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Congenital adrenal hyperplasia and the second newborn screen.
Chan CL, McFann K, Taylor L, Wright D, Zeitler PS, Barker JM. Chan CL, et al. Among authors: barker jm. J Pediatr. 2013 Jul;163(1):109-13.e1. doi: 10.1016/j.jpeds.2013.01.002. Epub 2013 Feb 12. J Pediatr. 2013. PMID: 23414665
Case report: an 11-year-old girl with tetany.
Barker J, Travers S. Barker J, et al. Curr Opin Pediatr. 2002 Jun;14(3):338-42. doi: 10.1097/00008480-200206000-00011. Curr Opin Pediatr. 2002. PMID: 12011676 No abstract available.
Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes.
Triolo TM, Baschal EE, Armstrong TK, Toews CS, Fain PR, Rewers MJ, Yu L, Miao D, Eisenbarth GS, Gottlieb PA, Barker JM. Triolo TM, et al. Among authors: barker jm. J Clin Endocrinol Metab. 2009 Nov;94(11):4517-23. doi: 10.1210/jc.2009-1308. Epub 2009 Oct 9. J Clin Endocrinol Metab. 2009. PMID: 19820007 Free PMC article.
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