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P Sindou

Showing results (41-50 of 51) with videos related to

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Acta Neurochirurgica|February 9, 2010
Percutaneous approach to the foramen ovale: an anatomical study of the extracranial trajectory with the incorrect trajectories to be avoidedJorge E Alvernia, Marc P Sindou, Nguyen D Dang, et al.
Acta Neuropathologica|July 10, 2004
Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic studyR De Armas, P Sindou, A Gelot, et al.
Acta Neuropathologica|September 14, 1999
Expression of myelin proteins in the adult heterozygous Trembler mouseJ M Vallat, P Sindou, B Garbay, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|May 8, 2004
Atypical electrophysiologic findings in chronic inflammatory demyelinating polyneuropathy (CIDP)--diagnosis confirmed by nerve biopsyS Boukhris, L Magy, R Kabore, et al.
Acta Neurochirurgica|February 14, 2017
The maxillary artery and its variants: an anatomical study with neurosurgical applicationsJorge E Alvernia, Joaquin Hidalgo, Marc P Sindou, et al.
Annals of Neurology|June 1, 1996
Ultrastructural PMP22 expression in inherited demyelinating neuropathiesJ M Vallat, P Sindou, P M Preux, et al.
Journal of the Neurological Sciences|April 30, 1998
Serum autoantibodies to neurofilament proteins in sporadic amyotrophic lateral sclerosisP Couratier, F H Yi, J L Preud'homme, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
Muscle & Nerve|January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B diseaseP Sindou, J M Vallat, F Chapon, et al.
Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Acta Neurochirurgica|February 9, 2010
Percutaneous approach to the foramen ovale: an anatomical study of the extracranial trajectory with the incorrect trajectories to be avoidedJorge E Alvernia, Marc P Sindou, Nguyen D Dang, et al.
Acta Neuropathologica|July 10, 2004
Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic studyR De Armas, P Sindou, A Gelot, et al.
Acta Neuropathologica|September 14, 1999
Expression of myelin proteins in the adult heterozygous Trembler mouseJ M Vallat, P Sindou, B Garbay, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|May 8, 2004
Atypical electrophysiologic findings in chronic inflammatory demyelinating polyneuropathy (CIDP)--diagnosis confirmed by nerve biopsyS Boukhris, L Magy, R Kabore, et al.
Acta Neurochirurgica|February 14, 2017
The maxillary artery and its variants: an anatomical study with neurosurgical applicationsJorge E Alvernia, Joaquin Hidalgo, Marc P Sindou, et al.
Annals of Neurology|June 1, 1996
Ultrastructural PMP22 expression in inherited demyelinating neuropathiesJ M Vallat, P Sindou, P M Preux, et al.
Journal of the Neurological Sciences|April 30, 1998
Serum autoantibodies to neurofilament proteins in sporadic amyotrophic lateral sclerosisP Couratier, F H Yi, J L Preud'homme, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
Muscle & Nerve|January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B diseaseP Sindou, J M Vallat, F Chapon, et al.
Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Pageof 6