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Mitochondrial DNA G13708A variation and multiple sclerosis: Is there an association?
Andalib, S; Talebi, M; Sakhinia, E; Farhoudi, M; Sadeghi-Bazargani, H; Emamhadi, M R; Masoodian, N; Balaghi-Inalou, M; Vafaee, M S; Gjedde, A.
Afiliación
  • Andalib S; Neuroscience Research Center, Department of Neurosurgery, Poursina Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran. Electronic address: andalib@gums.ac.ir.
  • Talebi M; Neurosciences Research Center, Department of Neurology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Sakhinia E; Division of Medical Genetics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran; Division of Regenerative Medicine, School of Medicine, Faculty of Medical and Human Sciences, the University of Manchester, Manchester, UK.
  • Farhoudi M; Neurosciences Research Center, Department of Neurology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Sadeghi-Bazargani H; Department of Statistics and Epidemiology, School of Health, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Public Health Sciences, Karolina Institute, Stockholm, Sweden.
  • Emamhadi MR; Brachial Plexus and Peripheral Nerve Injury Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Masoodian N; Neurology Ward, Department of Internal Medicine, Kosar Hospital, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Balaghi-Inalou M; Department of Cardiology, Shahid Modarres Hospital, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Vafaee MS; Neurosciences Research Center, Department of Neurology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Psychiatry, University of Southern Denmark & Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
  • Gjedde A; Department of Neuroscience and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Rev Neurol (Paris) ; 173(3): 164-168, 2017 Mar.
Article en En | MEDLINE | ID: mdl-28341142
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Polimorfismo de Nucleótido Simple / Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Rev Neurol (Paris) Año: 2017 Tipo del documento: Article Pais de publicación: Francia
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Polimorfismo de Nucleótido Simple / Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Rev Neurol (Paris) Año: 2017 Tipo del documento: Article Pais de publicación: Francia