Works matching AU Njølstad, P. R.

Results: 20

Familial non-immune hydrops fetalis and congenital pulmonary lymphangiectasia.

Published in:

1998

By:

Njølstad, P. R.;
Reigstad, H.;
Westby, J.;
Espeland, A.;
Njølstad, P R

Publication type:

journal article

Causes of death in childhood-onset Type 1 diabetes: long-term follow-up.

Published in:

Diabetic Medicine, 2017, v. 34, n. 1, p. 56, doi. 10.1111/dme.13114

By:

Gagnum, V.;
Stene, L. C.;
Jenssen, T. G.;
Berteussen, L. M.;
Sandvik, L.;
Joner, G.;
Njølstad, P. R.;
Skrivarhaug, T.

Publication type:

Article

Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young ( HNF1B- MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas.

Published in:

2013

By:

Tjora, E.;
Wathle, G.;
Erchinger, F.;
Engjom, T.;
Molven, A.;
Aksnes, L.;
Haldorsen, I. S.;
Dimcevski, G.;
Ræder, H.;
Njølstad, P. R.

Publication type:

Journal Article

Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young ( HNF1B- MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas.

Published in:

Diabetic Medicine, 2013, v. 30, n. 8, p. 946, doi. 10.1111/dme.12190

By:

Tjora, E.;
Wathle, G.;
Erchinger, F.;
Engjom, T.;
Molven, A.;
Aksnes, L.;
Haldorsen, I. S.;
Dimcevski, G.;
Ræder, H.;
Njølstad, P. R.

Publication type:

Article

Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study).

Published in:

Diabetic Medicine, 2008, v. 25, n. 7, p. 775, doi. 10.1111/j.1464-5491.2008.02459.x

By:

Eide, S. Å.;
Ræder, H.;
Johansson, S.;
Midthjell, K.;
Søvik, O.;
Njølstad, P. R.;
Molven, A.

Publication type:

Article

Lack of pancreatic body and tail in HNF1B mutation carriers.

Published in:

Diabetic Medicine, 2008, v. 25, n. 7, p. 782, doi. 10.1111/j.1464-5491.2008.02460.x

By:

Haldorsen, I. S.;
Vesterhus, M.;
Ræder, H.;
Jensen, D. K.;
Søvik, O.;
Molven, A.;
Njølstad, P. R.

Publication type:

Article

Are family factors universally related to metabolic outcomes in adolescents with Type 1 diabetes?

Published in:

Diabetic Medicine, 2008, v. 25, n. 4, p. 463, doi. 10.1111/j.1464-5491.2008.02399.x

By:

Cameron, F. J.;
Skinner, T. C.;
de Beaufort, C. E.;
Hoey, H.;
Swift, P. G. F.;
Aanstoot, H.;
Åman, J.;
Martul, P.;
Chiarelli, F.;
Daneman, D.;
Danne, T.;
Dorchy, H.;
Kaprio, E. A.;
Kaufman, F.;
Kocova, M.;
Mortensen, H. B.;
Njølstad, P. R.;
Phillip, M.;
Robertson, K. J.;
Schoenle, E. J.

Publication type:

Article

Clinical characteristics of mutation carriers in a large family with glucokinase diabetes (MODY2).

Published in:

Diabetic Medicine, 2005, v. 22, n. 8, p. 994, doi. 10.1111/j.1464-5491.2005.01555.x

By:

Shehadeh, N.;
Bakri, D.;
Njølstad, P. R.;
Gershoni-Baruch, R.

Publication type:

Article

Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus.

Published in:

Diabetic Medicine, 2005, v. 22, n. 8, p. 1012, doi. 10.1111/j.1464-5491.2005.01565.x

By:

Sagen, J. V.;
Baumann, M. E.;
Salvesen, H. B.;
Molven, A.;
Søvik, O.;
Njølstad, P. R.

Publication type:

Article

Preserved insulin response to tolbutamide in hepatocyte nuclear factor-1α mutation carriers.

Published in:

Diabetic Medicine, 2005, v. 22, n. 4, p. 406, doi. 10.1111/j.1464-5491.2005.01439.x

By:

Sagen, J. V.;
Pearson, E. R.;
Johansen, A.;
Spyer, G.;
Søvik, O.;
Pedersen, O.;
Njølstad, P. R.;
Hattersley, A. T.;
Hansen, T.

