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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Edghill EL, et al. Among authors: hussain k. Diabetes. 2008 Apr;57(4):1034-42. doi: 10.2337/db07-1405. Epub 2007 Dec 27. Diabetes. 2008. PMID: 18162506 Free PMC article.
The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia.
Roženková K, Güemes M, Shah P, Hussain K. Roženková K, et al. Among authors: hussain k. J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):86-97. doi: 10.4274/jcrpe.1891. J Clin Res Pediatr Endocrinol. 2015. PMID: 26316429 Free PMC article. Review.
Nifedipine in Congenital Hyperinsulinism - A Case Report.
Khawash P, Hussain K, Flanagan SE, Chatterjee S, Basak D. Khawash P, et al. Among authors: hussain k. J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):151-4. doi: 10.4274/jcrpe.1978. J Clin Res Pediatr Endocrinol. 2015. PMID: 26316440 Free PMC article.
A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus.
Ünal S, Gönülal D, Uçaktürk A, Siyah Bilgin B, Flanagan SE, Gürbüz F, Tayfun M, Elmaoğulları S, Araslı A, Demirel F, Ellard S, Hussain K. Ünal S, et al. Among authors: hussain k. J Clin Res Pediatr Endocrinol. 2016 Dec 1;8(4):478-481. doi: 10.4274/jcrpe.2773. Epub 2016 May 16. J Clin Res Pediatr Endocrinol. 2016. PMID: 27181099 Free PMC article.
952 results