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Mark S. LeDoux
Mark S. LeDoux
Veracity Neuroscience LLC; Professor, University of Memphis
Verified email at memphis.edu - Homepage
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Cited by
Year
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
JM Lee, EM Ramos, JH Lee, T Gillis, JS Mysore, MR Hayden, SC Warby, ...
Neurology 78 (10), 690-695, 2012
4182012
Randomized controlled trial of ethyl-eicosapentaenoic acid in Huntington disease: the TREND-HD study
Huntington Study Group TREND-HD Investigators
Archives of neurology 65 (12), 1582-1589, 2008
2432008
Secondary cervical dystonia associated with structural lesions of the central nervous system
MS LeDoux, KA Brady
Movement disorders: official journal of the Movement Disorder Society 18 (1 …, 2003
2312003
The focal dystonias: current views and challenges for future research
HA Jinnah, A Berardelli, C Comella, G DeFazio, MR DeLong, S Factor, ...
Movement Disorders 28 (7), 926-943, 2013
2272013
Current opinions and areas of consensus on the role of the cerebellum in dystonia
VG Shakkottai, A Batla, K Bhatia, WT Dauer, C Dresel, M Niethammer, ...
The Cerebellum 16, 577-594, 2017
2162017
Randomized controlled trial of deutetrabenazine for tardive dyskinesia: the ARM-TD study
HH Fernandez, SA Factor, RA Hauser, J Jimenez-Shahed, WG Ondo, ...
Neurology 88 (21), 2003-2010, 2017
1902017
Mutations in CIZ1 cause adult onset primary cervical dystonia
J Xiao, RJ Uitti, Y Zhao, SR Vemula, JS Perlmutter, ZK Wszolek, ...
Annals of neurology 71 (4), 458-469, 2012
1862012
Efficacy and safety of incobotulinumtoxinA (NT 201, XEOMIN®, botulinum neurotoxin type A, without accessory proteins) in patients with cervical dystonia
CL Comella, J Jankovic, DD Truong, A Hanschmann, S Grafe, ...
Journal of the neurological sciences 308 (1-2), 103-109, 2011
1662011
Natural history of Huntington disease
ER Dorsey, CA Beck, K Darwin, P Nichols, AFD Brocht, KM Biglan, ...
JAMA neurology 70 (12), 1520-1530, 2013
1532013
A randomized, double‐blind, placebo‐controlled trial of pridopidine in Huntington's disease
Huntington Study Group HART Investigators
Movement Disorders 28 (10), 1407-1415, 2013
1512013
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
Y Jiao, J Yan, Y Zhao, LR Donahue, WG Beamer, X Li, BA Roe, ...
Genetics 171 (3), 1239-1246, 2005
1382005
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease
A McGarry, M McDermott, K Kieburtz, EA de Blieck, F Beal, K Marder, ...
Neurology 88 (2), 152-159, 2017
1352017
Neuropathology of cervical dystonia
CN Prudente, CA Pardo, J Xiao, J Hanfelt, EJ Hess, MS Ledoux, ...
Experimental neurology 241, 95-104, 2013
1342013
A randomized, double-blind, placebo-controlled study to assess the efficacy and tolerability of gabapentin enacarbil in subjects with restless legs syndrome
DO Lee, RB Ziman, AT Perkins, JS Poceta, AS Walters, RW Barrett, ...
Journal of Clinical Sleep Medicine 7 (3), 282-292, 2011
1242011
Characterization of a large group of individuals with Huntington disease and their relatives enrolled in the COHORT study
DE Huntington Study Group COHORT Investigators.
PLoS One 7 (2), e29522, 2012
1202012
Novel THAP1 sequence variants in primary dystonia
J Xiao, Y Zhao, RW Bastian, JS Perlmutter, BA Racette, SD Tabbal, ...
Neurology 74 (3), 229-238, 2010
1202010
Cerebellectomy eliminates the motor syndrome of the genetically dystonic rat
MS LeDoux, JF Lorden, JM Ervin
Experimental neurology 120 (2), 302-310, 1993
1201993
Safety, tolerability, and efficacy of PBT2 in Huntington's disease: a phase 2, randomised, double-blind, placebo-controlled trial
Huntington Study Group Reach2HD Investigators
The Lancet Neurology 14 (1), 39-47, 2015
1152015
Role of Gα (olf) in familial and sporadic adult-onset primary dystonia
SR Vemula, A Puschmann, J Xiao, Y Zhao, M Rudzińska, KP Frei, ...
Human molecular genetics 22 (12), 2510-2519, 2013
1142013
Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors
DH Heck, Y Zhao, S Roy, MS LeDoux, LT Reiter
Human molecular genetics 17 (14), 2181-2189, 2008
1142008
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