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Neurology|July 11, 2001
Evidence for familial aggregation of tremor in normal individualsE D Louis, B Ford, S Frucht, et al.Neurology|February 1, 1996
Cutaneous electromyographic silent period findings in brachial dystoniaS L Pullman, B Ford, B Elibol, et al.Archives of Neurology|May 1, 1996
Delayed-onset cerebellar syndromeE D Louis, T Lynch, B Ford, et al.Neurology|April 12, 2012
Network correlates of disease severity in multiple system atrophyK L Poston, C C Tang, T Eckert, et al.Annals of Neurology|June 21, 2001
Risk of tremor and impairment from tremor in relatives of patients with essential tremor: a community-based family studyE D Louis, B Ford, S Frucht, et al.Neurology|September 19, 2007
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson diseaseL N Clark, B M Ross, Y Wang, et al.Neurology|October 20, 2006
Frequency of LRRK2 mutations in early- and late-onset Parkinson diseaseL N Clark, Y Wang, E Karlins, et al.Neuroepidemiology|January 1, 1997
The Washington Heights-Inwood Genetic Study of Essential Tremor: methodologic issues in essential-tremor researchE D Louis, R Ottman, B Ford, et al.Advances in Neurology|January 1, 1983
Long-term treatment of tardive dyskinesia with presynaptically acting dopamine-depleting agentsS FahnPageof 90