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Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystoniaT Gasser, C M Bove, L J Ozelius, et al.Genomics|November 1, 1992
A genetic linkage map of human chromosome 9qL J Ozelius, D J Kwiatkowski, D E Schuback, et al.Annals of Neurology|May 19, 1998
Expression of the early-onset torsion dystonia gene (DYT1) in human brainS J Augood, J B Penney, I K Friberg, et al.Neuroscience Letters|April 23, 2011
Gender differences in the risk of familial parkinsonism: beyond LRRK2?R Saunders-Pullman, K Stanley, M San Luciano, et al.Annals of Human Genetics|March 30, 2000
Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern GermanyC Klein, P Vieregge, J Hagenah, et al.Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.Neurology|February 20, 1999
Genetic analysis of three patients with an 18p- syndrome and dystoniaC Klein, C E Page, P LeWitt, et al.Human Molecular Genetics|May 18, 2000
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cellsJ Hewett, C Gonzalez-Agosti, D Slater, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2005
Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new familyK Kabakci, K Isbruch, K Schilling, et al.Proceedings of the National Academy of Sciences of the United States of America|April 29, 1999
Association of a missense change in the D2 dopamine receptor with myoclonus dystoniaC Klein, M F Brin, P Kramer, et al.Pageof 7