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Annals of Neurology|October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite familiesL Almasy, S B Bressman, D Raymond, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.
Annals of Neurology|October 29, 2002
Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutationsChristine Klein, Liu Liu, Dana Doheny, et al.
Neurology|August 22, 2022
Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S VariantRachel Saunders-Pullman, Roberto Angel Ortega, Cuiling Wang, et al.
Brain : a Journal of Neurology|February 7, 2007
The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 geneAllison Brashear, William B Dobyns, Patricia de Carvalho Aguiar, et al.
Annals of Neurology|January 26, 2012
Head injury, α-synuclein Rep1, and Parkinson's diseaseSamuel M Goldman, Freya Kamel, G Webster Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2019
Cervical dystonia incidence and diagnostic delay in a multiethnic populationSara C LaHue, Kathleen Albers, Samuel Goldman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 20, 2014
Peptidoglycan recognition protein genes and risk of Parkinson's diseaseSamuel M Goldman, Freya Kamel, G Webster Ross, et al.
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