Christesen HBT - Search Results

1

Prenatal and early postnatal exposure to perfluoroalkyl substances and bone mineral content and density in the Odense Child Cohort.

Højsager FD, Sigvaldsen A, Andersen MS, Juul A, Nielsen F, Möller S, Christesen HBT, Grøntved A, Grandjean P, Jensen TK. Højsager FD, et al. Among authors: christesen hbt. Environ Int. 2023 Nov;181:108264. doi: 10.1016/j.envint.2023.108264. Epub 2023 Oct 13. Environ Int. 2023. PMID: 37864903 Free article.

2

The topographical and laminar organization of a commissural-associational entorhino-entorhinal projection in the guinea pig.

Christesen HB, Sørensen KE. Christesen HB, et al. Brain Res. 1989 Dec 25;505(1):75-82. doi: 10.1016/0006-8993(89)90117-0. Brain Res. 1989. PMID: 2611680

3

Vitamin D status in pregnancy and childhood associates with intelligence quotient at age 7 years: An Odense child cohort study.

Cantio E, Bilenberg N, Nørgaard SM, Beck IH, Möller S, Cantio C, Jensen TK, Mortensen NB, Rasmussen A, Christesen HBT. Cantio E, et al. Among authors: christesen hbt. Aust N Z J Psychiatry. 2023 Jul;57(7):1062-1072. doi: 10.1177/00048674221116027. Epub 2022 Aug 15. Aust N Z J Psychiatry. 2023. PMID: 35971641

4

Vitamin D status in pregnancy and cord blood is associated with symptoms of attention-deficit hyperactivity disorder at age 5 years: Results from Odense Child Cohort.

Thinggaard CM, Dalgård C, Möller S, Christesen HBT, Bilenberg N. Thinggaard CM, et al. Among authors: christesen hbt. Aust N Z J Psychiatry. 2024 Dec;58(12):1090-1102. doi: 10.1177/00048674241272018. Epub 2024 Aug 16. Aust N Z J Psychiatry. 2024. PMID: 39152569

5

Prolonged elimination of tolbutamide in a premature newborn with hyperinsulinaemic hypoglycaemia.

Christesen HB, Melander A. Christesen HB, et al. Eur J Endocrinol. 1998 Jun;138(6):698-701. doi: 10.1530/eje.0.1380698. Eur J Endocrinol. 1998. PMID: 9678539

6

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

7

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. 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

8

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

9

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

10

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. 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

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