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Emmanuel Fournier

Showing results (51-60 of 57) with videos related to

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Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Plos One|July 27, 2018
Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA studyAurélie Chabanon, Andreea Mihaela Seferian, Aurore Daron, et al.
Annals of Clinical and Translational Neurology|April 25, 2015
Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patientsGaëlle Bruneteau, Stéphanie Bauché, Jose Luis Gonzalez de Aguilar, et al.
Brain and Behavior|November 10, 2022
Older patients with COVID-19 and neuropsychiatric conditions: A study of risk factors for mortalityVi-Huong Nguyen-Michel, Marion Houot, Cécile Delorme, et al.
Lancet (London, England)|March 8, 2016
Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control studyVan-Mai Cao-Lormeau, Alexandre Blake, Sandrine Mons, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
Journal of Neurology|July 17, 2017
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathyStéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Plos One|July 27, 2018
Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA studyAurélie Chabanon, Andreea Mihaela Seferian, Aurore Daron, et al.
Annals of Clinical and Translational Neurology|April 25, 2015
Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patientsGaëlle Bruneteau, Stéphanie Bauché, Jose Luis Gonzalez de Aguilar, et al.
Brain and Behavior|November 10, 2022
Older patients with COVID-19 and neuropsychiatric conditions: A study of risk factors for mortalityVi-Huong Nguyen-Michel, Marion Houot, Cécile Delorme, et al.
Lancet (London, England)|March 8, 2016
Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control studyVan-Mai Cao-Lormeau, Alexandre Blake, Sandrine Mons, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
Journal of Neurology|July 17, 2017
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathyStéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, et al.
Pageof 6