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@ARTICLE{Hglinger:140284,
      author       = {Höglinger, G. U. and Respondek, G. and Kovacs, G. G.},
      title        = {{N}ew classification of tauopathies.},
      journal      = {Revue neurologique},
      volume       = {174},
      number       = {9},
      issn         = {0035-3787},
      address      = {Issy-les-Moulineaux},
      publisher    = {Elsevier Masson},
      reportid     = {DZNE-2020-06606},
      pages        = {664-668},
      year         = {2018},
      abstract     = {Tauopathies are a group of neurodegenerative diseases
                      characterized by pathological intracellular deposits of the
                      protein tau. Isoform composition, morphology and anatomical
                      distribution of cellular tau-immunoreactivities are defining
                      distinct tauopathies as molecular pathological disease
                      entities. The clinical spectrum of tauopathies includes
                      syndromes with primary motor symptoms and with primary
                      cognitive dysfunction. The traditional syndrome-based
                      classification is currently being complemented by a
                      molecular-pathological classification. While the
                      syndrome-based classification is helpful to select
                      symptomatic therapies, and to generate clinical working
                      hypotheses about underlying etiologies, the
                      molecular-pathological classification is most important for
                      the development and application of molecularly tailored
                      disease-modifying therapies.},
      subtyp        = {Review Article},
      keywords     = {Humans / Neurodegenerative Diseases: classification /
                      Neurodegenerative Diseases: genetics / Supranuclear Palsy,
                      Progressive: classification / Supranuclear Palsy,
                      Progressive: genetics / Supranuclear Palsy, Progressive:
                      physiopathology / Tauopathies: classification / Tauopathies:
                      genetics / Tauopathies: physiopathology},
      cin          = {AG Höglinger 1},
      ddc          = {610},
      cid          = {I:(DE-2719)1110002},
      pnm          = {344 - Clinical and Health Care Research (POF3-344)},
      pid          = {G:(DE-HGF)POF3-344},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:30098799},
      doi          = {10.1016/j.neurol.2018.07.001},
      url          = {https://pub.dzne.de/record/140284},
}