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[Congenital hyperinsulinism].
Christesen HB, Brusgaard K, Jacobsen BB. Christesen HB, et al. Among authors: brusgaard k. Ugeskr Laeger. 2001 Apr 23;163(17):2354-8. Ugeskr Laeger. 2001. PMID: 11347455 Review. Danish.
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. Among authors: brusgaard k. Horm Res. 2007;67(4):184-8. doi: 10.1159/000097063. Epub 2006 Nov 15. Horm Res. 2007. PMID: 17114887
Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemia.
Alkhayyat H, Christesen HB, Steer J, Stewart H, Brusgaard K, Hussain K. Alkhayyat H, et al. Among authors: brusgaard k. 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
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: brusgaard k. 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
Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia.
McGlacken-Byrne SM, Mohammad JK, Conlon N, Gubaeva D, Siersbæk J, Schou AJ, Demirbilek H, Dastamani A, Houghton JAL, Brusgaard K, Melikyan M, Christesen H, Flanagan SE, Murphy NP, Shah P. McGlacken-Byrne SM, et al. Among authors: brusgaard k. Eur J Endocrinol. 2022 Feb 22;186(4):417-427. doi: 10.1530/EJE-21-0897. Eur J Endocrinol. 2022. PMID: 35089870
118 results