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Julie van der Zee

Showing results (31-40 of 102) with videos related to

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Neurobiology of Aging|December 15, 2018
Presence of tau astrogliopathy in frontotemporal dementia caused by a novel Grn nonsense (Trp2*) mutationEstrella Gómez-Tortosa, Yalda Baradaran-Heravi, Valentina González Alvarez, et al.
Annals of Neurology|March 17, 2009
Serum biomarker for progranulin-associated frontotemporal lobar degenerationKristel Sleegers, Nathalie Brouwers, Philip Van Damme, et al.
Neurobiology of Aging|September 14, 2020
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriersCemile Koçoğlu, Helena Gossye, Lubina Dillen, et al.
Neurobiology of Aging|May 19, 2009
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationSara Rollinson, Jonathan D Rohrer, Julie van der Zee, et al.
Neurobiology of Aging|January 15, 2013
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patientsLubina Dillen, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Alzheimer'S Research & Therapy|September 12, 2020
Amyloid-β<sub>1-43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutationsFederica Perrone, Maria Bjerke, Elisabeth Hens, et al.
Alzheimer'S Research & Therapy|March 22, 2018
Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degenerationJoery Goossens, Maria Bjerke, Sara Van Mossevelde, 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.
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.
Pageof 11

Showing results (31-40 of 102) with videos related to

Sort By:
Pageof 11
Neurobiology of Aging|December 15, 2018
Presence of tau astrogliopathy in frontotemporal dementia caused by a novel Grn nonsense (Trp2*) mutationEstrella Gómez-Tortosa, Yalda Baradaran-Heravi, Valentina González Alvarez, et al.
Annals of Neurology|March 17, 2009
Serum biomarker for progranulin-associated frontotemporal lobar degenerationKristel Sleegers, Nathalie Brouwers, Philip Van Damme, et al.
Neurobiology of Aging|September 14, 2020
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriersCemile Koçoğlu, Helena Gossye, Lubina Dillen, et al.
Neurobiology of Aging|May 19, 2009
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationSara Rollinson, Jonathan D Rohrer, Julie van der Zee, et al.
Neurobiology of Aging|January 15, 2013
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patientsLubina Dillen, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Alzheimer'S Research & Therapy|September 12, 2020
Amyloid-β<sub>1-43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutationsFederica Perrone, Maria Bjerke, Elisabeth Hens, et al.
Alzheimer'S Research & Therapy|March 22, 2018
Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degenerationJoery Goossens, Maria Bjerke, Sara Van Mossevelde, 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.
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.
Pageof 11