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Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.
Stättermayer, Albert Friedrich; Traussnigg, Stefan; Dienes, Hans-Peter; Aigner, Elmar; Stauber, Rudolf; Lackner, Karoline; Hofer, Harald; Stift, Judith; Wrba, Friedrich; Stadlmayr, Andreas; Datz, Christian; Strasser, Michael; Maieron, Andreas; Trauner, Michael; Ferenci, Peter.
Afiliação
  • Stättermayer AF; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Traussnigg S; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Dienes HP; Institute for Clinical Pathology, Medical University of Vienna, Vienna, Austria.
  • Aigner E; Department of Internal Medicine I, Paracelsus Private Medical University, Salzburg, Austria.
  • Stauber R; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Lackner K; Institute of Pathology, Medical University of Graz, Graz, Austria.
  • Hofer H; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Stift J; Institute for Clinical Pathology, Medical University of Vienna, Vienna, Austria.
  • Wrba F; Institute for Clinical Pathology, Medical University of Vienna, Vienna, Austria.
  • Stadlmayr A; Department of Internal Medicine, KH Oberndorf, Oberndorf, Austria.
  • Datz C; Department of Internal Medicine, KH Oberndorf, Oberndorf, Austria.
  • Strasser M; Department of Internal Medicine I, Paracelsus Private Medical University, Salzburg, Austria.
  • Maieron A; Department of Internal Medicine IV, KH der Elisabethinen, Linz, Austria.
  • Trauner M; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Ferenci P; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria. Electronic address: peter.ferenci@meduniwien.ac.at.
J Hepatol ; 63(1): 156-63, 2015 Jul.
Article em En | MEDLINE | ID: mdl-25678388
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Cobre / Degeneração Hepatolenticular / Lipase / Fígado / Proteínas de Membrana / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Cobre / Degeneração Hepatolenticular / Lipase / Fígado / Proteínas de Membrana / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article