PubMed

Polygenic Risk Variants for Type 2 Diabetes Susceptibility Modify Age at Diagnosis in Monogenic HNF1A Diabetes.

Lango Allen H, Johansson S, Ellard S, Shields B, Hertel JK, Ræder H, Colclough K, Molven A, Frayling TM, Njølstad PR, Hattersley AT, Weedon MN.

Diabetes. 2009 Sep 30. [Epub ahead of print]PMID: 19794065 [PubMed - as supplied by publisher]Related articles

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes.

Torsvik J, Johansson S, Johansen A, Ek J, Minton J, Ræder H, Ellard S, Hattersley A, Pedersen O, Hansen T, Molven A, Njølstad PR.

Hum Genet. 2009 Sep 17. [Epub ahead of print]PMID: 19760265 [PubMed - as supplied by publisher]Related articles

A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet.

Raeder H, Shaw N, Netelenbos C, Bjerknes R.

Eur J Endocrinol. 2008 Dec;159 Suppl 1:S101-5. Epub 2008 Sep 5.PMID: 18775977 [PubMed - indexed for MEDLINE]Related articles

Lack of pancreatic body and tail in HNF1B mutation carriers.

Haldorsen IS, Vesterhus M, Raeder H, Jensen DK, Søvik O, Molven A, Njølstad PR.

Diabet Med. 2008 Jul;25(7):782-7.PMID: 18644064 [PubMed - indexed for MEDLINE]Related articles

Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young.

Vesterhus M, Haldorsen IS, Raeder H, Molven A, Njølstad PR.

J Clin Endocrinol Metab. 2008 Sep;93(9):3505-9. Epub 2008 Jul 1.PMID: 18593771 [PubMed - indexed for MEDLINE]Related articlesFree article

Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations.

Vesterhus M, Raeder H, Aurlien H, Gjesdal CG, Bredrup C, Holm PI, Molven A, Bindoff L, Berstad A, Njølstad PR.

Diabetes Care. 2008 Sep;31(9):1738-40. Epub 2008 Jun 10.PMID: 18544793 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Eide SA, Raeder H, Johansson S, Midthjell K, Søvik O, Njølstad PR, Molven A.

Diabet Med. 2008 Jul;25(7):775-81.PMID: 18513305 [PubMed - indexed for MEDLINE]Related articles

Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study).

Hertel JK, Johansson S, Raeder H, Midthjell K, Lyssenko V, Groop L, Molven A, Njølstad PR.

Diabetologia. 2008 Jun;51(6):971-7. Epub 2008 Apr 24.PMID: 18437351 [PubMed - indexed for MEDLINE]Related articles

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry.

Sagen JV, Bjørkhaug L, Molnes J, Raeder H, Grevle L, Søvik O, Molven A, Njølstad PR.

Pediatr Diabetes. 2008 Oct;9(5):442-9. Epub 2008 Apr 9.PMID: 18399931 [PubMed - indexed for MEDLINE]Related articles

Expression of N-methyl-d-aspartate (NMDA) receptor subunits and splice variants in an animal model of long-term voluntary alcohol self-administration.

Raeder H, Holter SM, Hartmann AM, Spanagel R, Moller HJ, Rujescu D.

Drug Alcohol Depend. 2008 Jul 1;96(1-2):16-21. Epub 2008 Mar 21.PMID: 18358639 [PubMed - indexed for MEDLINE]Related articles

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.

Molven A, Ringdal M, Nordbø AM, Raeder H, Støy J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, Joner G, Søvik O; Norwegian Childhood Diabetes Study Group, Bell GI, Njølstad PR.

Diabetes. 2008 Apr;57(4):1131-5. Epub 2008 Jan 11.PMID: 18192540 [PubMed - indexed for MEDLINE]Related articlesFree article

Pancreatic exocrine dysfunction in maturity-onset diabetes of the young type 3.

Vesterhus M, Raeder H, Johansson S, Molven A, Njølstad PR.

Diabetes Care. 2008 Feb;31(2):306-10. Epub 2007 Nov 5.PMID: 17989309 [PubMed - indexed for MEDLINE]Related articlesFree article

[50-year-old man with fatigue and monoclonal gammopaty]

Raeder H, Kildahl-Andersen O, Stalsberg H.

