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Wilson's disease in Lebanon and regional countries: Homozygosity and hepatic phenotype predominance.
Barada, Kassem; El Haddad, Aline; Katerji, Meghri; Jomaa, Mustapha; Usta, Julnar.
Afiliação
  • Barada K; Department of Internal Medicine, American University of Beirut Medical Center, Beirut 110236, Lebanon.
  • El Haddad A; Department of Internal Medicine, American University of Beirut Medical Center, Beirut 110236, Lebanon.
  • Katerji M; Department of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut 110236, Lebanon.
  • Jomaa M; Department of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut 110236, Lebanon.
  • Usta J; Department of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut 110236, Lebanon. justa@aub.edu.lb.
World J Gastroenterol ; 23(36): 6715-6725, 2017 Sep 28.
Article em En | MEDLINE | ID: mdl-29085216

Texto completo: 1 Base de dados: MEDLINE Assunto principal: ATPases Transportadoras de Cobre / Degeneração Hepatolenticular / Homozigoto / Fígado Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País como assunto: Africa / Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: ATPases Transportadoras de Cobre / Degeneração Hepatolenticular / Homozigoto / Fígado Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País como assunto: Africa / Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article