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J Pouget

Showing results (191-200 of 227) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
Journal of Medical Genetics|March 21, 1998
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2pO Heinzlef, C Paternotte, F Mahieux, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 19, 2004
A longitudinal study of the evolution of cognitive function and affective state in patients with amyotrophic lateral sclerosisM Kilani, J Micallef, C Soubrouillard, et al.
Revue Neurologique|May 26, 1999
[Superficial siderosis of the central nervous system]A Durieux, F Flocard, A Ferreira, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 21, 2009
Motor evoked potentials in clinically isolated syndrome suggestive of multiple sclerosisA Rico, B Audoin, J Franques, et al.
La Revue De Medecine Interne|October 5, 2010
[Bilateral xerophthalmia in a 60-year-old man]P Bélénotti, A Benyamine, H Bensahla, et al.
Neuropathology and Applied Neurobiology|November 26, 2003
Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM)M Civatte, N Schleinitz, P Krammer, et al.
Journal of Viral Hepatitis|November 1, 1996
Myasthenia gravis and hepatitis C virus infectionP Halfon, M Levy, M San Marco, et al.
Journal of Clinical Immunology|August 12, 2000
Humoral immunity against glutamic acid decarboxylase and tyrosine phosphatase IA-2 in Lambert-Eaton myasthenic syndromeL Hermitte, N Martin-Moutot, J Boucraut, et al.
Neurology|May 24, 2006
Diagnostic evaluation of clinically normal subjects with chronic hyperCKemiaC Fernandez, A Maues de Paula, D Figarella-Branger, et al.
Pageof 23

Showing results (191-200 of 227) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
Journal of Medical Genetics|March 21, 1998
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2pO Heinzlef, C Paternotte, F Mahieux, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 19, 2004
A longitudinal study of the evolution of cognitive function and affective state in patients with amyotrophic lateral sclerosisM Kilani, J Micallef, C Soubrouillard, et al.
Revue Neurologique|May 26, 1999
[Superficial siderosis of the central nervous system]A Durieux, F Flocard, A Ferreira, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 21, 2009
Motor evoked potentials in clinically isolated syndrome suggestive of multiple sclerosisA Rico, B Audoin, J Franques, et al.
La Revue De Medecine Interne|October 5, 2010
[Bilateral xerophthalmia in a 60-year-old man]P Bélénotti, A Benyamine, H Bensahla, et al.
Neuropathology and Applied Neurobiology|November 26, 2003
Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM)M Civatte, N Schleinitz, P Krammer, et al.
Journal of Viral Hepatitis|November 1, 1996
Myasthenia gravis and hepatitis C virus infectionP Halfon, M Levy, M San Marco, et al.
Journal of Clinical Immunology|August 12, 2000
Humoral immunity against glutamic acid decarboxylase and tyrosine phosphatase IA-2 in Lambert-Eaton myasthenic syndromeL Hermitte, N Martin-Moutot, J Boucraut, et al.
Neurology|May 24, 2006
Diagnostic evaluation of clinically normal subjects with chronic hyperCKemiaC Fernandez, A Maues de Paula, D Figarella-Branger, et al.
Pageof 23