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Wim Robberecht

Showing results (121-130 of 182) with videos related to

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Scientific Reports|February 13, 2016
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTDSteven Boeynaems, Elke Bogaert, Emiel Michiels, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 25, 2016
C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosisJames Rooney, Isabella Fogh, Henk-Jan Westeneng, et al.
The Lancet. Neurology|February 1, 2017
Safety and efficacy of ozanezumab in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled, phase 2 trialVincent Meininger, Angela Genge, Leonard H van den Berg, et al.
Journal of the Peripheral Nervous System : JPNS|January 24, 2019
Efficacy and safety of IVIG in CIDP: Combined data of the PRIMA and PATH studiesIngemar S J Merkies, Ivo N van Schaik, Jean-Marc Léger, et al.
Protein Engineering, Design & Selection : PEDS|May 14, 2020
Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4VFilip Claes, Stanislav Rudyak, Angela S Laird, et al.
Nature Neuroscience|November 30, 2004
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALSErik Storkebaum, Diether Lambrechts, Mieke Dewerchin, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
Human Molecular Genetics|February 8, 2018
Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationAndre Bento-Abreu, Gunilla Jager, Bart Swinnen, et al.
Archives of Neurology|April 15, 2009
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromesFrans Brugman, Jan H Veldink, Hessel Franssen, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Pageof 19

Showing results (121-130 of 182) with videos related to

Sort By:
Pageof 19
Scientific Reports|February 13, 2016
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTDSteven Boeynaems, Elke Bogaert, Emiel Michiels, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 25, 2016
C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosisJames Rooney, Isabella Fogh, Henk-Jan Westeneng, et al.
The Lancet. Neurology|February 1, 2017
Safety and efficacy of ozanezumab in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled, phase 2 trialVincent Meininger, Angela Genge, Leonard H van den Berg, et al.
Journal of the Peripheral Nervous System : JPNS|January 24, 2019
Efficacy and safety of IVIG in CIDP: Combined data of the PRIMA and PATH studiesIngemar S J Merkies, Ivo N van Schaik, Jean-Marc Léger, et al.
Protein Engineering, Design & Selection : PEDS|May 14, 2020
Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4VFilip Claes, Stanislav Rudyak, Angela S Laird, et al.
Nature Neuroscience|November 30, 2004
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALSErik Storkebaum, Diether Lambrechts, Mieke Dewerchin, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
Human Molecular Genetics|February 8, 2018
Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationAndre Bento-Abreu, Gunilla Jager, Bart Swinnen, et al.
Archives of Neurology|April 15, 2009
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromesFrans Brugman, Jan H Veldink, Hessel Franssen, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Pageof 19