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Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2014
Cognitive impairment in rapid-onset dystonia-parkinsonismJared F Cook, Deborah F Hill, Beverly M Snively, et al.
Neurology|August 31, 2012
Psychiatric disorders in rapid-onset dystonia-parkinsonismAllison Brashear, Jared F Cook, Deborah F Hill, et al.
Neurobiology of Disease|August 20, 2019
Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competitionElena Arystarkhova, Ihtsham U Haq, Timothy Luebbert, et al.
Neurology|November 3, 2017
Efficacy and safety of abobotulinumtoxinA in spastic lower limb: Randomized trial and extensionJean-Michel Gracies, Alberto Esquenazi, Allison Brashear, et al.
Neuron|July 21, 2004
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonismPatricia de Carvalho Aguiar, Kathleen J Sweadner, John T Penniston, et al.
The Lancet. Neurology|April 18, 2014
Distinct neurological disorders with ATP1A3 mutationsErin L Heinzen, Alexis Arzimanoglou, Allison Brashear, et al.
Epilepsia|February 7, 2015
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephalyAlex R Paciorkowski, Sharon S McDaniel, Laura A Jansen, et al.
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