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Page 1
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.
Christesen HT, Christensen LG, Löfgren ÅM, Brøndum-Nielsen K, Svensson J, Brusgaard K, Samuelsson S, Elfving M, Jonson T, Grønskov K, Rasmussen L, Backman T, Hansen LK, Larsen AR, Petersen H, Detlefsen S. Christesen HT, et al. Among authors: brusgaard k. Eur J Med Genet. 2020 Jan;63(1):103632. doi: 10.1016/j.ejmg.2019.02.004. Epub 2019 Feb 21. Eur J Med Genet. 2020. PMID: 30797057 Free article.
Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.
Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ. Hussain K, et al. Among authors: brusgaard k. J Clin Endocrinol Metab. 2005 Jul;90(7):4376-82. doi: 10.1210/jc.2005-0158. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811927
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
Vitamin D and diabetes: its importance for beta cell and immune function.
Wolden-Kirk H, Overbergh L, Christesen HT, Brusgaard K, Mathieu C. Wolden-Kirk H, et al. Among authors: brusgaard k. Mol Cell Endocrinol. 2011 Dec 5;347(1-2):106-20. doi: 10.1016/j.mce.2011.08.016. Epub 2011 Aug 26. Mol Cell Endocrinol. 2011. PMID: 21889571 Review.
[Congenital hyperinsulinism--diagnosis and treatment].
Christesen HT, Bruun MF, Christoffersen SH, Rasmussen L, Petersen H, Detlefsen S, Hovendal CP, Hansen TG, Hansen TP, Brusgaard K. Christesen HT, et al. Among authors: brusgaard k. Ugeskr Laeger. 2011 Nov 21;173(47):3020-5. Ugeskr Laeger. 2011. PMID: 22118585 Review. Danish.
Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes.
Al Mutair AN, Brusgaard K, Bin-Abbas B, Hussain K, Felimban N, Al Shaikh A, Christesen HT. Al Mutair AN, et al. Among authors: brusgaard k. Diabetes Care. 2013 Mar;36(3):557-61. doi: 10.2337/dc12-1174. Epub 2012 Nov 12. Diabetes Care. 2013. PMID: 23150283 Free PMC article.
119 results