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T Stojkovic

Showing results (81-90 of 121) with videos related to

Pageof 13
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Revue Neurologique|April 9, 2002
[Treatment of progressive multiple sclerosis with cyclophosphamide]H Zephir, J De Seze, O Sénéchal, et al.
Revue Neurologique|April 23, 2004
[Neuromeningeal tuberculosis: the contribution of genetic amplification to diagnosis]J de Seze, L Deligne, L Defebvre, et al.
Revue Neurologique|December 19, 2000
[Clinical manifestations and therapeutic approach in neurosarcoidosis]D Ferriby, J de Seze, T Stojkovic, et al.
Neurology|February 10, 2010
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutationK G Claeys, T Maisonobe, J Böhm, et al.
Journal of the Neurological Sciences|February 10, 2006
Unusual ocular motor findings in multiple sclerosisJ de Seze, S Vukusic, M Viallet-Marcel, et al.
European Journal of Neurology|April 5, 2005
Brain MRI in late-onset multiple sclerosisJ de Seze, S Delalande, E Michelin, et al.
Revue Neurologique|December 24, 2022
Strategy for genetic analysis in hereditary neuropathyM Masingue, G Fernández-Eulate, R Debs, et al.
Neuromuscular Disorders : NMD|November 18, 2011
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutationsI Wargon, P Richard, T Kuntzer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 23, 2008
Relapsing demyelinating disease affecting both the central and peripheral nervous systemsH Zéphir, T Stojkovic, P Latour, et al.
Revue Neurologique|March 5, 2013
[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]B Eymard, T Stojkovic, D Sternberg, et al.
Pageof 13

Showing results (81-90 of 121) with videos related to

Sort By:
Pageof 13
Revue Neurologique|April 9, 2002
[Treatment of progressive multiple sclerosis with cyclophosphamide]H Zephir, J De Seze, O Sénéchal, et al.
Revue Neurologique|April 23, 2004
[Neuromeningeal tuberculosis: the contribution of genetic amplification to diagnosis]J de Seze, L Deligne, L Defebvre, et al.
Revue Neurologique|December 19, 2000
[Clinical manifestations and therapeutic approach in neurosarcoidosis]D Ferriby, J de Seze, T Stojkovic, et al.
Neurology|February 10, 2010
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutationK G Claeys, T Maisonobe, J Böhm, et al.
Journal of the Neurological Sciences|February 10, 2006
Unusual ocular motor findings in multiple sclerosisJ de Seze, S Vukusic, M Viallet-Marcel, et al.
European Journal of Neurology|April 5, 2005
Brain MRI in late-onset multiple sclerosisJ de Seze, S Delalande, E Michelin, et al.
Revue Neurologique|December 24, 2022
Strategy for genetic analysis in hereditary neuropathyM Masingue, G Fernández-Eulate, R Debs, et al.
Neuromuscular Disorders : NMD|November 18, 2011
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutationsI Wargon, P Richard, T Kuntzer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 23, 2008
Relapsing demyelinating disease affecting both the central and peripheral nervous systemsH Zéphir, T Stojkovic, P Latour, et al.
Revue Neurologique|March 5, 2013
[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]B Eymard, T Stojkovic, D Sternberg, et al.
Pageof 13