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5. Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family. Kabakci K; Isbruch K; Schilling K; Hedrich K; de Carvalho Aguiar P; Ozelius LJ; Kramer PL; Schwarz MH; Klein C J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):860-2. PubMed ID: 15897512 [TBL] [Abstract][Full Text] [Related]
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11. Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Wilhelmsen KC; Weeks DE; Nygaard TG; Moskowitz CB; Rosales RL; dela Paz DC; Sobrevega EE; Fahn S; Gilliam TC Ann Neurol; 1991 Feb; 29(2):124-31. PubMed ID: 1672807 [TBL] [Abstract][Full Text] [Related]
16. PET imaging of the pre-synaptic dopamine uptake sites in rapid-onset dystonia-parkinsonism (RDP). Brashear A; Mulholland GK; Zheng QH; Farlow MR; Siemers ER; Hutchins GD Mov Disord; 1999 Jan; 14(1):132-7. PubMed ID: 9918356 [TBL] [Abstract][Full Text] [Related]
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19. Dopa-responsive dystonia or early-onset Parkinson disease - Genotype-phenotype correlation. Potulska-Chromik A; Hoffman-Zacharska D; Łukawska M; Kostera-Pruszczyk A Neurol Neurochir Pol; 2017; 51(1):1-6. PubMed ID: 27667361 [TBL] [Abstract][Full Text] [Related]
20. A family with hereditary juvenile dystonia-parkinsonism. Ishikawa A; Miyatake T Mov Disord; 1995 Jul; 10(4):482-8. PubMed ID: 7565830 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]