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E Plassart-Schiess

Showing results (1-10 of 5) with videos related to

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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
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 Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, et al.
Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
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
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 Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, et al.
Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.
Pageof 1