Yagi H - Search Results

1

Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD.

Hasegawa Y, Ariyasu D, Izawa M, Igaki-Miyamoto J, Fukuma M, Hatano M, Yagi H, Goto M. Hasegawa Y, et al. Among authors: yagi h. Endocr J. 2017 Feb 27;64(2):221-227. doi: 10.1507/endocrj.EJ16-0170. Epub 2016 Dec 2. Endocr J. 2017. PMID: 27916781 Free article.

2

Fertility preservation in a family with a novel NR5A1 mutation.

Yagi H, Takagi M, Kon M, Igarashi M, Fukami M, Hasegawa Y. Yagi H, et al. Endocr J. 2015;62(3):289-95. doi: 10.1507/endocrj.EJ14-0340. Epub 2014 Dec 12. Endocr J. 2015. PMID: 25502990 Free article.

3

Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset.

Fukuma M, Ariyasu D, Hatano M, Yagi H, Hasegawa Y. Fukuma M, et al. Among authors: yagi h. Clin Pediatr Endocrinol. 2016 Apr;25(2):67-9. doi: 10.1297/cpe.25.67. Epub 2016 Apr 28. Clin Pediatr Endocrinol. 2016. PMID: 27212798 Free PMC article. No abstract available.

4

Five cases of childhood-onset Graves' disease treated with either surgery or radio-iodine therapy.

Tomari K, Goto M, Shimada A, Yagi H, Nagashima Y, Hasegawa Y. Tomari K, et al. Among authors: yagi h. Clin Pediatr Endocrinol. 2017;26(4):265-269. doi: 10.1297/cpe.26.265. Epub 2017 Sep 28. Clin Pediatr Endocrinol. 2017. PMID: 29026276 Free PMC article.

5

A case of transient neonatal diabetes due to a novel mutation in ABCC8.

Takagi M, Takeda R, Yagi H, Ariyasu D, Fukuzawa R, Hasegawa T. Takagi M, et al. Among authors: yagi h. Clin Pediatr Endocrinol. 2016 Oct;25(4):139-141. doi: 10.1297/cpe.25.139. Epub 2016 Oct 18. Clin Pediatr Endocrinol. 2016. PMID: 27780984 Free PMC article. No abstract available.

6

A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in TRAPPC2.

Fukuma M, Takagi M, Shimazu T, Imamura H, Yagi H, Nishimura G, Hasegawa T. Fukuma M, et al. Among authors: yagi h. Clin Pediatr Endocrinol. 2018;27(3):193-196. doi: 10.1297/cpe.27.193. Epub 2018 Jul 31. Clin Pediatr Endocrinol. 2018. PMID: 30083037 Free PMC article. No abstract available.

7

Functional Characterization of c.870+3_6delGAGT Splice Site Mutation in NR5A1.

Takagi M, Nishina N, Yagi H, Hasegawa Y. Takagi M, et al. Among authors: yagi h. Horm Res Paediatr. 2016;85(1):65-8. doi: 10.1159/000440862. Epub 2015 Sep 26. Horm Res Paediatr. 2016. PMID: 26406169

8

Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger.

Yagi H, Takagi M, Hasegawa Y, Kayserili H, Nishimura G. Yagi H, et al. Pediatr Radiol. 2015 Jul;45(8):1239-43. doi: 10.1007/s00247-015-3292-1. Epub 2015 Apr 3. Pediatr Radiol. 2015. PMID: 25835322

9

Stippled calcification in an infant with a recurrent SRCAP gene mutation.

Yagi H, Takagi M, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y. Yagi H, et al. Am J Med Genet A. 2016 Apr;170A(4):1088-91. doi: 10.1002/ajmg.a.37516. Epub 2016 Jan 20. Am J Med Genet A. 2016. PMID: 26788936 No abstract available.

10

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: yagi h. 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.

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