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Clinical characterization of a presenilin 1 mutation (F177S) in a family with very early-onset Alzheimer's disease in the third decade of life.
Hausner, Lucrezia; Tschäpe, Jakob A; Schmitt, Hans Peter; Hentschel, Frank; Hartmann, Tobias; Frölich, Lutz.
Afiliación
  • Hausner L; Department of Geriatric Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany; Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
  • Tschäpe JA; Department of Neurodegeneration and Neurobiology, Saarland University, Saarbrueckken, Germany; Department of Neurology, Saarland University, Saarbrueckken, Germany.
  • Schmitt HP; Department of Neuropathology, University of Heidelberg, Heidelberg, Germany.
  • Hentschel F; Department of Neuroradiology, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
  • Hartmann T; Department of Neurodegeneration and Neurobiology, Saarland University, Saarbrueckken, Germany; Department of Neurology, Saarland University, Saarbrueckken, Germany.
  • Frölich L; Department of Geriatric Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany. Electronic address: lutz.froelich@zi-mannheim.de.
Alzheimers Dement ; 10(2): e27-39, 2014 Mar.
Article en En | MEDLINE | ID: mdl-23850332
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Salud de la Familia / Predisposición Genética a la Enfermedad / Presenilina-1 / Enfermedad de Alzheimer / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2014 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Salud de la Familia / Predisposición Genética a la Enfermedad / Presenilina-1 / Enfermedad de Alzheimer / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2014 Tipo del documento: Article País de afiliación: Alemania