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Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey.
Emekli, Inci; Tepgeç, Fatih; Samanci, Bedia; Toksoy, Güven; Hasanogullari Kina, Gizem; Tüfekçioglu, Zeynep; Basaran, Seher; Bilgiç, Basar; Gürvit, I Hakan; Emre, Murat; Uyguner, Zehra Oya; Hanagasi, Hasmet A.
Afiliação
  • Emekli I; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey. Electronic address: inci-sahin@hotmail.com.
  • Tepgeç F; Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Samanci B; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Toksoy G; Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Hasanogullari Kina G; Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Tüfekçioglu Z; Department of Neurology, Faculty of Medicine, Istanbul Aydin University, Istanbul, Turkey.
  • Basaran S; Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Bilgiç B; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Gürvit IH; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Emre M; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Uyguner ZO; Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Turkey.
  • Hanagasi HA; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
Parkinsonism Relat Disord ; 93: 35-39, 2021 12.
Article em En | MEDLINE | ID: mdl-34781237
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article