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Vincent Timmerman

Showing results (81-90 of 152) with videos related to

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Journal of Neurology|March 15, 2014
Whole-exome sequencing in patients with inherited neuropathies: outcome and challengesMaria Schabhüttl, Thomas Wieland, Jan Senderek, et al.
Human Molecular Genetics|June 12, 2010
Mutant HSPB8 causes motor neuron-specific neurite degenerationJoy Irobi, Leonardo Almeida-Souza, Bob Asselbergh, et al.
Journal of Extracellular Vesicles|March 12, 2021
Microglial derived extracellular vesicles activate autophagy and mediate multi-target signaling to maintain cellular homeostasisBram Van den Broek, Isabel Pintelon, Ibrahim Hamad, et al.
Neuromuscular Disorders : NMD|December 24, 2005
Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IVNathalie Verpoorten, Kristl G Claeys, Liesbet Deprez, et al.
European Journal of Human Genetics : EJHG|September 25, 2025
A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathyLiedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, et al.
American Journal of Human Genetics|November 8, 2003
Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35Albena Jordanova, Florian P Thomas, Velina Guergueltcheva, et al.
American Journal of Human Genetics|May 14, 2013
Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritanceKristien Peeters, Ivan Litvinenko, Bob Asselbergh, et al.
Human Mutation|August 6, 2016
Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1Simona Capponi, Thomas Geuens, Alessandro Geroldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 30, 2009
Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathyErik Storkebaum, Ricardo Leitão-Gonçalves, Tanja Godenschwege, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 28, 2011
Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathyLeonardo Almeida-Souza, Bob Asselbergh, Constantin d'Ydewalle, et al.
Pageof 16

Showing results (81-90 of 152) with videos related to

Sort By:
Pageof 16
Journal of Neurology|March 15, 2014
Whole-exome sequencing in patients with inherited neuropathies: outcome and challengesMaria Schabhüttl, Thomas Wieland, Jan Senderek, et al.
Human Molecular Genetics|June 12, 2010
Mutant HSPB8 causes motor neuron-specific neurite degenerationJoy Irobi, Leonardo Almeida-Souza, Bob Asselbergh, et al.
Journal of Extracellular Vesicles|March 12, 2021
Microglial derived extracellular vesicles activate autophagy and mediate multi-target signaling to maintain cellular homeostasisBram Van den Broek, Isabel Pintelon, Ibrahim Hamad, et al.
Neuromuscular Disorders : NMD|December 24, 2005
Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IVNathalie Verpoorten, Kristl G Claeys, Liesbet Deprez, et al.
European Journal of Human Genetics : EJHG|September 25, 2025
A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathyLiedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, et al.
American Journal of Human Genetics|November 8, 2003
Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35Albena Jordanova, Florian P Thomas, Velina Guergueltcheva, et al.
American Journal of Human Genetics|May 14, 2013
Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritanceKristien Peeters, Ivan Litvinenko, Bob Asselbergh, et al.
Human Mutation|August 6, 2016
Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1Simona Capponi, Thomas Geuens, Alessandro Geroldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 30, 2009
Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathyErik Storkebaum, Ricardo Leitão-Gonçalves, Tanja Godenschwege, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 28, 2011
Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathyLeonardo Almeida-Souza, Bob Asselbergh, Constantin d'Ydewalle, et al.
Pageof 16