Dybedal I, Iversen N, Jacobsen AF, Bjørge L, Chaireti R, Henriksson CE, Schultz NH, Hvas AM, Sandset PM, Weedon-Fekjær H, Bremme K, Abildgaard U(2025) Hereditary antithrombin deficiency and venous thrombosis in pregnancy-results of a retrospective multicenter study J Thromb Haemost, 23(9), 2807-2818 DOI 10.1016/j.jtha.2025.03.001, PubMed 40086756
Hellum M, Sletten M, Le MS, Stavseth V, Glosli H, Backe PH, Iversen N, Henriksson CE(2025) Characterization of a novel factor X variant, p.F139L, associated with bleedings in heterozygous and compound heterozygous form Thromb Res, 253, 109412 DOI 10.1016/j.thromres.2025.109412, PubMed 40763424
Lind SM, Sletten M, Henriksson CE, Tinholt M, Iversen N(2025) Functional and Regulatory Effects of Factor V Leiden and Factor V rs6028 in Breast Cancer Genes (Basel), 16(7) DOI 10.3390/genes16070735, PubMed 40725392
Get in touch
Contact information Nina Iversen – uxnaiv@ous-hf.no, tlf 23016647/92834909 Visiting /postal address: Dept. Medical Genetics, Building 25, 1st floor (North), Ullevål Hospital, Kirkeveien 166, 0450 Oslo
