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E Plassart

Showing results (1-10 of 17) with videos related to

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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Genes with triplet repeats: a new class of mutations causing neurological diseasesE Plassart, B Fontaine
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|January 1, 1976
[Respiratory movements during sleep of the neonate at term: comparison of thoracic and abdominal recordings]L Curzi-Dascalova, E Plassart
Early Human Development|April 1, 1978
Respiratory and motor events in sleeping infants: their correlation with thoracico-abdominal respiratory relationshipsL Curzi-Dascalova, E Plassart
Brain Research. Brain Research Reviews|December 18, 2001
Neurosteroids: recent findingsE Plassart-Schiess, E E Baulieu
Molecular Aspects of Medicine|April 30, 1998
Diseases caused by voltage-gated ion channelsB Fontaine, E Plassart-Schiess, S Nicole
Annals of Clinical Biochemistry|February 17, 1998
Apolipoprotein E polymorphism in multiple sclerosisA Gervais, O Gaillard, E Plassart, et al.
The Journal of Physiology|May 23, 1998
Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell lineE Plassart-Schiess, L Lhuillier, A L George, et al.
Journal of the Neurological Sciences|August 14, 1998
Apolipoprotein E and multiple sclerosis: a biochemical and genetic investigationO Gaillard, A Gervais, D Meillet, et al.
Human Molecular Genetics|July 1, 1994
Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiaeC Tribioli, M Mancini, E Plassart, et al.
Journal of the Neurological Sciences|October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneE Plassart, B Eymard, L Maurs, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Genes with triplet repeats: a new class of mutations causing neurological diseasesE Plassart, B Fontaine
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|January 1, 1976
[Respiratory movements during sleep of the neonate at term: comparison of thoracic and abdominal recordings]L Curzi-Dascalova, E Plassart
Early Human Development|April 1, 1978
Respiratory and motor events in sleeping infants: their correlation with thoracico-abdominal respiratory relationshipsL Curzi-Dascalova, E Plassart
Brain Research. Brain Research Reviews|December 18, 2001
Neurosteroids: recent findingsE Plassart-Schiess, E E Baulieu
Molecular Aspects of Medicine|April 30, 1998
Diseases caused by voltage-gated ion channelsB Fontaine, E Plassart-Schiess, S Nicole
Annals of Clinical Biochemistry|February 17, 1998
Apolipoprotein E polymorphism in multiple sclerosisA Gervais, O Gaillard, E Plassart, et al.
The Journal of Physiology|May 23, 1998
Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell lineE Plassart-Schiess, L Lhuillier, A L George, et al.
Journal of the Neurological Sciences|August 14, 1998
Apolipoprotein E and multiple sclerosis: a biochemical and genetic investigationO Gaillard, A Gervais, D Meillet, et al.
Human Molecular Genetics|July 1, 1994
Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiaeC Tribioli, M Mancini, E Plassart, et al.
Journal of the Neurological Sciences|October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneE Plassart, B Eymard, L Maurs, et al.
Pageof 2