Browsing by Author "e99fae88-d7d5-4a8e-b83a-e7f148618709"

Now showing items 1-2 of 2

    • ATP13A2 variants in early-onset Parkinson's disease patients and controls 
      Djarmati, Ana; Hagenah, Johann; Reetz, Kathrin; Winkler, Susen; Behrens Pellegrino, María Isabel; Pawlack, Heike; Lohmann, Katja; Ramirez, Alfredo; Tadić, Vera; Brüggemann, Norbert; Berg, Daniela; Siebner, Hartwig R.; Lang, Anthony E.; Pramstaller, Peter P.; Binkofski, Ferdinand; (John Wiley and Sons Inc., 2009)
      Four genes responsible for recessively inherited forms of Parkinson's disease (PD) have been identified, including the recently discovered ATP13A2 (PARK9) gene. Our objective was to investigate the role of this gene in a ...
    • Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease 
      Butcher, Nancy J.; Marras, Connie; Pondal, Margarita; Rusjan, Pablo; Boot, Erik; Christopher, Leigh; Repetto, Gabriela M.; Fritsch, Rosemarie; Chow, Eva W.C.; Masellis, Mario; Strafella, Antonio P.; Lang, Anthony E.; Bassett, Anne S. (Oxford University Press, 2017)
      © The Author (2017). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.The recurrent 22q11.2 deletion is a genetic risk factor for early-onset Parkinson's disease. Adults with ...