Raeder H - Search Results

1

Abnormal exocrine-endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8.

Kahraman S, Dirice E, Basile G, Diegisser D, Alam J, Johansson BB, Gupta MK, Hu J, Huang L, Soh CL, Huangfu D, Muthuswamy SK, Raeder H, Molven A, Kulkarni RN. Kahraman S, et al. Among authors: raeder h. Nat Metab. 2022 Jan;4(1):76-89. doi: 10.1038/s42255-021-00516-2. Epub 2022 Jan 20. Nat Metab. 2022. PMID: 35058633

2

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. Sagen JV, et al. Among authors: raeder h. Diabetes. 2004 Oct;53(10):2713-8. doi: 10.2337/diabetes.53.10.2713. Diabetes. 2004. PMID: 15448106

3

[Molecular diagnostics in diabetes mellitus].

Bjørkhaug L, Johansson S, Raeder H, Thorsby PM, Undlien DE, Søvik O, Molven A, Sagen JV, Njølstad PR. Bjørkhaug L, et al. Among authors: raeder h. Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2968-72. Tidsskr Nor Laegeforen. 2005. PMID: 16276383 Free article. Review. Norwegian.

4

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. Raeder H, et al. Nat Genet. 2006 Jan;38(1):54-62. doi: 10.1038/ng1708. Epub 2005 Dec 20. Nat Genet. 2006. PMID: 16369531

5

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. Raeder H, et al. Diabetes. 2006 Jun;55(6):1899-903. doi: 10.2337/db05-1677. Diabetes. 2006. PMID: 16731861

6

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. Raeder H, et al. Diabetes. 2007 Feb;56(2):444-9. doi: 10.2337/db06-0859. Diabetes. 2007. PMID: 17259390

7

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. Johansson S, et al. Among authors: raeder h. Diabetes. 2007 Dec;56(12):3112-7. doi: 10.2337/db07-0513. Epub 2007 Sep 7. Diabetes. 2007. PMID: 17827402

8

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

Vesterhus M, Raeder H, Johansson S, Molven A, Njølstad PR. Vesterhus M, et al. Among authors: raeder h. Diabetes Care. 2008 Feb;31(2):306-10. doi: 10.2337/dc07-1002. Epub 2007 Nov 5. Diabetes Care. 2008. PMID: 17989309

9

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. Molven A, et al. Among authors: raeder h. Diabetes. 2008 Apr;57(4):1131-5. doi: 10.2337/db07-1467. Epub 2008 Jan 11. Diabetes. 2008. PMID: 18192540

10

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. Sagen JV, et al. Among authors: raeder h. Pediatr Diabetes. 2008 Oct;9(5):442-9. doi: 10.1111/j.1399-5448.2008.00399.x. Epub 2008 Apr 9. Pediatr Diabetes. 2008. PMID: 18399931

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