1, 2017
Assessing Fitness to Drive in Patients With Different Types of DementiaDafne Piersma, Anselm B M Fuermaier, Dick De Waard, et al.
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.
Molecular Neurodegeneration|January 18, 2012
Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer riskKarolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, 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.
Cerebral Circulation - Cognition and Behavior|January 4, 2024
Small vessel disease burden and functional brain connectivity in mild cognitive impairmentSofia Marcolini, Jaime D Mondragón, Esther E Bron, et al.
Neurology|April 3, 2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutationTobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, et al.
Pageof 50

Showing results (431-440 of 493) with videos related to

Sort By:
Pageof 50
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Human Molecular Genetics|June 13, 1998
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsE Fransen, R D'Hooge, G Van Camp, et al.
Brain : a Journal of Neurology|February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Neurology|August 26, 2009
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159HisJ van der Zee, D Pirici, T Van Langenhove, et al.
Alzheimer Disease and Associated Disorders|December 1, 2017
Assessing Fitness to Drive in Patients With Different Types of DementiaDafne Piersma, Anselm B M Fuermaier, Dick De Waard, et al.
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.
Molecular Neurodegeneration|January 18, 2012
Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer riskKarolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, 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.
Cerebral Circulation - Cognition and Behavior|January 4, 2024
Small vessel disease burden and functional brain connectivity in mild cognitive impairmentSofia Marcolini, Jaime D Mondragón, Esther E Bron, et al.
Neurology|April 3, 2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutationTobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, et al.
Pageof 50