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J Pouget

Showing results (111-120 of 227) with videos related to

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Clinical Neuropharmacology|December 1, 1996
Adenosine and the nervous system: clinical implicationsR Guieu, F Couraud, J Pouget, et al.
Revue Neurologique|January 1, 1982
[Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders]G Serratrice, J Pouget, J F Pellissier, et al.
Acta Oto-Laryngologica|December 10, 1999
Quantitative voice analysis in the assessment of bulbar involvement in amyotrophic lateral sclerosisD Robert, J Pouget, A Giovanni, et al.
La Revue De Medecine Interne|December 24, 2013
[Necrotizing myopathies: From genetic to acquired forms]E Salort-Campana, A M De Paula, D Figarella-Branger, et al.
Journal of Neurology|December 20, 2005
Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variabilityW Casseron, J P Azulay, E Guedj, et al.
Revue Neurologique|January 1, 1983
[Quadriceps myopathy or amyotrophic quadriceps syndrome. Nosologic study apropos of 10 cases]G Serratrice, J L Gastaut, J F Pellissier, et al.
Revue Neurologique|January 1, 1982
[Scapuloperoneal syndromes]G Serratrice, J F Pellissier, J Pouget, et al.
Revue Neurologique|January 1, 1992
[Familial amyotrophic lateral sclerosis associated with Huntington chorea with increased aspartate level in the cerebrospinal fluid]O Blin, D Samuel, R Guieu, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1989
[Short-term double-blind vs placebo trial of L-threonine in amyotrophic lateral sclerosis]O Blin, G Serratrice, J Pouget, et al.
Advances in Neurology|January 1, 1995
Anti-calcium channel autoantibodies in amyotrophic lateral sclerosis. A review of the evidenceM J Seagar, N Martin-Moutot, C Leveque, et al.
Pageof 23

Showing results (111-120 of 227) with videos related to

Sort By:
Pageof 23
Clinical Neuropharmacology|December 1, 1996
Adenosine and the nervous system: clinical implicationsR Guieu, F Couraud, J Pouget, et al.
Revue Neurologique|January 1, 1982
[Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders]G Serratrice, J Pouget, J F Pellissier, et al.
Acta Oto-Laryngologica|December 10, 1999
Quantitative voice analysis in the assessment of bulbar involvement in amyotrophic lateral sclerosisD Robert, J Pouget, A Giovanni, et al.
La Revue De Medecine Interne|December 24, 2013
[Necrotizing myopathies: From genetic to acquired forms]E Salort-Campana, A M De Paula, D Figarella-Branger, et al.
Journal of Neurology|December 20, 2005
Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variabilityW Casseron, J P Azulay, E Guedj, et al.
Revue Neurologique|January 1, 1983
[Quadriceps myopathy or amyotrophic quadriceps syndrome. Nosologic study apropos of 10 cases]G Serratrice, J L Gastaut, J F Pellissier, et al.
Revue Neurologique|January 1, 1982
[Scapuloperoneal syndromes]G Serratrice, J F Pellissier, J Pouget, et al.
Revue Neurologique|January 1, 1992
[Familial amyotrophic lateral sclerosis associated with Huntington chorea with increased aspartate level in the cerebrospinal fluid]O Blin, D Samuel, R Guieu, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1989
[Short-term double-blind vs placebo trial of L-threonine in amyotrophic lateral sclerosis]O Blin, G Serratrice, J Pouget, et al.
Advances in Neurology|January 1, 1995
Anti-calcium channel autoantibodies in amyotrophic lateral sclerosis. A review of the evidenceM J Seagar, N Martin-Moutot, C Leveque, et al.
Pageof 23