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Neurology|July 1, 1994
The phenotype of "pure" autosomal dominant spastic paraplegiaA Dürr, A Brice, M Serdaru, et al.Revue Neurologique|March 12, 2002
[Andermann syndrome in an Algerian family: suggestion of phenotype and genetic homogeneity]G Lesca, I Cournu-Rebeix, A Azoulay-Cayla, et al.Revue Neurologique|May 2, 2002
[Acute optic neuritis: clinical and MRI prognostic factors. Study of fifty patients]R Deschamps, O Gout, B Fontaine, et al.Journal of Neuroradiology = Journal De Neuroradiologie|September 1, 1996
In vivo localized NMR proton spectroscopy of normal appearing white matter in patients with multiple sclerosisA Tourbah, J L Stievenart, M T Iba-Zizen, et al.Journal of Autoimmunity|February 24, 2005
Hepatitis B vaccination and central nervous system demyelination: an immunological approachE Piaggio, A Ben Younes, S Desbois, et al.European Journal of Neurology|November 29, 2013
Frequency and relevance of IgM intrathecal synthesis in multiple sclerosisJ Reboul, P Lambin, A Gervais, et al.European Neurology|January 1, 1991
Observer disagreement in rating neurologic impairment in multiple sclerosis: facts and consequencesM H Verdier-Taillefer, M Zuber, O Lyon-Caen, et al.Neurology|August 3, 1999
Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS?A Tourbah, O Gout, R Liblau, et al.Neurology|October 29, 2003
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)F Portet, Y Dauvilliers, D Campion, et al.Nature|July 10, 1986
Analysis of human T-lymphotrophic virus sequences in multiple sclerosis tissueS L Hauser, C Aubert, J S Burks, et al.Pageof 19