Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
Irgens, H. U., Molnes, J., Johansson, B. B., Ringdal, M., Skrivarhaug, T., Undlien, D. E., Søvik, O., Joner, G., Molven, A., Njølstad, P. R.
Published in Diabetologia (01.07.2013)
Published in Diabetologia (01.07.2013)
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Fear of hypoglycaemia in mothers and fathers of children with Type 1 diabetes is associated with poor glycaemic control and parental emotional distress: a population-based study
Haugstvedt, A., Wentzel-Larsen, T., Graue, M., Søvik, O., Rokne, B.
Published in Diabetic medicine (01.01.2010)
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Lack of pancreatic body and tail in HNF1B mutation carriers
Haldorsen, I. S., Vesterhus, M., Ræder, H., Jensen, D. K., Søvik, O., Molven, A., Njølstad, P. R.
Published in Diabetic medicine (01.07.2008)
Published in Diabetic medicine (01.07.2008)
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The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes
Sagen, J.V., Bjørkhaug, L., Haukanes, B.I., Grevle, L., Molnes, J., Nedrebø, B.G., Søvik, O., Njølstad, P.R., Johansson, S., Molven, A.
Published in Diabetes research and clinical practice (01.11.2017)
Published in Diabetes research and clinical practice (01.11.2017)
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The genetic abnormality in the beta cell determines the response to an oral glucose load
STRIDE, A, VAXILLAIRE, M, LORINI, R, GROOP, L, FROGUEL, P, HATTERSLEY, A. T, TUOMI, T, BARBETTI, F, NJØLSTAD, P. R, HANSEN, T, COSTA, A, CONGET, I, PEDERSEN, O, SØVIK, O
Published in Diabetologia (01.03.2002)
Published in Diabetologia (01.03.2002)
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Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)
Eide, S. Å., Ræder, H., Johansson, S., Midthjell, K., Søvik, O., Njølstad, P. R., Molven, A.
Published in Diabetic medicine (01.07.2008)
Published in Diabetic medicine (01.07.2008)
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Neonatal Diabetes Mellitus Due to Complete Glucokinase Deficiency
Njølstad, Pål R, Søvik, Oddmund, Cuesta-Muñoz, Antonio, Bjørkhaug, Lise, Massa, Ornella, Barbetti, Fabrizio, Undlien, Dag E, Shiota, Chiyo, Magnuson, Mark A, Molven, Anders, Matschinsky, Franz M, Bell, Graeme I
Published in The New England journal of medicine (24.05.2001)
Published in The New England journal of medicine (24.05.2001)
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A Novel Syndrome of Diabetes Mellitus, Renal Dysfunction and Genital Malformation Associated with a Partial Deletion of the Pseudo-POU Domain of Hepatocyte Nuclear Factor-1β
Lindner, Tom H., Njølstad, Pål R., Horikawa, Yukio, Bostad, Leif, Bell, Graeme I., Søvik, Oddmund
Published in Human molecular genetics (01.10.1999)
Published in Human molecular genetics (01.10.1999)
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Insulin management and metabolic control of Type 1 diabetes mellitus in childhood and adolescence in 18 countries
Mortensen, H.B., Robertson, K.J., Aanstoot, H.-J., Danne, T., Holl, R.W., Hougaard, P., Atchison, J.A., Chiarelli, F., Daneman, D., Dinesen, B., Dorchy, H., Garandeau, P., Greene, S., Hoey, H., Kaprio, E.A., Kocova, M., Martul, P., Matsuura, N., Schoenle, E.J., Søvik, O., Swift, P.G.F., Tsou, R.M., Vanelli, M., Åman, J.
Published in Diabetic medicine (01.09.1998)
Published in Diabetic medicine (01.09.1998)
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Persistent Differences Among Centers Over 3 Years in Glycemic Control and Hypoglycemia in a Study of 3,805 Children and Adolescents With Type 1 Diabetes From the Hvidøre Study Group
DANNE, Thomas, MORTENSEN, Henrik B, HOEY, Hilary, HOLL, Reinhard W, KAPRIO, Eero A, KOCOVA, Mirjana, MARTUL, Pedro, MATSUURA, Nobuo, ROBERTSON, Kenneth J, SCHOFNLE, Eugen J, SØVIK, Oddmund, SWIFT, Peter G. F, HOUGAARD, Philip, TSOU, Rosa M, VANELLI, Maurizio, AMAN, Jan, LYNGGAARD, Helle, AANSTOOT, Henk-Jan, CHIARELLI, Francesco, DANEMAN, Denis, DORCHY, Harry, GARANDEAU, Patrick, GREENE, Stephen A
Published in Diabetes care (01.08.2001)
Published in Diabetes care (01.08.2001)
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The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy
Sandal, T, Laborie, LB, Brusgaard, K, Eide, SÅ, Christesen, HBT, Søvik, O, Njølstad, PR, Molven, A
Published in Clinical genetics (01.05.2009)
Published in Clinical genetics (01.05.2009)
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Wolcott–Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome
Søvik, O., Njølstad, P. R., Jellum, E., Molven, A.
Published in Journal of inherited metabolic disease (01.12.2008)
Published in Journal of inherited metabolic disease (01.12.2008)
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