Your browser doesn't support javascript.
loading
Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2.
Estanga, A; Rodriguez-Oroz, M C; Ruiz-Martinez, J; Barandiaran, M; Gorostidi, A; Bergareche, A; Mondragon, E; Lopez de Munain, A; Marti-Masso, J F.
Afiliación
  • Estanga A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain. Electronic address: ainara.estangaalustiza@osakidetza.net.
  • Rodriguez-Oroz MC; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Ikerbasque, Basque Foundation for Science, Bilbao, Spain.
  • Ruiz-Martinez J; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Barandiaran M; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Gorostidi A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain.
  • Bergareche A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Mondragon E; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain.
  • Lopez de Munain A; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain.
  • Marti-Masso JF; Neuroscience Unit, Biodonostia Research Institute, San Sebastian, Spain; Department of Neurology, University Hospital Donostia, San Sebastian, Spain; Department of Neuroscience, University of the Basque Country UPV/EHU, Spain.
Parkinsonism Relat Disord ; 20(10): 1097-100, 2014 Oct.
Article en En | MEDLINE | ID: mdl-25127457
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas Serina-Treonina Quinasas / Trastornos del Conocimiento / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas Serina-Treonina Quinasas / Trastornos del Conocimiento / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Reino Unido