Your browser doesn't support javascript.
loading
Vitamin D receptor biochemical and genetic profiling and HLA-class II genotyping among Lebanese with multiple sclerosis - A pilot study.
Yamout, Bassem; Karaky, Nathalie M; Mahfouz, Rami A R; Jaber, Fadel; Estaitieh, Nour; Shamaa, Dina; Abbas, Fatmeh; Hoteit, Rouba; Daher, Rose T.
Afiliação
  • Yamout B; Multiple Sclerosis Center, Department of Neurology, American University of Beirut Medical Center, Lebanon.
  • Karaky NM; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Mahfouz RAR; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Jaber F; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Estaitieh N; Department of Neurology, American University of Beirut Medical Center, Lebanon.
  • Shamaa D; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Abbas F; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Hoteit R; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon.
  • Daher RT; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Lebanon. Electronic address: rd02@aub.edu.lb.
J Neuroimmunol ; 293: 59-64, 2016 Apr 15.
Article em En | MEDLINE | ID: mdl-27049563

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos HLA-DR / Receptores de Calcitriol / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Esclerose Múltipla Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos HLA-DR / Receptores de Calcitriol / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Esclerose Múltipla Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2016 Tipo de documento: Article