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P Corcia

Showing results (71-80 of 102) with videos related to

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Revue Neurologique|March 31, 2005
[Cyclosporin-induced toxic neuromyopathy]A-M Guennoc, P Corcia, A Al-Najjar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Respiratory onset in an ALS family with L144F SOD1 mutationP Corcia, P Petiot, Z Stevic, et al.
Journal of the Neurological Sciences|September 6, 2017
Low IDL-B and high LDL-1 subfraction levels in serum of ALS patientsJ B Delaye, F Patin, E Piver, et al.
Journal of the Neurological Sciences|August 20, 2011
Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucomaP Corcia, J Praline, A M Guennoc, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Revue Neurologique|November 14, 2025
Markers of presymptomatic amyotrophic lateral sclerosis: State of the art, practical implications and perspectivesM-H Soriani, H Blasco, P Corcia, et al.
Presse Medicale (Paris, France : 1983)|March 17, 2000
[Amyotrophic lateral sclerosis manifesting as cognitive disorders. Value of brain perfusion scintigraphic tomography in intensive care]E Hazouard, A M Bergemer-Fouquet, C Hommet, et al.
European Journal of Neurology|March 22, 2017
SOD1 mutation can mask C9orf72 abnormal expansionP Corcia, H Blasco, G Besson, et al.
Molecular Neurobiology|November 8, 2013
Advances in cellular models to explore the pathophysiology of amyotrophic lateral sclerosisC Veyrat-Durebex, P Corcia, A Dangoumau, et al.
Neurology|August 26, 2006
SMN1 gene, but not SMN2, is a risk factor for sporadic ALSP Corcia, W Camu, J-M Halimi, et al.
Pageof 11

Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
Revue Neurologique|March 31, 2005
[Cyclosporin-induced toxic neuromyopathy]A-M Guennoc, P Corcia, A Al-Najjar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Respiratory onset in an ALS family with L144F SOD1 mutationP Corcia, P Petiot, Z Stevic, et al.
Journal of the Neurological Sciences|September 6, 2017
Low IDL-B and high LDL-1 subfraction levels in serum of ALS patientsJ B Delaye, F Patin, E Piver, et al.
Journal of the Neurological Sciences|August 20, 2011
Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucomaP Corcia, J Praline, A M Guennoc, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Revue Neurologique|November 14, 2025
Markers of presymptomatic amyotrophic lateral sclerosis: State of the art, practical implications and perspectivesM-H Soriani, H Blasco, P Corcia, et al.
Presse Medicale (Paris, France : 1983)|March 17, 2000
[Amyotrophic lateral sclerosis manifesting as cognitive disorders. Value of brain perfusion scintigraphic tomography in intensive care]E Hazouard, A M Bergemer-Fouquet, C Hommet, et al.
European Journal of Neurology|March 22, 2017
SOD1 mutation can mask C9orf72 abnormal expansionP Corcia, H Blasco, G Besson, et al.
Molecular Neurobiology|November 8, 2013
Advances in cellular models to explore the pathophysiology of amyotrophic lateral sclerosisC Veyrat-Durebex, P Corcia, A Dangoumau, et al.
Neurology|August 26, 2006
SMN1 gene, but not SMN2, is a risk factor for sporadic ALSP Corcia, W Camu, J-M Halimi, et al.
Pageof 11