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T Stojkovic

Showing results (101-110 of 121) with videos related to

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European Journal of Neurology|October 12, 2013
Antibodies to clustered acetylcholine receptor: expanding the phenotypeP Devic, P Petiot, T Simonet, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
Revue Neurologique|May 2, 2020
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases NetworkG Solé, E Salort-Campana, Y Pereon, et al.
European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Neurology|July 23, 2003
Alpha-fodrin autoantibodies in the differential diagnosis of MS and Sjögren syndromeJ de Seze, S Dubucquoi, A L Fauchais, et al.
Brain : a Journal of Neurology|July 19, 2001
Acute myelopathies: Clinical, laboratory and outcome profiles in 79 casesJ de Seze, T Stojkovic, G Breteau, et al.
Acta Oncologica (Stockholm, Sweden)|December 16, 2017
Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disabilityM J Ibañez-Juliá, G Berzero, G Reyes-Botero, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
European Journal of Neurology|August 7, 2020
Demyelinating Charcot-Marie-Tooth neuropathy associated with FBLN5 mutationsD Safka Brozkova, T Stojkovic, J Haberlová, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 13
European Journal of Neurology|October 12, 2013
Antibodies to clustered acetylcholine receptor: expanding the phenotypeP Devic, P Petiot, T Simonet, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
Revue Neurologique|May 2, 2020
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases NetworkG Solé, E Salort-Campana, Y Pereon, et al.
European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Neurology|July 23, 2003
Alpha-fodrin autoantibodies in the differential diagnosis of MS and Sjögren syndromeJ de Seze, S Dubucquoi, A L Fauchais, et al.
Brain : a Journal of Neurology|July 19, 2001
Acute myelopathies: Clinical, laboratory and outcome profiles in 79 casesJ de Seze, T Stojkovic, G Breteau, et al.
Acta Oncologica (Stockholm, Sweden)|December 16, 2017
Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disabilityM J Ibañez-Juliá, G Berzero, G Reyes-Botero, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
European Journal of Neurology|August 7, 2020
Demyelinating Charcot-Marie-Tooth neuropathy associated with FBLN5 mutationsD Safka Brozkova, T Stojkovic, J Haberlová, et al.
Pageof 13