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Parkinsonism & Related Disorders|October 16, 2012
Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson diseaseM J Barrett, J Hagenah, V Dhawan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 20, 2015
Low-variance RNAs identify Parkinson's disease molecular signature in bloodMaria D Chikina, Christophe P Gerald, Xianting Li, 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.
Molecular Genetics and Metabolism|November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the testR Saunders-Pullman, N Blau, K Hyland, et al.
Brain : a Journal of Neurology|December 20, 2012
Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonismBart F L van Nuenen, Rick C Helmich, Murielle Ferraye, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 27, 2015
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 geneAnat Mirelman, Roy N Alcalay, Rachel Saunders-Pullman, et al.
Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.
NPJ Parkinson'S Disease|December 7, 2023
Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's diseaseGabriel Miltenberger-Miltenyi, Roberto A Ortega, Aloysius Domingo, et al.
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