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American Journal of Human Genetics|September 1, 1996
Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium testD E Grice, J F Leckman, D L Pauls, et al.
Neurology|August 29, 2001
Clinical markers of early disease in persons near onset of Huntington's diseaseJ S Paulsen, H Zhao, J C Stout, et al.
Neurology|February 14, 2007
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriersC W Hess, D Raymond, P de Carvalho Aguiar, et al.
American Journal of Human Genetics|February 1, 1991
Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genomeA J Pakstis, P Heutink, D L Pauls, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1996
A controlled trial of remacemide hydrochloride in Huntington's diseaseK Kieburtz, A Feigin, M McDermott, et al.
American Journal of Human Genetics|August 11, 2004
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility regionP Paschou, Y Feng, A J Pakstis, et al.
Pediatric Neurology|March 4, 2017
Design of a Multisite Study Assessing the Impact of Tic Disorders on Individuals, Families, and CommunitiesE F Augustine, H R Adams, R H Bitsko, et al.
Acta Neurologica Scandinavica|June 4, 2005
The prevalence of PD in a nutritionally deficient rural population in ChinaL Zhang, Z Y Nie, Y Liu, et al.
Neurology|January 26, 2006
Creatine in Huntington disease is safe, tolerable, bioavailable in brain and reduces serum 8OH2'dGS M Hersch, S Gevorkian, K Marder, et al.
American Journal of Human Genetics|October 7, 2000
A major locus for myoclonus-dystonia maps to chromosome 7q in eight familiesC Klein, K Schilling, R J Saunders-Pullman, et al.
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