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T Stojkovic

Showing results (111-120 of 121) with videos related to

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Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.
Revue Neurologique|December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.
Revue Neurologique|December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 13