Amano N - Search Results

1

Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study.

Hosokawa M, Ichihashi Y, Sato Y, Shibata N, Nagasaki K, Ikegawa K, Hasegawa Y, Hamajima T, Nagamatsu F, Suzuki S, Numakura C, Amano N, Sasaki G, Nagahara K, Soneda S, Ariyasu D, Maeda M, Kamasaki H, Aso K, Hasegawa T, Ishii T. Hosokawa M, et al. Among authors: amano n. J Clin Endocrinol Metab. 2024 Jul 12;109(8):e1602-e1607. doi: 10.1210/clinem/dgad753. J Clin Endocrinol Metab. 2024. PMID: 38128002

2

Radiological evolution in IMAGe association: a case report.

Amano N, Naoaki H, Ishii T, Narumi S, Hachiya R, Nishimura G, Hasegawa T. Amano N, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2130-3. doi: 10.1002/ajmg.a.32425. Am J Med Genet A. 2008. PMID: 18627061

3

The effect of intramuscular testosterone enanthate treatment on stretched penile length in prepubertal boys with hypospadias.

Ishii T, Hayashi M, Suwanai A, Amano N, Hasegawa T. Ishii T, et al. Among authors: amano n. Urology. 2010 Jul;76(1):97-100. doi: 10.1016/j.urology.2009.12.065. Epub 2010 Mar 28. Urology. 2010. PMID: 20350750

4

A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta.

Takagi M, Ishii T, Barnes AM, Weis M, Amano N, Tanaka M, Fukuzawa R, Nishimura G, Eyre DR, Marini JC, Hasegawa T. Takagi M, et al. Among authors: amano n. PLoS One. 2012;7(5):e36809. doi: 10.1371/journal.pone.0036809. Epub 2012 May 15. PLoS One. 2012. PMID: 22615817 Free PMC article.

5

Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.

Takagi M, Ishii T, Inokuchi M, Amano N, Narumi S, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T. Takagi M, et al. Among authors: amano n. PLoS One. 2012;7(9):e46008. doi: 10.1371/journal.pone.0046008. Epub 2012 Sep 24. PLoS One. 2012. PMID: 23029363 Free PMC article.

6

IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients.

Kato F, Hamajima T, Hasegawa T, Amano N, Horikawa R, Nishimura G, Nakashima S, Fuke T, Sano S, Fukami M, Ogata T. Kato F, et al. Among authors: amano n. Clin Endocrinol (Oxf). 2014 May;80(5):706-13. doi: 10.1111/cen.12379. Epub 2013 Dec 28. Clin Endocrinol (Oxf). 2014. PMID: 24313804

7

Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature.

Amano N, Mukai T, Ito Y, Narumi S, Tanaka T, Yokoya S, Ogata T, Hasegawa T. Amano N, et al. J Clin Endocrinol Metab. 2014 Apr;99(4):E713-8. doi: 10.1210/jc.2013-3525. Epub 2014 Jan 28. J Clin Endocrinol Metab. 2014. PMID: 24471569

8

A novel mutation of androgen receptor gene in complete androgen insensitivity syndrome.

Narumi S, Amano N, Hachiya R, Ishii T, Hasegawa T. Narumi S, et al. Among authors: amano n. Clin Pediatr Endocrinol. 2007;16(2):59-61. doi: 10.1297/cpe.16.59. Epub 2007 May 17. Clin Pediatr Endocrinol. 2007. PMID: 24790346 Free PMC article. No abstract available.

9

Growth failure in an infant with congenital nephrogenic diabetes insipidus during sodium restriction.

Sasaki G, Ishii T, Amano N, Hachiya R, Narumi S, Hasegawa T. Sasaki G, et al. Among authors: amano n. Clin Pediatr Endocrinol. 2007;16(4):95-8. doi: 10.1297/cpe.16.95. Epub 2007 Nov 17. Clin Pediatr Endocrinol. 2007. PMID: 24790353 Free PMC article.

10

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

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