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(in press) DOI 10.1016/j.jtha.2025.03.001, PubMed 40086756
Iversen N, Henriksson CE, Sletten M, Le MS, Lindberg BR, Andersen R, Paus B(2024) Heterozygosity for the Budapest 3 mutation in SERPINC1 in a family with thrombophilia and structural anomalies of the inferior vena cava Thromb J, 22(1), 75 DOI 10.1186/s12959-024-00644-1, PubMed 39129027
Lind SM, Sletten M, Hellenes M, Mathelier A, Tekpli X, Tinholt M, Iversen N(2024) Coagulation factor V in breast cancer: a p53-regulated tumor suppressor and predictive marker for treatment response to chemotherapy J Thromb Haemost, 22(6), 1569-1582 DOI 10.1016/j.jtha.2024.02.008, PubMed 38382738
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