Bell GI - Search Results

1

From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation.

Sagen JV, Odili S, Bjørkhaug L, Zelent D, Buettger C, Kwagh J, Stanley C, Dahl-Jørgensen K, de Beaufort C, Bell GI, Han Y, Grimsby J, Taub R, Molven A, Søvik O, Njølstad PR, Matschinsky FM. Sagen JV, et al. Among authors: bell gi. Diabetes. 2006 Jun;55(6):1713-22. doi: 10.2337/db05-1513. Diabetes. 2006. PMID: 16731834

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: bell gi. Diabetes. 2004 Oct;53(10):2713-8. doi: 10.2337/diabetes.53.10.2713. Diabetes. 2004. PMID: 15448106

3

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: bell gi. Diabetes. 2008 Apr;57(4):1131-5. doi: 10.2337/db07-1467. Epub 2008 Jan 11. Diabetes. 2008. PMID: 18192540

4

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

Njølstad PR, Cockburn BN, Bell GI, Søvik O. Njølstad PR, et al. Among authors: bell gi. Acta Paediatr. 1998 Aug;87(8):853-6. doi: 10.1080/080352598750013626. Acta Paediatr. 1998. PMID: 9736233

5

Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes.

Hathout E, Mace J, Bell GI, Njølstad PR. Hathout E, et al. Among authors: bell gi. Diabetes Care. 2006 Jun;29(6):1458. doi: 10.2337/dc06-0487. Diabetes Care. 2006. PMID: 16732049 No abstract available.

6

[Non-insulin dependent diabetes in children and adolescents].

Njølstad PR, Søvik O, Bell GI, Cockburn BN, Følling I, Sagen J. Njølstad PR, et al. Among authors: bell gi. Tidsskr Nor Laegeforen. 1998 Mar 10;118(7):1054-7. Tidsskr Nor Laegeforen. 1998. PMID: 9531829 Norwegian.

7

Exome sequencing and genetic testing for MODY.

Johansson S, Irgens H, Chudasama KK, Molnes J, Aerts J, Roque FS, Jonassen I, Levy S, Lima K, Knappskog PM, Bell GI, Molven A, Njølstad PR. Johansson S, et al. Among authors: bell gi. PLoS One. 2012;7(5):e38050. doi: 10.1371/journal.pone.0038050. Epub 2012 May 25. PLoS One. 2012. PMID: 22662265 Free PMC article.

8

Neonatal diabetes mellitus due to complete glucokinase deficiency.

Njølstad PR, Søvik O, Cuesta-Muñoz A, Bjørkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI. Njølstad PR, et al. Among authors: bell gi. N Engl J Med. 2001 May 24;344(21):1588-92. doi: 10.1056/NEJM200105243442104. N Engl J Med. 2001. PMID: 11372010 Free article. No abstract available.

9

Genetic variants of hepatocyte nuclear factor-1beta in Chinese young-onset diabetic patients with nephropathy.

So WY, Ng MC, Horikawa Y, Njølstad PR, Li JK, Ma RC, Bell GI, Chan JC. So WY, et al. Among authors: bell gi. J Diabetes Complications. 2003 Nov-Dec;17(6):369-73. doi: 10.1016/s1056-8727(02)00221-0. J Diabetes Complications. 2003. PMID: 14583183

10

Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2): different glucokinase defects lead to a common phenotype.

Miller SP, Anand GR, Karschnia EJ, Bell GI, LaPorte DC, Lange AJ. Miller SP, et al. Among authors: bell gi. Diabetes. 1999 Aug;48(8):1645-51. doi: 10.2337/diabetes.48.8.1645. Diabetes. 1999. PMID: 10426385

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