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[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.
Discovery of molecular pathways mediating 1,25-dihydroxyvitamin D3 protection against cytokine-induced inflammation and damage of human and male mouse islets of Langerhans.
Wolden-Kirk H, Rondas D, Bugliani M, Korf H, Van Lommel L, Brusgaard K, Christesen HT, Schuit F, Proost P, Masini M, Marchetti P, Eizirik DL, Overbergh L, Mathieu C. Wolden-Kirk H, et al. Among authors: brusgaard k. Endocrinology. 2014 Mar;155(3):736-47. doi: 10.1210/en.2013-1409. Epub 2014 Jan 1. Endocrinology. 2014. PMID: 24424042 Free article.
Neonatal High Bone Mass With First Mutation of the NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65).
Frederiksen AL, Larsen MJ, Brusgaard K, Novack DV, Knudsen PJ, Schrøder HD, Qiu W, Eckhardt C, McAlister WH, Kassem M, Mumm S, Frost M, Whyte MP. Frederiksen AL, et al. Among authors: brusgaard k. J Bone Miner Res. 2016 Jan;31(1):163-72. doi: 10.1002/jbmr.2590. Epub 2015 Aug 6. J Bone Miner Res. 2016. PMID: 26178921 Free PMC article.
116 results