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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. Among authors: nagasaka h. 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
Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.
Yorifuji T, Matsubara K, Sakakibara A, Hashimoto Y, Kawakita R, Hosokawa Y, Fujimaru R, Murakami A, Tamagawa N, Hatake K, Nagasaka H, Suzuki J, Urakami T, Izawa M, Kagami M. Yorifuji T, et al. Among authors: nagasaka h. Diabet Med. 2015 Jul;32(7):963-7. doi: 10.1111/dme.12758. Epub 2015 Apr 11. Diabet Med. 2015. PMID: 25809823
Genetic basis of early-onset, maturity-onset diabetes of the young-like diabetes in Japan and features of patients without mutations in the major MODY genes: Dominance of maternal inheritance.
Yorifuji T, Higuchi S, Kawakita R, Hosokawa Y, Aoyama T, Murakami A, Kawae Y, Hatake K, Nagasaka H, Tamagawa N. Yorifuji T, et al. Among authors: nagasaka h. Pediatr Diabetes. 2018 Nov;19(7):1164-1172. doi: 10.1111/pedi.12714. Epub 2018 Jul 1. Pediatr Diabetes. 2018. PMID: 29927023
239 results