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A novel PSEN1 mutation in a patient with sporadic early-onset Alzheimer's disease and prominent cerebellar ataxia.
Testi, Silvia; Peluso, Silvio; Fabrizi, Gian Maria; Antenora, Antonella; Russo, Cinzia Valeria; Pappatà, Sabina; Padovani, Alessandro; Ferrarini, Moreno; Filla, Alessandro.
Afiliação
  • Testi S; Department of Neurological and Movement Sciences, Section of Neuropathology, University of Verona, Italy.
  • Peluso S; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Fabrizi GM; Department of Neurological and Movement Sciences, Section of Neuropathology, University of Verona, Italy.
  • Antenora A; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Russo CV; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Pappatà S; Biostructure and Bioimaging Institute, CNR, Naples, Italy.
  • Padovani A; Clinical Neurology, Section for Neuromuscular Diseaseas and Neuropathies, University Hospital "Spedali Civili", Brescia, Italy.
  • Ferrarini M; Department of Neurological and Movement Sciences, Section of Neuropathology, University of Verona, Italy.
  • Filla A; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
J Alzheimers Dis ; 41(3): 709-14, 2014.
Article em En | MEDLINE | ID: mdl-24718101
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Presenilina-1 / Doença de Alzheimer / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Alzheimers Dis Assunto da revista: GERIATRIA / NEUROLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Presenilina-1 / Doença de Alzheimer / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Alzheimers Dis Assunto da revista: GERIATRIA / NEUROLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Itália