Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up.
Pediatr Diabetes. 2012 Mar;13(2):155-62. doi: 10.1111/j.1399-5448.2011.00776.x. Epub 2011 Apr 24.
Pediatr Diabetes. 2012.
PMID: 21518169
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: eide sa.
Diabetes. 2007 Dec;56(12):3112-7. doi: 10.2337/db07-0513. Epub 2007 Sep 7.
Diabetes. 2007.
PMID: 17827402
Item in Clipboard
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.
Eide SA, et al.
Diabet Med. 2008 Jul;25(7):775-81. doi: 10.1111/j.1464-5491.2008.02459.x.
Diabet Med. 2008.
PMID: 18513305
Item in Clipboard
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: eide sa.
Nat Genet. 2006 Jan;38(1):54-62. doi: 10.1038/ng1708. Epub 2005 Dec 20.
Nat Genet. 2006.
PMID: 16369531
Item in Clipboard
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.
Sandal T, Laborie LB, Brusgaard K, Eide SA, Christesen HB, Søvik O, Njølstad PR, Molven A.
Sandal T, et al. Among authors: eide sa.
Clin Genet. 2009 May;75(5):440-8. doi: 10.1111/j.1399-0004.2009.01152.x.
Clin Genet. 2009.
PMID: 19475716
Item in Clipboard
Cite
Cite