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Marc Cruts

Showing results (51-60 of 85) with videos related to

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American Journal of Human Genetics|September 22, 2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sampleRosa Rademakers, Marc Cruts, Kristel Sleegers, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 4, 2011
Rescue of progranulin deficiency associated with frontotemporal lobar degeneration by alkalizing reagents and inhibition of vacuolar ATPaseAnja Capell, Sabine Liebscher, Katrin Fellerer, et al.
Annals of Neurology|May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurobiology of Aging|January 29, 2013
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairmentRita Cacace, Caroline Van Cauwenberghe, Karolien Bettens, et al.
Brain : a Journal of Neurology|March 1, 2011
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortJulie van der Zee, Tim Van Langenhove, Gernot Kleinberger, 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.
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.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2013
Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowthBettina Schmid, Alexander Hruscha, Sebastian Hogl, 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.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|September 22, 2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sampleRosa Rademakers, Marc Cruts, Kristel Sleegers, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 4, 2011
Rescue of progranulin deficiency associated with frontotemporal lobar degeneration by alkalizing reagents and inhibition of vacuolar ATPaseAnja Capell, Sabine Liebscher, Katrin Fellerer, et al.
Annals of Neurology|May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurobiology of Aging|January 29, 2013
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairmentRita Cacace, Caroline Van Cauwenberghe, Karolien Bettens, et al.
Brain : a Journal of Neurology|March 1, 2011
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortJulie van der Zee, Tim Van Langenhove, Gernot Kleinberger, 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.
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.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2013
Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowthBettina Schmid, Alexander Hruscha, Sebastian Hogl, 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.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Pageof 9