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Wim Robberecht

Showing results (131-140 of 182) with videos related to

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Brain : a Journal of Neurology|March 3, 2011
Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging studyMaaike M van der Graaff, Caroline A Sage, Matthan W A Caan, et al.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature Medicine|August 28, 2012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humansAnnelies Van Hoecke, Lies Schoonaert, Robin Lemmens, et al.
Brain : a Journal of Neurology|March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation studyInes Dierick, Jonathan Baets, Joy Irobi, et al.
Nature Genetics|January 24, 2006
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyAlbena Jordanova, Joy Irobi, Florian P Thomas, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain Communications|October 28, 2021
<i>SCFD1</i> expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.
Neurobiology of Aging|April 23, 2010
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisElke Bogaert, An Goris, Philip Van Damme, et al.
Pageof 19

Showing results (131-140 of 182) with videos related to

Sort By:
Pageof 19
Brain : a Journal of Neurology|March 3, 2011
Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging studyMaaike M van der Graaff, Caroline A Sage, Matthan W A Caan, et al.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature Medicine|August 28, 2012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humansAnnelies Van Hoecke, Lies Schoonaert, Robin Lemmens, et al.
Brain : a Journal of Neurology|March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation studyInes Dierick, Jonathan Baets, Joy Irobi, et al.
Nature Genetics|January 24, 2006
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyAlbena Jordanova, Joy Irobi, Florian P Thomas, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain Communications|October 28, 2021
<i>SCFD1</i> expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.
Neurobiology of Aging|April 23, 2010
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisElke Bogaert, An Goris, Philip Van Damme, et al.
Pageof 19