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2005 1
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Page 1
Criteria for radiologic diagnosis of hypochondroplasia in neonates.
Saito T, Nagasaki K, Nishimura G, Wada M, Nyuzuki H, Takagi M, Hasegawa T, Amano N, Murotsuki J, Sawai H, Yamada T, Sato S, Saitoh A. Saito T, et al. Among authors: takagi m. Pediatr Radiol. 2016 Apr;46(4):513-8. doi: 10.1007/s00247-015-3518-2. Epub 2016 Feb 11. Pediatr Radiol. 2016. PMID: 26867606
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. Among authors: takagi m. 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
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.
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. 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
Two novel mutations of COMP in Japanese boys with pseudoachondroplasia.
Ichihashi Y, Takagi M, Ishii T, Watanabe K, Nishimura G, Hasegawa T. Ichihashi Y, et al. Among authors: takagi m. Hum Genome Var. 2018 Jun 8;5:12. doi: 10.1038/s41439-018-0012-z. eCollection 2018. Hum Genome Var. 2018. PMID: 29899997 Free PMC article.
56 results