• Hemophagocytic lymphohistiocytosis and miliary tuberculosis in a previously healthy individual: a case report 

      Trovik, Linn; Sandnes, Miriam; Blomberg, Bjørn; Holmaas, Gunhild; Ahmed, Aymen B.; Tvedt, Tor Henrik Anderson; Vintermyr, Olav Karsten; Reikvam, Håkon (Journal article; Peer reviewed, 2020)
      Background Hemophagocytic lymphohistiocytosis (HLH) is a rare heterogenous genetic or acquired hyperinflammatory syndrome associated with a high degree of morbidity and mortality. HLH has clinical manifestations related ...
    • Hfe genotype, ferritin levels and transferrin saturation in patients with suspected hereditary hemochromatosis 

      Sandnes, Miriam; Vorland, Marta; Ulvik, Rune J.; Reikvam, Håkon (Journal article; Peer reviewed, 2021)
      HFE hemochromatosis is characterized by increased iron absorption and iron overload due to variants of the iron-regulating HFE gene. Overt disease is mainly associated with homozygosity for the C282Y variant, although the ...
    • Hyperferritinemi-katarakt-syndrom 

      Benneche, Andreas; Sandnes, Miriam; Bakke, Åsne; Reikvam, Håkon (Journal article; Peer reviewed, 2020)
    • Hyperferritinemia—a clinical overview 

      Sandnes, Miriam; Ulvik, Rune Johan; Vorland, Marta; Reikvam, Håkon (Journal article; Peer reviewed, 2021)
      Ferritin is one of the most frequently requested laboratory tests in primary and secondary care, and levels often deviate from reference ranges. Serving as an indirect marker for total body iron stores, low ferritin is ...