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Julie van der Zee

Showing results (21-30 of 102) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 30, 2012
Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutationCatarina Chester, Mamede de Carvalho, Gabriel Miltenberger, et al.
Neurobiology of Aging|February 4, 2016
Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G₄C₂) repeat expansion in C9orf72 geneMaria Rosário Almeida, Liliana Letra, Paula Pires, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|August 4, 2015
Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementiaGabor G Kovacs, Julie van der Zee, Jakub Hort, et al.
Neurobiology of Aging|September 23, 2017
NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patientsHung Phuoc Nguyen, Sara Van Mossevelde, Lubina Dillen, et al.
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.
Neurobiology of Aging|June 4, 2018
Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosisFederica Perrone, Rita Cacace, Sara Van Mossevelde, et al.
Neurobiology of Aging|October 7, 2015
A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic functionEnriqueta Tristán-Clavijo, Rafael J Camacho-Garcia, Estefanía Robles-Lanuza, et al.
Acta Neuropathologica Communications|November 21, 2013
Promoter DNA methylation regulates progranulin expression and is altered in FTLDJulia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, et al.
EMBO Molecular Medicine|May 24, 2018
A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALSCarina Lehmer, Martin H Schludi, Linnea Ransom, et al.
Biomolecules|March 25, 2022
Frontotemporal Lobar Degeneration Case with an N-Terminal <i>TUBA4A</i> Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 PathologyEvelien Van Schoor, Mathieu Vandenbulcke, Valérie Bercier, et al.
Pageof 11

Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 30, 2012
Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutationCatarina Chester, Mamede de Carvalho, Gabriel Miltenberger, et al.
Neurobiology of Aging|February 4, 2016
Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G₄C₂) repeat expansion in C9orf72 geneMaria Rosário Almeida, Liliana Letra, Paula Pires, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|August 4, 2015
Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementiaGabor G Kovacs, Julie van der Zee, Jakub Hort, et al.
Neurobiology of Aging|September 23, 2017
NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patientsHung Phuoc Nguyen, Sara Van Mossevelde, Lubina Dillen, et al.
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.
Neurobiology of Aging|June 4, 2018
Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosisFederica Perrone, Rita Cacace, Sara Van Mossevelde, et al.
Neurobiology of Aging|October 7, 2015
A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic functionEnriqueta Tristán-Clavijo, Rafael J Camacho-Garcia, Estefanía Robles-Lanuza, et al.
Acta Neuropathologica Communications|November 21, 2013
Promoter DNA methylation regulates progranulin expression and is altered in FTLDJulia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, et al.
EMBO Molecular Medicine|May 24, 2018
A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALSCarina Lehmer, Martin H Schludi, Linnea Ransom, et al.
Biomolecules|March 25, 2022
Frontotemporal Lobar Degeneration Case with an N-Terminal <i>TUBA4A</i> Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 PathologyEvelien Van Schoor, Mathieu Vandenbulcke, Valérie Bercier, et al.
Pageof 11