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Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis.
Tripolszki, Kornélia; Csányi, Bernadett; Nagy, Dóra; Ratti, Antonia; Tiloca, Cinzia; Silani, Vincenzo; Kereszty, Éva; Török, Nóra; Vécsei, László; Engelhardt, József I; Klivényi, Péter; Nagy, Nikoletta; Széll, Márta.
Afiliação
  • Tripolszki K; Department of Medical Genetics, University of Szeged, Szeged, Hungary.
  • Csányi B; Department of Forensic Medicine, University of Szeged, Szeged, Hungary.
  • Nagy D; Department of Medical Genetics, University of Szeged, Szeged, Hungary.
  • Ratti A; Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy; Department of Pathophysiology and Transplantation, "Dino Ferrari" Center, Università degli Studi di Milano, Milan, Italy.
  • Tiloca C; Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.
  • Silani V; Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy; Department of Pathophysiology and Transplantation, "Dino Ferrari" Center, Università degli Studi di Milano, Milan, Italy.
  • Kereszty É; Department of Forensic Medicine, University of Szeged, Szeged, Hungary.
  • Török N; Department of Neurology, University of Szeged, Szeged, Hungary.
  • Vécsei L; Department of Neurology, University of Szeged, Szeged, Hungary; MTA-SZTE Neuroscience Research Group, University of Szeged, Szeged, Hungary.
  • Engelhardt JI; Department of Neurology, University of Szeged, Szeged, Hungary.
  • Klivényi P; Department of Neurology, University of Szeged, Szeged, Hungary.
  • Nagy N; Department of Medical Genetics, University of Szeged, Szeged, Hungary; MTA SZTE Dermatological Research Group, University of Szeged, Szeged, Hungary. Electronic address: nikoletta.nagy@gmail.com.
  • Széll M; Department of Medical Genetics, University of Szeged, Szeged, Hungary; MTA SZTE Dermatological Research Group, University of Szeged, Szeged, Hungary.
Neurobiol Aging ; 53: 195.e1-195.e5, 2017 05.
Article em En | MEDLINE | ID: mdl-28222900
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Estudos de Associação Genética / Superóxido Dismutase-1 / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurobiol Aging Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Hungria
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Estudos de Associação Genética / Superóxido Dismutase-1 / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurobiol Aging Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Hungria