The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes von Sagen, J.V., Bjørkhaug, L., Haukanes, B.I., Grevle, L., Molnes, J., Nedrebø, B.G., Søvik, O., Njølstad, P.R., Johansson, S., Molven, A.

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Diabetes and necrotizing soft tissue infections—A prospective observational cohort study: Statistical analysis plan von Rosén, A., Arnell, P., Madsen, M. B., Nedrebø, B. G., Norrby‐Teglund, A., Hyldegaard, O., dos Santos, V. M., Bergey, F., Saccenti, E., Skrede, S., Trogen, Joakim, Aronsson, Sara, Sandström, Göran, Rosemar, Anders, Karlsson, Ylva, Nekludov, Michael, Helledie, Gladis, Hedetoft, Morten, Hansen, Bo, Polzik, Peter

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Phenotypic Variation in a Large Family with Autosomal Dominant Hypocalcaemia von Sørheim, J.I., Husebye, E.S., Nedrebø, B.G., Svarstad, E., Lind, J., Boman, H., Løvås, K.

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Plasma total homocysteine levels in hyperthyroid and hypothyroid patients von Nedrebø, B.G., Ericsson, U.-B., Nygård, O., Refsum, H., Ueland, P.M., Aakvaag, A., Aanderud, S., Lien, E.A.

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Phenotypic expression of the methylenetetrahydrofolate reductase 677C to T polymorphism and flavin cofactor availability in thyroid dysfunction von Hustad, S, Nedrebo, B.G, Ueland, P.M, Schneede, J, Vollset, S.E, Ulvik, A, Lien, E.A

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Epidemiology and health related quality of life in hypoparathyroidism in Norway von Astor, M.C, Løvås, K, Debowska, A, Eriksen, E.F, Evang, J.A, Fossum, C, Fougner, K.J, Holte, S.E, Lima, K, Moe, R.B, Myhre, A.G, Kemp, E.H, Nedrebø, B.G, Svartberg, J, Husebye, E.S

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