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Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor Phenotype.
Steinhardt, Julia; Hanssen, Henrike; Heldmann, Marcus; Sprenger, Andreas; Laabs, Björn-Hergen; Domingo, Aloysius; Reyes, Charles Jourdan; Prasuhn, Jannik; Brand, Max; Rosales, Raymond; Münte, Thomas F; Klein, Christine; Westenberger, Ana; Oropilla, Jean Q; Diesta, Cid; Brüggemann, Norbert.
  • Steinhardt J; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Hanssen H; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Heldmann M; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Sprenger A; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Laabs BH; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Domingo A; Institute of Medical Biometry and Statistics, University of Lübeck University Hospital Schleswig-Holstein, Lübeck, Germany.
  • Reyes CJ; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Prasuhn J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Brand M; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rosales R; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Münte TF; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Westenberger A; Department of Neurology and Psychiatry, University of Santo Thomas, Manila, Philippines.
  • Oropilla JQ; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Diesta C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Brüggemann N; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Mov Disord ; 37(7): 1474-1482, 2022 07.
Article en En | MEDLINE | ID: mdl-35491955
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Enfermedades Genéticas Ligadas al Cromosoma X Tipo de estudio: Prognostic_studies / Screening_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Enfermedades Genéticas Ligadas al Cromosoma X Tipo de estudio: Prognostic_studies / Screening_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article