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Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.
Gatto, Emilia M; Allegri, Ricardo F; Da Prat, Gustavo; Chrem Mendez, Patricio; Hanna, David S; Dorschner, Michael O; Surace, Ezequiel I; Zabetian, Cyrus P; Mata, Ignacio F.
Afiliação
  • Gatto EM; Department of Movement Disorders, Fundación INEBA, Buenos Aires, Argentina; Department of Neurology, Sanatorio de la Trinidad Mitre, Buenos Aires, Argentina.
  • Allegri RF; Department of Cognitive Neurology, Memory and Aging Center, Instituto de Investigaciones Neurológicas Dr. Raúl Carrea (FLENI), Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Investigator at CONICET the Argentine Research Council (CONICET), Cdad. Autóno
  • Da Prat G; Department of Neurology, Sanatorio de la Trinidad Mitre, Buenos Aires, Argentina.
  • Chrem Mendez P; Department of Cognitive Neurology, Memory and Aging Center, Instituto de Investigaciones Neurológicas Dr. Raúl Carrea (FLENI), Buenos Aires, Argentina.
  • Hanna DS; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA; Department of Pathology, University of Washington, Seattle, WA, USA.
  • Dorschner MO; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA; Department of Pathology, University of Washington, Seattle, WA, USA.
  • Surace EI; Department of Neuropathology, Laboratorio de Biología Molecular, Instituto de Investigaciones Neurológicas Dr. Raúl Carrea (FLENI), Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Investigator at CONICET the Argentine Research Council (CONICET), Cdad. A
  • Zabetian CP; Geriatric Research Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, Seattle, WA, USA.
  • Mata IF; Geriatric Research Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, Seattle, WA, USA. Electronic address: nachofm@uw.edu.
Neurobiol Aging ; 53: 195.e11-195.e17, 2017 05.
Article em En | MEDLINE | ID: mdl-28268100
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas tau / Degeneração Lobar Frontotemporal / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Argentina Idioma: En Revista: Neurobiol Aging Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Argentina
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas tau / Degeneração Lobar Frontotemporal / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Argentina Idioma: En Revista: Neurobiol Aging Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Argentina