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@ARTICLE{Vglein:140900,
      author       = {Vöglein, Jonathan and Paumier, Katrina and Jucker, Mathias
                      and Preische, Oliver and McDade, Eric and Hassenstab, Jason
                      and Benzinger, Tammie L and Noble, James M and Berman, Sarah
                      B and Graff-Radford, Neill R and Ghetti, Bernardino and
                      Farlow, Martin R and Chhatwal, Jasmeer and Salloway, Stephen
                      and Xiong, Chengjie and Karch, Celeste M and Cairns, Nigel
                      and Mori, Hiroshi and Schofield, Peter R and Masters, Colin
                      L and Goate, Alison and Buckles, Virginia and Fox, Nick and
                      Rossor, Martin and Chrem, Patricio and Allegri, Ricardo and
                      Ringman, John M and Höglinger, Günter and Steiner, Harald
                      and Dieterich, Marianne and Haass, Christian and Laske,
                      Christoph and Morris, John C and Bateman, Randall J and
                      Danek, Adrian and Levin, Johannes and Network, Dominantly
                      Inherited Alzheimer},
      title        = {{C}linical, pathophysiological and genetic features of
                      motor symptoms in autosomal dominant {A}lzheimer's disease.},
      journal      = {Brain},
      volume       = {142},
      number       = {5},
      issn         = {0006-8950},
      address      = {Oxford},
      publisher    = {Oxford Univ. Press},
      reportid     = {DZNE-2020-07222},
      pages        = {1429-1440},
      year         = {2019},
      abstract     = {Clinical, pathophysiological and genetic features of motor
                      symptoms in autosomal dominant Alzheimer's disease.},
      keywords     = {Adult / Aged / Alzheimer Disease: epidemiology / Alzheimer
                      Disease: genetics / Alzheimer Disease: physiopathology /
                      Female / Heterozygote / Humans / Male / Middle Aged / Motor
                      Disorders: epidemiology / Motor Disorders: genetics / Motor
                      Disorders: physiopathology / Mutation: genetics},
      cin          = {AG Höglinger 1 / AG Jucker / AG Steiner / Clinical
                      Dementia Research München / AG Haass old / U Clinical
                      Researchers - München},
      ddc          = {610},
      cid          = {I:(DE-2719)1110002 / I:(DE-2719)1210001 /
                      I:(DE-2719)1110000-1 / I:(DE-2719)1111016 /
                      I:(DE-2719)1110007 / I:(DE-2719)7000003},
      pnm          = {342 - Disease Mechanisms and Model Systems (POF3-342) / 344
                      - Clinical and Health Care Research (POF3-344)},
      pid          = {G:(DE-HGF)POF3-342 / G:(DE-HGF)POF3-344},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:30897203},
      pmc          = {pmc:PMC6735903},
      doi          = {10.1093/brain/awz050},
      url          = {https://pub.dzne.de/record/140900},
}