Grevle L - Search Results

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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. Among authors: grevle l. Nat Genet. 2006 Jan;38(1):54-62. doi: 10.1038/ng1708. Epub 2005 Dec 20. Nat Genet. 2006. PMID: 16369531

The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes.

Sagen JV, Bjørkhaug L, Haukanes BI, Grevle L, Molnes J, Nedrebø BG, Søvik O, Njølstad PR, Johansson S, Molven A. Sagen JV, et al. Among authors: grevle l. Diabetes Res Clin Pract. 2017 Nov;133:142-149. doi: 10.1016/j.diabres.2017.08.001. Epub 2017 Sep 1. Diabetes Res Clin Pract. 2017. PMID: 28934671

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: grevle l. 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

Allelic association between the DRD2 TaqI A polymorphism and Parkinson's disease.

Grevle L, Güzey C, Hadidi H, Brennersted R, Idle JR, Aasly J. Grevle L, et al. Mov Disord. 2000 Nov;15(6):1070-4. doi: 10.1002/1531-8257(200011)15:6<1070::aid-mds1003>3.0.co;2-a. Mov Disord. 2000. PMID: 11104188

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