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Journal of the Neurological Sciences|July 11, 2006
Rasagiline-associated motor improvement in PD occurs without worsening of cognitive and behavioral symptomsL Elmer, S Schwid, S Eberly, et al.
American Journal of Human Genetics|March 1, 1990
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritanceN J Risch, S B Bressman, D deLeon, et al.
Annals of Neurology|February 1, 1991
Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosomeK C Wilhelmsen, D E Weeks, T G Nygaard, et al.
Neurology|June 1, 1997
Secondary dystonia and the DYTI geneS B Bressman, D de Leon, D Raymond, et al.
Neurology|May 10, 2000
The DYT1 phenotype and guidelines for diagnostic testingS B Bressman, C Sabatti, D Raymond, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Neurochemical findings in neuroacanthocytosisJ G de Yebenes, M F Brin, M A Mena, 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.
Neurology|January 6, 2011
Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD studyR N Alcalay, A Siderowf, R Ottman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 1994
Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystoniaS B Bressman, A L Hunt, G A Heiman, et al.
Parkinsonism & Related Disorders|August 23, 2011
The relation between depression and parkin genotype: the CORE-PD studyA Srivastava, M-X Tang, H Mejia-Santana, et al.
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