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Anthony Behin

Showing results (41-50 of 92) with videos related to

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Arthritis and Rheumatism|March 15, 2011
Correlation of anti-signal recognition particle autoantibody levels with creatine kinase activity in patients with necrotizing myopathyOlivier Benveniste, Laurent Drouot, Fabienne Jouen, et al.
Molecular Genetics and Metabolism|September 11, 2017
Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIaValérie Decostre, Pascal Laforêt, Marie De Antonio, et al.
Journal of Neuromuscular Diseases|December 28, 2017
Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular DisordersAbdallah Fayssoil, Anthony Behin, Adam Ogna, et al.
European Journal of Neurology|September 12, 2022
Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisalAndreas Meisel, Fulvio Baggi, Anthony Behin, et al.
Neuro-Oncology|January 31, 2006
Phase 1 trial of a CpG oligodeoxynucleotide for patients with recurrent glioblastomaAlexandre Carpentier, Florence Laigle-Donadey, Sarah Zohar, et al.
Plos One|April 28, 2016
Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2DAbdallah Fayssoil, Adam Ogna, Cendrine Chaffaut, et al.
Genetic Testing and Molecular Biomarkers|June 21, 2018
Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French CohortAlzira Alves de Siqueira Carvalho, Emmanuele Lacene, Guy Brochier, et al.
Brain Communications|May 25, 2022
Unravelling the impact of frontal lobe impairment for social dysfunction in myotonic dystrophy type 1Alexandre Morin, Aurelie Funkiewiez, Alexandre Routier, et al.
Muscle & Nerve|March 4, 2017
Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencingMathieu Cerino, Svetlana Gorokhova, Pascal Laforet, et al.
Scientific Reports|August 28, 2023
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndromeMarion Masingue, Olivia Cattaneo, Nicolas Wolff, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
Arthritis and Rheumatism|March 15, 2011
Correlation of anti-signal recognition particle autoantibody levels with creatine kinase activity in patients with necrotizing myopathyOlivier Benveniste, Laurent Drouot, Fabienne Jouen, et al.
Molecular Genetics and Metabolism|September 11, 2017
Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIaValérie Decostre, Pascal Laforêt, Marie De Antonio, et al.
Journal of Neuromuscular Diseases|December 28, 2017
Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular DisordersAbdallah Fayssoil, Anthony Behin, Adam Ogna, et al.
European Journal of Neurology|September 12, 2022
Role of autoantibody levels as biomarkers in the management of patients with myasthenia gravis: A systematic review and expert appraisalAndreas Meisel, Fulvio Baggi, Anthony Behin, et al.
Neuro-Oncology|January 31, 2006
Phase 1 trial of a CpG oligodeoxynucleotide for patients with recurrent glioblastomaAlexandre Carpentier, Florence Laigle-Donadey, Sarah Zohar, et al.
Plos One|April 28, 2016
Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2DAbdallah Fayssoil, Adam Ogna, Cendrine Chaffaut, et al.
Genetic Testing and Molecular Biomarkers|June 21, 2018
Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French CohortAlzira Alves de Siqueira Carvalho, Emmanuele Lacene, Guy Brochier, et al.
Brain Communications|May 25, 2022
Unravelling the impact of frontal lobe impairment for social dysfunction in myotonic dystrophy type 1Alexandre Morin, Aurelie Funkiewiez, Alexandre Routier, et al.
Muscle & Nerve|March 4, 2017
Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencingMathieu Cerino, Svetlana Gorokhova, Pascal Laforet, et al.
Scientific Reports|August 28, 2023
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndromeMarion Masingue, Olivia Cattaneo, Nicolas Wolff, et al.
Pageof 10