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Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.
Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, Nomura A, Masue M, Nishibori H, Yoshizawa A, Okamoto S, Doi R, Uemoto S, Nagasaka H. Yorifuji T, et al. J Clin Endocrinol Metab. 2011 Jan;96(1):E141-5. doi: 10.1210/jc.2010-1281. Epub 2010 Oct 13. J Clin Endocrinol Metab. 2011. PMID: 20943781
Diabetes caused by Kir6.2 mutation: successful treatment with oral glibenclamide switched from continuous subcutaneous insulin infusion in the early phase of the disease.
Nagano N, Urakami T, Mine Y, Watanabe H, Yoshida A, Suzuki J, Saito H, Ishige M, Takahashi S, Mugishima H, Yorifuji T. Nagano N, et al. Among authors: yorifuji t. Pediatr Int. 2012 Apr;54(2):277-9. doi: 10.1111/j.1442-200X.2011.03413.x. Pediatr Int. 2012. PMID: 22507152 No abstract available.
484 results