Showing results (191-200 of 312) with videos related to

Sort By:
Pageof 32
Neurology|April 1, 1993
Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor geneA A Amato, T W Prior, R J Barohn, et al.
Neurology|August 1, 1980
Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiencyS DiMauro, J R Mendell, Z Sahenk, et al.
Neurology|June 17, 1999
Definitive molecular diagnosis of facioscapulohumeral dystrophyR W Orrell, R Tawil, J Forrester, et al.
Neurology|June 6, 2008
Lack of toxicity of alpha-sarcoglycan overexpression supports clinical gene transfer trial in LGMD2DL R Rodino-Klapac, J-S Lee, R C Mulligan, et al.
Neurology|October 1, 1978
Quantitation of IgG, IgA and IgM in the CSF by radioimmunoassayE S Mingioli, W Strober, W W Tourtellotte, et al.
Neurology|November 18, 1998
Age-related changes in the level of urinary myelin basic protein-like material during childhoodA K Percy, J B Lane, J Goodwin, et al.
Clinical EEG (Electroencephalography)|January 1, 1982
Neuromyelitis optica (Devic's syndrome) in two sistersL T Ch'ien, M O Medeiros, J J Belluomini, et al.
Neurosurgery|September 12, 2000
Surgery for cervical spinal cord compression in patients with multiple sclerosisK Bashir, C Y Cai, T A Moore, et al.
Journal of Neuroimmunology|April 1, 1989
Monoclonal idiotypic and anti-idiotypic antibodies produced by immunization with peptides specified by a region of human myelin basic protein mRNA and its complementJ N Whitaker, B E Sparks, D P Walker, et al.
Neurology|September 10, 2003
Nonsystemic vasculitic neuropathy: insights from a clinical cohortM P Collins, M I Periquet, J R Mendell, et al.
Pageof 32