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Cyril Goizet

Showing results (51-60 of 173) with videos related to

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European Journal of Medical Genetics|August 25, 2018
Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variantChloé Angelini, Julien Van Gils, Antoine Bigourdan, et al.
Neuropediatrics|March 7, 2020
Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIAChloé Angelini, Marie Thibaud, Nathalie Aladjidi, et al.
European Neurology|August 22, 2012
Clinical and radiological characteristics in multiple sclerosis patients with large cavitary lesionsDimitri Renard, Bruno Brochet, Sandra Vukusic, et al.
CNS Neuroscience & Therapeutics|June 15, 2016
Pain in Fabry Disease: Practical Recommendations for Diagnosis and TreatmentJuan M Politei, Didier Bouhassira, Dominique P Germain, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 22, 2017
Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin α<sub>IIb</sub>β<sub>3</sub> ActivationEliane Berrou, Frédéric Adam, Marilyne Lebret, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 23, 2021
SOD1-related ALS with anticipation in a large family from MartiniqueAnna-Gaelle Giguet-Valard, Rémi Bellance, Séverine Jeannin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2009
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)Fabienne Ory-Magne, Christine Brefel-Courbon, Pierre Payoux, et al.
European Journal of Medical Genetics|February 28, 2012
Atypical male and female presentations of FLNA-related periventricular nodular heterotopiaPatricia Fergelot, Isabelle Coupry, Caroline Rooryck, et al.
Rheumatology (Oxford, England)|March 25, 2017
Neutrophil-derived mitochondrial DNA promotes receptor activator of nuclear factor κB and its ligand signalling in rheumatoid arthritisAnne Contis, Stéphane Mitrovic, Julie Lavie, et al.
Human Molecular Genetics|December 24, 2016
Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylationJulie Lavie, Román Serrat, Nadège Bellance, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
European Journal of Medical Genetics|August 25, 2018
Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variantChloé Angelini, Julien Van Gils, Antoine Bigourdan, et al.
Neuropediatrics|March 7, 2020
Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIAChloé Angelini, Marie Thibaud, Nathalie Aladjidi, et al.
European Neurology|August 22, 2012
Clinical and radiological characteristics in multiple sclerosis patients with large cavitary lesionsDimitri Renard, Bruno Brochet, Sandra Vukusic, et al.
CNS Neuroscience & Therapeutics|June 15, 2016
Pain in Fabry Disease: Practical Recommendations for Diagnosis and TreatmentJuan M Politei, Didier Bouhassira, Dominique P Germain, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 22, 2017
Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin α<sub>IIb</sub>β<sub>3</sub> ActivationEliane Berrou, Frédéric Adam, Marilyne Lebret, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 23, 2021
SOD1-related ALS with anticipation in a large family from MartiniqueAnna-Gaelle Giguet-Valard, Rémi Bellance, Séverine Jeannin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2009
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)Fabienne Ory-Magne, Christine Brefel-Courbon, Pierre Payoux, et al.
European Journal of Medical Genetics|February 28, 2012
Atypical male and female presentations of FLNA-related periventricular nodular heterotopiaPatricia Fergelot, Isabelle Coupry, Caroline Rooryck, et al.
Rheumatology (Oxford, England)|March 25, 2017
Neutrophil-derived mitochondrial DNA promotes receptor activator of nuclear factor κB and its ligand signalling in rheumatoid arthritisAnne Contis, Stéphane Mitrovic, Julie Lavie, et al.
Human Molecular Genetics|December 24, 2016
Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylationJulie Lavie, Román Serrat, Nadège Bellance, et al.
Pageof 18