Publication type:

Article

Reduced prevalence of late-diabetic complications in MODY3 with early diagnosis.

Published in:

2002

By:

Sagen, J V;
Njølstad, P R;
Søvik, O

Publication type:

Journal Article

Reduced prevalence of late-diabetic complications in MODY3 with early diagnosis.

Published in:

Diabetic Medicine, 2002, v. 19, n. 8, p. 697, doi. 10.1046/j.1464-5491.2002.00688_1.x

By:

Sagen, J. V.;
Njølstad, P. R.;
Søvik, O.

Publication type:

Article

The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.

Published in:

Clinical Genetics, 2009, v. 75, n. 5, p. 440, doi. 10.1111/j.1399-0004.2009.01152.x

By:

Sandal, T.;
Laborie, L. B.;
Brusgaard, K.;
Eide, S.;
Christesen, H. B. T;
Søvik, O;
Njølstad, P. R.;
Molven, A.

Publication type:

Article

Target setting in intensive insulin management is associated with metabolic control: the Hvidoere Childhood Diabetes Study Group Centre Differences Study 2005.

Published in:

Pediatric Diabetes, 2010, v. 11, n. 4, p. 271, doi. 10.1111/j.1399-5448.2009.00596.x

By:

Swift, P. G. F.;
Skinner, T. C.;
de Beaufort, C. E.;
Cameron, F. J.;
Åman, J.;
Aanstoot, H.-J.;
Castaño, L.;
Chiarelli, F.;
Daneman, D.;
Danne, T.;
Dorchy, H.;
Hoey, H.;
Kaprio, E. A.;
Kaufman, F.;
Kocova, M.;
Mortensen, H. B.;
Njølstad, P. R.;
Phillip, M.;
Robertson, K. J.;
Schoenle, E. J.

Publication type:

Article

A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young.

Published in:

1998

By:

Njølstad, PR;
Cockburn, BN;
Bell, GI;
Søvik, O;
Njølstad, P R;
Cockburn, B N;
Bell, G I;
Søvik, O

Publication type:

journal article

The genetic abnormality in the beta cell determines the response to an oral glucose load.

Published in:

Diabetologia, 2002, v. 45, n. 3, p. 427, doi. 10.1007/s00125-001-0770-9

By:

Stride, A.;
Vaxillaire, M.;
Tuomi, T.;
Barbetti, F.;
Njølstad, P. R.;
Hansen, T.;
Costa, A.;
Conget, I.;
Pedersen, O.;
Søvik, O.;
Lorini, R.;
Groop, L.;
Froguel, P.;
Hattersley, A. T.

Publication type:

Article

A simple test for the high-frequency P291fsinsC mutation in the HNF1α/MODY3 gene.

Published in:

Diabetologia, 2000, v. 43, n. 6, p. 818

By:

Bjørkhaug, L.;
Søvik, O.;
Bell, G. I.;
Njølstad, P. R.;
Molven, A.

Publication type:

Article

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations.

Published in:

Genes & Immunity, 2012, v. 13, n. 5, p. 431, doi. 10.1038/gene.2012.11

By:

Eike, M C;
Skinningsrud, B;
Ronninger, M;
Stormyr, A;
Kvien, T K;
Joner, G;
Njølstad, P R;
Førre, Ø;
Flatø, B;
Alfredsson, L;
Padyukov, L;
Undlien, D E;
Lie, B A

Publication type:

Article

A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma.

Published in:

Genes & Immunity, 2009, v. 10, n. 2, p. 181, doi. 10.1038/gene.2008.100

By:

Bjørnvold, M.;
Munthe-Kaas, M. C.;
Egeland, T.;
Joner, G.;
Dahl-Jørgensen, K.;
Njølstad, P. R.;
Akselsen, H. E.;
Gervin, K.;
Carlsen, K. C. L.;
Carlsen, K. H.;
Undlien, D. E.

Publication type:

Article

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.

Published in:

Genes & Immunity, 2009, v. 10, n. 2, p. 120, doi. 10.1038/gene.2008.85

By:

Magitta, N. F.;
Bøe Wolff, A. S.;
Johansson, S.;
Skinningsrud, B.;
Lie, B. A.;
Myhr, K.-M.;
Undlien, D. E.;
Joner, G.;
Njølstad, P. R.;
Kvien, T. K.;
Førre, Ø.;
Knappskog, P. M.;
Husebye, E. S.

Publication type:

Article