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Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
Responsiveness to levodopa in epsilon-sarcoglycan deletionsMarta San Luciano, Laurie Ozelius, Katherine Sims, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic stormPuneet Opal, Ron Tintner, Joseph Jankovic, et al.Neurology|January 4, 2013
Metabolic changes in DYT11 myoclonus-dystoniaMaren Carbon, Deborah Raymond, Laurie Ozelius, et al.Pediatric Neurology|February 5, 2014
Alternating hemiplegia of childhood with a de novo mutation in ATP1A3 and changes in SLC2A1 responsive to a ketogenic dietAdriana Ulate-Campos, Carmen Fons, Rafael Artuch, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's diseaseVicki Shanker, Mark Groves, Gary Heiman, et al.JAMA|January 14, 2010
Association of a functional polymorphism in the cholesteryl ester transfer protein (CETP) gene with memory decline and incidence of dementiaAmy E Sanders, Cuiling Wang, Mindy Katz, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2011
Substantia nigra hyperechogenicity with LRRK2 G2019S mutationsNorbert Brüggemann, Johann Hagenah, Kaili Stanley, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2010
Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletionPatricia De Carvalho Aguiar, Tania Fuchs, Vanderci Borges, et al.Journal of Neurochemistry|May 19, 2004
TorsinB--perinuclear location and association with torsinAJeffrey W Hewett, Christoph Kamm, Heather Boston, et al.Neurobiology of Aging|July 22, 2017
Cognitive and motor functioning in elderly glucocerebrosidase mutation carriersEileen E Moran, Cuiling Wang, Mindy Katz, et al.Pageof 5