Diemer B, Iversen N, Othman L, Hempel EL, Chaireti R, Bremme K(2026) Risk stratification according to genotype and effect of thromboprophylaxis on obstetric outcomes in women with antithrombin deficiency Res Pract Thromb Haemost, 10(4), 106637 DOI 10.1016/j.rpth.2026.106637, PubMed 42254458
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
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
