Molven A - Search Results

1

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.

Christesen HB, Tribble ND, Molven A, Siddiqui J, Sandal T, Brusgaard K, Ellard S, Njølstad PR, Alm J, Brock Jacobsen B, Hussain K, Gloyn AL. Christesen HB, et al. Among authors: molven a. Eur J Endocrinol. 2008 Jul;159(1):27-34. doi: 10.1530/EJE-08-0203. Epub 2008 May 1. Eur J Endocrinol. 2008. PMID: 18450771

2

A zebrafish homologue of the murine Hox-2.1 gene.

Njølstad PR, Molven A, Fjose A. Njølstad PR, et al. Among authors: molven a. FEBS Lett. 1988 Mar 28;230(1-2):25-30. doi: 10.1016/0014-5793(88)80634-3. FEBS Lett. 1988. PMID: 2895022 Free article.

3

[The homeo box--a genetic key to fetal development].

Njølstad PR, Molven A. Njølstad PR, et al. Among authors: molven a. Tidsskr Nor Laegeforen. 1993 May 10;113(12):1475-9. Tidsskr Nor Laegeforen. 1993. PMID: 8101395 Review. Norwegian.

4

MODY associated with two novel hepatocyte nuclear factor-1alpha loss-of-function mutations (P112L and Q466X).

Bjørkhaug L, Ye H, Horikawa Y, Søvik O, Molven A, Njølstad PR. Bjørkhaug L, et al. Among authors: molven a. Biochem Biophys Res Commun. 2000 Dec 29;279(3):792-8. doi: 10.1006/bbrc.2000.4024. Biochem Biophys Res Commun. 2000. PMID: 11162430

5

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: molven a. 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.

6

Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.

Molven A, Rishaug U, Matre GE, Njølstad PR, Søvik O. Molven A, et al. Am J Med Genet. 2002 Nov 15;113(1):40-6. doi: 10.1002/ajmg.10575. Am J Med Genet. 2002. PMID: 12400064

7

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway.

Bjørkhaug L, Sagen JV, Thorsby P, Søvik O, Molven A, Njølstad PR. Bjørkhaug L, et al. Among authors: molven a. J Clin Endocrinol Metab. 2003 Feb;88(2):920-31. doi: 10.1210/jc.2002-020945. J Clin Endocrinol Metab. 2003. PMID: 12574234

8

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.

Njølstad PR, Sagen JV, Bjørkhaug L, Odili S, Shehadeh N, Bakry D, Sarici SU, Alpay F, Molnes J, Molven A, Søvik O, Matschinsky FM. Njølstad PR, et al. Among authors: molven a. Diabetes. 2003 Nov;52(11):2854-60. doi: 10.2337/diabetes.52.11.2854. Diabetes. 2003. PMID: 14578306

9

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.

Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njølstad PR, Jellum E, Søvik O. Molven A, et al. Diabetes. 2004 Jan;53(1):221-7. doi: 10.2337/diabetes.53.1.221. Diabetes. 2004. PMID: 14693719

10

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

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