Tidsskr Nor Laegeforen. 2007 Oct 18;127(20):2677-9. Norwegian. PMID: 17972388 [PubMed - indexed for MEDLINE]Related articles

Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians.

Johansson S, Raeder H, Eide SA, Midthjell K, Hveem K, Søvik O, Molven A, Njølstad PR.

Diabetes. 2007 Dec;56(12):3112-7. Epub 2007 Sep 7.PMID: 17827402 [PubMed - indexed for MEDLINE]Related articlesFree article

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase.

Raeder H, Haldorsen IS, Ersland L, Grüner R, Taxt T, Søvik O, Molven A, Njølstad PR.

Diabetes. 2007 Feb;56(2):444-9.PMID: 17259390 [PubMed - indexed for MEDLINE]Related articlesFree article

A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry.

Raeder H, Bjørkhaug L, Johansson S, Mangseth K, Sagen JV, Hunting A, Følling I, Johansen O, Bjørgaas M, Paus PN, Søvik O, Molven A, Njølstad PR.

Diabetes. 2006 Jun;55(6):1899-903.PMID: 16731861 [PubMed - indexed for MEDLINE]Related articlesFree article

A pharmacological model for psychosis based on N-methyl-D-aspartate receptor hypofunction: molecular, cellular, functional and behavioral abnormalities.

Rujescu D, Bender A, Keck M, Hartmann AM, Ohl F, Raeder H, Giegling I, Genius J, McCarley RW, Möller HJ, Grunze H.

Biol Psychiatry. 2006 Apr 15;59(8):721-9. Epub 2006 Jan 19.PMID: 16427029 [PubMed - indexed for MEDLINE]Related articles

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.

Raeder H, Johansson S, Holm PI, Haldorsen IS, Mas E, Sbarra V, Nermoen I, Eide SA, Grevle L, Bjørkhaug L, Sagen JV, Aksnes L, Søvik O, Lombardo D, Molven A, Njølstad PR.

Nat Genet. 2006 Jan;38(1):54-62. Epub 2005 Dec 20.PMID: 16369531 [PubMed - indexed for MEDLINE]Related articles

[Molecular diagnostics in diabetes mellitus]

Bjørkhaug L, Johansson S, Raeder H, Thorsby PM, Undlien DE, Søvik O, Molven A, Sagen JV, Njølstad PR.

Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2968-72. Review. Norwegian. PMID: 16276383 [PubMed - indexed for MEDLINE]Related articlesFree article

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.

Sagen JV, Raeder H, Hathout E, Shehadeh N, Gudmundsson K, Baevre H, Abuelo D, Phornphutkul C, Molnes J, Bell GI, Gloyn AL, Hattersley AT, Molven A, Søvik O, Njølstad PR.

Diabetes. 2004 Oct;53(10):2713-8.PMID: 15448106 [PubMed - indexed for MEDLINE]Related articlesFree article

[Too narrow boot]

Kildahl-Andersen O, Raeder H.

Tidsskr Nor Laegeforen. 2004 Aug 12;124(15):1935-7. Norwegian. No abstract available. PMID: 15318409 [PubMed - indexed for MEDLINE]Related articles

[Anticoagulation treatment in atrial fibrillation]

Raeder H, Kildahl-Andersen O.

Tidsskr Nor Laegeforen. 2002 Feb 28;122(6):651. Norwegian. No abstract available. PMID: 11998724 [PubMed - indexed for MEDLINE]Related articles

[A man with deep venous thrombosis, transient ischemic attacks and increasing sedimentation rate]

Raeder H, Kildahl-Andersen O.

Tidsskr Nor Laegeforen. 2002 Feb 20;122(5):507-10. Norwegian. No abstract available. PMID: 11961981 [PubMed - indexed for MEDLINE]Related articles

Unchanged 24 h ambulatory blood pressure during shjort-term salt restriction and salt repletion in normotensive volunteers.

Raeder H, Aaberg M, Omvik P.

Blood Press Monit. 1996 Feb;1(1):39-44.PMID: 10226200 [PubMed - as supplied by publisher]Related articles