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T Stojkovic

Showing results (21-30 of 121) with videos related to

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Revue Neurologique|March 6, 2003
[Hypertrophy of the biceps surae after post-radiation lumbar radiculopathy]T Stojkovic, J de Seze, J-F Hurtevent, et al.
Revue Neurologique|March 12, 2002
[Tubular aggregate congenital myopathy associated with neuromuscular block]H Zephir, T Stojkovic, C A Maurage, et al.
Revue Neurologique|April 27, 2002
[Chronic polyradiculoneuritis disclosing sarcoidosis]D Ferriby, T Stojkovic, J De Seze, et al.
Revue Neurologique|April 27, 2002
[Primary progressive forms of multiple sclerosis: application of the new diagnostic criteria in French]J De Seze, A Mackowiak, T Stojkovic, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 30, 2003
Is Devic's neuromyelitis optica a separate disease? A comparative study with multiple sclerosisJ de Seze, C Lebrun, T Stojkovic, et al.
Revue Neurologique|December 19, 2002
[Bilateral phrenic nerve paralysis, dysautonomia and restrictive cardiomyopathy in a case of POEMS syndrome]S Delalande, T Stojkovic, C Rose, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 9, 2004
Intravenous corticosteroids in the postpartum period for reduction of acute exacerbations in multiple sclerosisJ de Seze, M Chapelotte, S Delalande, et al.
Revue Neurologique|September 19, 2000
[Adenovirus myelitis and Epstein-Barr myelitis: two unusual viral causes with similar presentations]G Breteau, T Stojkovic, J De Seze, et al.
Revue Neurologique|April 2, 2002
[Hearing loss in multiple sclerosis: clinical, electrophysiologic and radiological study]J de Seze, R Assouad, T Stojkovic, et al.
Neuromuscular Disorders : NMD|June 16, 2005
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsiesH Zéphir, T Stojkovic, P Latour, et al.
Pageof 13

Showing results (21-30 of 121) with videos related to

Sort By:
Pageof 13
Revue Neurologique|March 6, 2003
[Hypertrophy of the biceps surae after post-radiation lumbar radiculopathy]T Stojkovic, J de Seze, J-F Hurtevent, et al.
Revue Neurologique|March 12, 2002
[Tubular aggregate congenital myopathy associated with neuromuscular block]H Zephir, T Stojkovic, C A Maurage, et al.
Revue Neurologique|April 27, 2002
[Chronic polyradiculoneuritis disclosing sarcoidosis]D Ferriby, T Stojkovic, J De Seze, et al.
Revue Neurologique|April 27, 2002
[Primary progressive forms of multiple sclerosis: application of the new diagnostic criteria in French]J De Seze, A Mackowiak, T Stojkovic, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 30, 2003
Is Devic's neuromyelitis optica a separate disease? A comparative study with multiple sclerosisJ de Seze, C Lebrun, T Stojkovic, et al.
Revue Neurologique|December 19, 2002
[Bilateral phrenic nerve paralysis, dysautonomia and restrictive cardiomyopathy in a case of POEMS syndrome]S Delalande, T Stojkovic, C Rose, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 9, 2004
Intravenous corticosteroids in the postpartum period for reduction of acute exacerbations in multiple sclerosisJ de Seze, M Chapelotte, S Delalande, et al.
Revue Neurologique|September 19, 2000
[Adenovirus myelitis and Epstein-Barr myelitis: two unusual viral causes with similar presentations]G Breteau, T Stojkovic, J De Seze, et al.
Revue Neurologique|April 2, 2002
[Hearing loss in multiple sclerosis: clinical, electrophysiologic and radiological study]J de Seze, R Assouad, T Stojkovic, et al.
Neuromuscular Disorders : NMD|June 16, 2005
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsiesH Zéphir, T Stojkovic, P Latour, et al.
Pageof 13