Christesen HB - Search Results

1

Rapid genetic analysis in congenital hyperinsulinism.

Christesen HB, Brusgaard K, Alm J, Sjöblad S, Hussain K, Fenger C, Rasmussen L, Hovendal C, Otonkoski T, Jacobsen BB. Christesen HB, et al. Horm Res. 2007;67(4):184-8. doi: 10.1159/000097063. Epub 2006 Nov 15. Horm Res. 2007. PMID: 17114887

2

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. 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

3

[Congenital hyperinsulinism].

Christesen HB, Brusgaard K, Jacobsen BB. Christesen HB, et al. Ugeskr Laeger. 2001 Apr 23;163(17):2354-8. Ugeskr Laeger. 2001. PMID: 11347455 Review. Danish.

4

Pancreatic beta-cell stimulation tests in transient and persistent congenital hyperinsulinism.

Christesen HB, Feilberg-Jørgensen N, Jacobsen BB. Christesen HB, et al. Acta Paediatr. 2001 Oct;90(10):1116-20. doi: 10.1080/080352501317061495. Acta Paediatr. 2001. PMID: 11697420

5

Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studies.

Muzyamba M, Farzaneh T, Behe P, Thomas A, Christesen HB, Brusgaard K, Hussain K, Tinker A. Muzyamba M, et al. Among authors: christesen hb. Clin Endocrinol (Oxf). 2007 Jul;67(1):115-24. doi: 10.1111/j.1365-2265.2007.02847.x. Epub 2007 Apr 27. Clin Endocrinol (Oxf). 2007. PMID: 17466004

6

Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: hypoglycaemia unawareness and attacks.

Christesen HB, Brusgaard K, Beck Nielsen H, Brock Jacobsen B. Christesen HB, et al. Clin Endocrinol (Oxf). 2008 May;68(5):747-55. doi: 10.1111/j.1365-2265.2008.03184.x. Epub 2008 Jan 15. Clin Endocrinol (Oxf). 2008. PMID: 18208578

7

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: christesen hb. Clin Genet. 2009 May;75(5):440-8. doi: 10.1111/j.1399-0004.2009.01152.x. Clin Genet. 2009. PMID: 19475716

8

The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy.

Christesen HB, Jacobsen BB, Odili S, Buettger C, Cuesta-Munoz A, Hansen T, Brusgaard K, Massa O, Magnuson MA, Shiota C, Matschinsky FM, Barbetti F. Christesen HB, et al. Diabetes. 2002 Apr;51(4):1240-6. doi: 10.2337/diabetes.51.4.1240. Diabetes. 2002. PMID: 11916951

9

Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemia.

Alkhayyat H, Christesen HB, Steer J, Stewart H, Brusgaard K, Hussain K. Alkhayyat H, et al. Among authors: christesen hb. J Pediatr Endocrinol Metab. 2006 Dec;19(12):1451-7. doi: 10.1515/jpem.2006.19.12.1451. J Pediatr Endocrinol Metab. 2006. PMID: 17252699

10

Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinism.

Taneja TK, Mankouri J, Karnik R, Kannan S, Smith AJ, Munsey T, Christesen HB, Beech DJ, Sivaprasadarao A. Taneja TK, et al. Among authors: christesen hb. Hum Mol Genet. 2009 Jul 1;18(13):2400-13. doi: 10.1093/hmg/ddp179. Epub 2009 Apr 8. Hum Mol Genet. 2009. PMID: 19357197

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