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Cyril Goizet

Showing results (1-10 of 173) with videos related to

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Progress in Neurobiology|April 8, 2014
Zebrafish models of human motor neuron diseases: advantages and limitationsPatrick J Babin, Cyril Goizet, Demetrio Raldúa
Current Opinion in Neurology|July 14, 2020
MRI of neurodegeneration with brain iron accumulationStéphane Lehéricy, Emmanuel Roze, Cyril Goizet, et al.
Journal of the Neurological Sciences|March 15, 2019
Genetics of amyotrophic lateral sclerosis: A reviewStéphane Mathis, Cyril Goizet, Antoine Soulages, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 14, 2010
Ophthalmological features associated with COL4A1 mutationsIsabelle Coupry, Igor Sibon, Bruno Mortemousque, et al.
Journal of Huntington'S Disease|May 24, 2024
Intensification of Diurnal Abnormal Movements During Sleep in Huntington's DiseaseLouis Salaun, Thomas Bonduelle, Imad Ghorayeb, et al.
Neurology|February 13, 2018
Updating the classification of inherited neuropathies: Results of an international surveyLaurent Magy, Stéphane Mathis, Gwendal Le Masson, et al.
European Journal of Human Genetics : EJHG|January 15, 2004
Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophyCyril Goizet, Isabelle Coupry, Caroline Rooryck, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Severe Charcot-Marie-Tooth disease type 1E caused by a novel p.Phe84Leufs*24 PMP22 point mutationAnne Vital, Guilhem Sole, Philippe Casenave, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
BMC Neurology|February 13, 2022
Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxiaChristelle M Durand, Chloé Angelini, Vincent Michaud, et al.
Pageof 18

Showing results (1-10 of 173) with videos related to

Sort By:
Pageof 18
Progress in Neurobiology|April 8, 2014
Zebrafish models of human motor neuron diseases: advantages and limitationsPatrick J Babin, Cyril Goizet, Demetrio Raldúa
Current Opinion in Neurology|July 14, 2020
MRI of neurodegeneration with brain iron accumulationStéphane Lehéricy, Emmanuel Roze, Cyril Goizet, et al.
Journal of the Neurological Sciences|March 15, 2019
Genetics of amyotrophic lateral sclerosis: A reviewStéphane Mathis, Cyril Goizet, Antoine Soulages, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 14, 2010
Ophthalmological features associated with COL4A1 mutationsIsabelle Coupry, Igor Sibon, Bruno Mortemousque, et al.
Journal of Huntington'S Disease|May 24, 2024
Intensification of Diurnal Abnormal Movements During Sleep in Huntington's DiseaseLouis Salaun, Thomas Bonduelle, Imad Ghorayeb, et al.
Neurology|February 13, 2018
Updating the classification of inherited neuropathies: Results of an international surveyLaurent Magy, Stéphane Mathis, Gwendal Le Masson, et al.
European Journal of Human Genetics : EJHG|January 15, 2004
Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophyCyril Goizet, Isabelle Coupry, Caroline Rooryck, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Severe Charcot-Marie-Tooth disease type 1E caused by a novel p.Phe84Leufs*24 PMP22 point mutationAnne Vital, Guilhem Sole, Philippe Casenave, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
BMC Neurology|February 13, 2022
Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxiaChristelle M Durand, Chloé Angelini, Vincent Michaud, et al.
Pageof 18