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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.
Rattay, Tim W; Lindig, Tobias; Baets, Jonathan; Smets, Katrien; Deconinck, Tine; Söhn, Anne S; Hörtnagel, Konstanze; Eckstein, Kathrin N; Wiethoff, Sarah; Reichbauer, Jennifer; Döbler-Neumann, Marion; Krägeloh-Mann, Ingeborg; Auer-Grumbach, Michaela; Plecko, Barbara; Münchau, Alexander; Wilken, Bernd; Janauschek, Marc; Giese, Anne-Katrin; De Bleecker, Jan L; Ortibus, Els; Debyser, Martine; Lopez de Munain, Adolfo; Pujol, Aurora; Bassi, Maria Teresa; D'Angelo, Maria Grazia; De Jonghe, Peter; Züchner, Stephan; Bauer, Peter; Schöls, Ludger; Schüle, Rebecca.
Affiliation
  • Rattay TW; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, and Center for Neurology, University of Tübingen, Tübingen, Germany.
  • Lindig T; German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Baets J; Department of Diagnostic and Interventional Neuroradiology, University Hospital Tübingen, Tübingen, Germany.
  • Smets K; Neurogenetics Group, University of Antwerp, Antwerp, Belgium.
  • Deconinck T; Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Söhn AS; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.
  • Hörtnagel K; Neurogenetics Group, University of Antwerp, Antwerp, Belgium.
  • Eckstein KN; Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Wiethoff S; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.
  • Reichbauer J; Neurogenetics Group, University of Antwerp, Antwerp, Belgium.
  • Döbler-Neumann M; Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Krägeloh-Mann I; Department of Medical Genetics, Institute of Human Genetics, University of Tübingen, Tübingen, Germany.
  • Auer-Grumbach M; CeGaT GmbH, Tübingen, Germany.
  • Plecko B; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, and Center for Neurology, University of Tübingen, Tübingen, Germany.
  • Münchau A; German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Wilken B; Department of Psychiatry, University of Tübingen, Tübingen, Germany.
  • Janauschek M; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, and Center for Neurology, University of Tübingen, Tübingen, Germany.
  • Giese AK; German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • De Bleecker JL; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, and Center for Neurology, University of Tübingen, Tübingen, Germany.
  • Ortibus E; Department of Pediatric Neurology, University Children's Hospital, Tübingen, Germany.
  • Debyser M; Department of Pediatric Neurology, University Children's Hospital, Tübingen, Germany.
  • Lopez de Munain A; Department of Orthopaedics and Trauma-Surgery, Medical University Vienna, Vienna, Austria.
  • Pujol A; Division of Child Neurology, University Childrens Hospital Zurich, Zurich, Switzerland.
  • Bassi MT; Department of Pediatric and Adult Movement Disorders and Neuropsychiatry, Institute of Neurogenetics, University of Lübeck, Germany.
  • D'Angelo MG; Department of Neuropediatrics, Klinikum Kassel, Germany.
  • De Jonghe P; Department for Social Pediatrics, Kinderhospital Osnabrück, Germany.
  • Züchner S; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Bauer P; Department of Neurology, University Hospital Ghent, Ghent, Belgium.
  • Schöls L; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Schüle R; Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
Brain ; 142(6): 1561-1572, 2019 06 01.
Article in En | MEDLINE | ID: mdl-31135052
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Spastic Paraplegia, Hereditary / Heredodegenerative Disorders, Nervous System Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Brain Year: 2019 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Spastic Paraplegia, Hereditary / Heredodegenerative Disorders, Nervous System Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Brain Year: 2019 Document type: Article Affiliation country: