tallózása szerző szerint "Pirker W"

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  • Rare variants in beta-Amyloid precursor protein (APP) and Parkinson's disease. 
    Schulte EC; Fukumori A; Mollenhauer B; Hor H; Arzberger T; Perneczky R; Kurz A; Diehl-Schmid J; Hull M; Lichtner P; Eckstein G; Zimprich A; Haubenberger D; Pirker W; Brucke T; Bereznai Benjamin; Molnar Mária Judit; Lorenzo-Betancor O; Pastor P; Peters A; Gieger C; Estivill X; Meitinger T; Kretzschmar HA; Trenkwalder C; Haass C; Winkelmann J (2015)
    Many individuals with Parkinson's disease (PD) develop cognitive deficits, and a phenotypic and molecular overlap between neurodegenerative diseases exists. We investigated the contribution of rare variants in seven genes ...
  • Rare Variants in PLXNA4 and Parkinson's Disease. 
    Schulte EC; Stahl I; Czamara D; Ellwanger DC; Eck S; Graf E; Mollenhauer B; Zimprich A; Lichtner P; Haubenberger D; Pirker W; Brucke T; Bereznai Benjamin; Molnár Mária Judit; Peters A; Gieger C; Muller-Myhsok B; Trenkwalder C; Winkelmann J (2013)
    Approximately 20% of individuals with Parkinson's disease (PD) report a positive family history. Yet, a large portion of causal and disease-modifying variants is still unknown. We used exome sequencing in two affected ...
  • The role of SCARB2 as susceptibility factor in Parkinson's disease 
    Hopfner F; Schulte EC; Mollenhauer B; Bereznai Benjamin; Knauf F; Lichtner P; Zimprich A; Haubenberger D; Pirker W; Brucke T; Peters A; Gieger C; Kuhlenbaumer G; Trenkwalder C; Winkelmann J (2013)
    Background Genetic variation in the glucocerebrosidase (GBA) gene is strongly associated with Parkinson's disease (PD). Transport of glucocerebrosidase to the lysosome involves the protein encoded by the SCARB2 gene. An ...
  • Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease 
    Schulte E C; Mollenhauer B; Zimprich A; Bereznai Benjamin; Lichtner P; Haubenberger D; Pirker W; Brücke T; Molnar M J; Peters A; Gieger C; Trenkwalder C; Winkelmann J (2012)