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S Sacconi

Showing results (1-10 of 31) with videos related to

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Revue Neurologique|August 24, 2013
[Facioscapulohumeral muscular dystrophy type 2]S Sacconi, C Desnuelle
Archives of Neurology|October 27, 2001
Acute disseminated encephalomyelitis associated with hepatitis C virus infectionS Sacconi, L Salviati, E Merelli
Revue Neurologique|November 13, 2010
[Retinal involvement and genetic myopathy]S Sacconi, S Baillif-Gostoli, C Desnuelle
Revue Neurologique|June 16, 2009
[Validity of the motor function measurement scale when routinely used in the follow-up of adult outpatients in a neuromuscular center]C Benaïm, S Sacconi, M Fournier-Mehouas, et al.
Revue Neurologique|June 3, 2009
[Anti-MAG paraproteinemic demyelinating polyneuropathy: a clinical, biological, electrophysiological and anatomopathological descriptive study of a 13-patients' cohort]M Launay, E Delmont, C Benaim, et al.
Revue Neurologique|September 24, 2008
[McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients]E Delmont, S Sacconi, J-L Berge-Lefranc, et al.
Journal of Medical Genetics|July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patientsL Davidovic, S Sacconi, E G Bechara, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Neurology|June 9, 2019
Comparison of high-frequency and ultrahigh-frequency probes in chronic inflammatory demyelinating polyneuropathyAngela Puma, N Azulay, N Grecu, et al.
Neurology|October 25, 2006
Diagnostic challenges in facioscapulohumeral muscular dystrophyS Sacconi, L Salviati, I Bourget, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Revue Neurologique|August 24, 2013
[Facioscapulohumeral muscular dystrophy type 2]S Sacconi, C Desnuelle
Archives of Neurology|October 27, 2001
Acute disseminated encephalomyelitis associated with hepatitis C virus infectionS Sacconi, L Salviati, E Merelli
Revue Neurologique|November 13, 2010
[Retinal involvement and genetic myopathy]S Sacconi, S Baillif-Gostoli, C Desnuelle
Revue Neurologique|June 16, 2009
[Validity of the motor function measurement scale when routinely used in the follow-up of adult outpatients in a neuromuscular center]C Benaïm, S Sacconi, M Fournier-Mehouas, et al.
Revue Neurologique|June 3, 2009
[Anti-MAG paraproteinemic demyelinating polyneuropathy: a clinical, biological, electrophysiological and anatomopathological descriptive study of a 13-patients' cohort]M Launay, E Delmont, C Benaim, et al.
Revue Neurologique|September 24, 2008
[McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients]E Delmont, S Sacconi, J-L Berge-Lefranc, et al.
Journal of Medical Genetics|July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patientsL Davidovic, S Sacconi, E G Bechara, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Neurology|June 9, 2019
Comparison of high-frequency and ultrahigh-frequency probes in chronic inflammatory demyelinating polyneuropathyAngela Puma, N Azulay, N Grecu, et al.
Neurology|October 25, 2006
Diagnostic challenges in facioscapulohumeral muscular dystrophyS Sacconi, L Salviati, I Bourget, et al.
Pageof 4