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The International Journal of Neuroscience|February 19, 2016
Relapsing polychondritis complicated by cognitive dysfunction: two distinct clinical phenotypes?R J B Ellis, G K Mbizvo, A Jacob, et al.
The Journal of the Royal College of Physicians of Edinburgh|October 31, 2015
Rapid cognitive decline: not always Creutzfeldt-Jakob diseaseA Randall, R Ellis, B Hywel, et al.
Epilepsia|May 13, 1998
Complex partial status epilepticus in late-onset MELASA P Leff, A W McNabb, M G Hanna, et al.
European Journal of Neurology|September 14, 2001
Isolated familial hypomagnesaemia with novel neurological features: causal link or chance concurrence?A J Larner, C Williamson, N S Ward, et al.
Journal of the Neurological Sciences|November 11, 2003
Pathological heterogeneity of clinically diagnosed corticobasal degenerationM Doran, D G du Plessis, T P Enevoldson, et al.
Case Reports in Neurology|September 2, 2015
Facial Onset Sensory and Motor Neuronopathy: Further Evidence for a TDP-43 ProteinopathyBesa Ziso, Tim L Williams, R Jon L Walters, et al.
The American Journal of Medicine|January 17, 1983
Mediators of postreceptor action of insulinJ Larner
Brain : a Journal of Neurology|June 1, 1996
Focal upper limb demyelinating neuropathyP K Thomas, D Claus, A Jaspert, et al.
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