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Page 1
A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3.
Nagahara K, Harada Y, Futami T, Takagi M, Nishimura G, Hasegawa Y. Nagahara K, et al. Among authors: takagi m. Clin Pediatr Endocrinol. 2016 Jul;25(3):103-6. doi: 10.1297/cpe.25.103. Epub 2016 Jul 20. Clin Pediatr Endocrinol. 2016. PMID: 27507911 Free PMC article. No abstract available.
A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide.
Takeda R, Takagi M, Miyai K, Shinohara H, Yagi H, Moritani M, Yokota I, Hasegawa Y. Takeda R, et al. Among authors: takagi m. Clin Pediatr Endocrinol. 2015 Oct;24(4):191-3. doi: 10.1297/cpe.24.191. Epub 2015 Oct 24. Clin Pediatr Endocrinol. 2015. PMID: 26568660 Free PMC article. No abstract available.
3,068 results