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Heterozygous defects in PAX6 gene and congenital hypopituitarism.
Takagi M, Nagasaki K, Fujiwara I, Ishii T, Amano N, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T. Takagi M, et al. Among authors: amano n. Eur J Endocrinol. 2015 Jan;172(1):37-45. doi: 10.1530/EJE-14-0255. Epub 2014 Oct 23. Eur J Endocrinol. 2015. PMID: 25342853
Genetic defects in pediatric-onset adrenal insufficiency in Japan.
Amano N, Narumi S, Hayashi M, Takagi M, Imai K, Nakamura T, Hachiya R, Sasaki G, Homma K, Ishii T, Hasegawa T. Amano N, et al. Eur J Endocrinol. 2017 Aug;177(2):187-194. doi: 10.1530/EJE-17-0027. Epub 2017 May 25. Eur J Endocrinol. 2017. PMID: 28546232
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
Shima H, Hayashi M, Tachibana T, Oshiro M, Amano N, Ishii T, Haruna H, Igarashi M, Kon M, Fukuzawa R, Tanaka Y, Fukami M, Hasegawa T, Narumi S. Shima H, et al. Among authors: amano n. PLoS One. 2018 Nov 7;13(11):e0206184. doi: 10.1371/journal.pone.0206184. eCollection 2018. PLoS One. 2018. PMID: 30403727 Free PMC article.
Fibroblast growth factor 23 levels in cord and peripheral blood during early neonatal period as possible predictors of affected offspring of X-linked hypophosphatemic rickets: report of three female cases from two pedigrees.
Nabeshima Y, Sato T, Zukeran H, Komatsu R, Nakano S, Ichihashi Y, Tominaga T, Miwa M, Amano N, Ishii T, Hasegawa T. Nabeshima Y, et al. Among authors: amano n. J Pediatr Endocrinol Metab. 2023 Jun 22;36(8):786-790. doi: 10.1515/jpem-2023-0120. Print 2023 Aug 28. J Pediatr Endocrinol Metab. 2023. PMID: 37342899
404 results