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Wim Robberecht

Showing results (81-90 of 182) with videos related to

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Neuroscience Letters|July 6, 2004
Long-lasting changes in GABA responsiveness in cultured neuronsJoelle N Chabwine, Philip Van Damme, Jan Eggermont, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 21, 2017
Prognostic value of clinical and electrodiagnostic parameters at time of diagnosis in patients with amyotrophic lateral sclerosisWendeline Reniers, Maarten Schrooten, Kristl G Claeys, et al.
Journal of Neurochemistry|December 24, 2009
Pathogenic cysteine mutations affect progranulin function and production of mature granulinsJun Wang, Philip Van Damme, Carlos Cruchaga, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entityJonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Nature Medicine|July 26, 2011
HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth diseaseConstantin d'Ydewalle, Jyothsna Krishnan, Driss M Chiheb, et al.
Neurobiology of Disease|July 17, 2018
Astrocyte-derived Jagged-1 mitigates deleterious Notch signaling in amyotrophic lateral sclerosisAnnelies Nonneman, Nathan Criem, Sebastian A Lewandowski, et al.
Frontiers in Neuroscience|December 6, 2019
Lowering EphA4 Does Not Ameliorate Disease in a Mouse Model for Severe Spinal Muscular AtrophyLindsay Poppe, Silke Smolders, Laura Rué, et al.
Brain : a Journal of Neurology|February 5, 2013
Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosisThomas Philips, Andre Bento-Abreu, Annelies Nonneman, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
Report from the Italian Ministerial Committee regarding the diagnosis, care and assistance of patients with ALSCaterina Bendotti, Adriano Chiò, Maria Elena Congiu, et al.
Biochemical and Biophysical Research Communications|November 8, 2012
Neuronal overexpression of IP₃ receptor 2 is detrimental in mutant SOD1 miceKim A Staats, Elke Bogaert, Nicole Hersmus, et al.
Pageof 19

Showing results (81-90 of 182) with videos related to

Sort By:
Pageof 19
Neuroscience Letters|July 6, 2004
Long-lasting changes in GABA responsiveness in cultured neuronsJoelle N Chabwine, Philip Van Damme, Jan Eggermont, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 21, 2017
Prognostic value of clinical and electrodiagnostic parameters at time of diagnosis in patients with amyotrophic lateral sclerosisWendeline Reniers, Maarten Schrooten, Kristl G Claeys, et al.
Journal of Neurochemistry|December 24, 2009
Pathogenic cysteine mutations affect progranulin function and production of mature granulinsJun Wang, Philip Van Damme, Carlos Cruchaga, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entityJonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Nature Medicine|July 26, 2011
HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth diseaseConstantin d'Ydewalle, Jyothsna Krishnan, Driss M Chiheb, et al.
Neurobiology of Disease|July 17, 2018
Astrocyte-derived Jagged-1 mitigates deleterious Notch signaling in amyotrophic lateral sclerosisAnnelies Nonneman, Nathan Criem, Sebastian A Lewandowski, et al.
Frontiers in Neuroscience|December 6, 2019
Lowering EphA4 Does Not Ameliorate Disease in a Mouse Model for Severe Spinal Muscular AtrophyLindsay Poppe, Silke Smolders, Laura Rué, et al.
Brain : a Journal of Neurology|February 5, 2013
Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosisThomas Philips, Andre Bento-Abreu, Annelies Nonneman, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
Report from the Italian Ministerial Committee regarding the diagnosis, care and assistance of patients with ALSCaterina Bendotti, Adriano Chiò, Maria Elena Congiu, et al.
Biochemical and Biophysical Research Communications|November 8, 2012
Neuronal overexpression of IP₃ receptor 2 is detrimental in mutant SOD1 miceKim A Staats, Elke Bogaert, Nicole Hersmus, et al.
Pageof 19