Ida S - Search Results

1

Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature.

Hattori A, Katoh-Fukui Y, Nakamura A, Matsubara K, Kamimaki T, Tanaka H, Dateki S, Adachi M, Muroya K, Yoshida S, Ida S, Mitani M, Nagasaki K, Ogata T, Suzuki E, Hata K, Nakabayashi K, Matsubara Y, Narumi S, Tanaka T, Fukami M. Hattori A, et al. Among authors: ida s. Endocr J. 2017 Oct 28;64(10):947-954. doi: 10.1507/endocrj.EJ17-0150. Epub 2017 Aug 3. Endocr J. 2017. PMID: 28768959 Free article.

2

Resting energy expenditure in short-stature children.

Nishimoto Y, Ida S, Etani Y, Miyatani S. Nishimoto Y, et al. Among authors: ida s. Endocr J. 2012;59(3):265-71. doi: 10.1507/endocrj.ej11-0138. Epub 2012 Jan 7. Endocr J. 2012. PMID: 22230811 Free article.

3

Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.

Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T, Fukami M. Igarashi M, et al. Among authors: ida s. PLoS One. 2013 Jul 8;8(7):e68194. doi: 10.1371/journal.pone.0068194. Print 2013. PLoS One. 2013. PMID: 23861871 Free PMC article.

4

Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997-2017.

Matsushita R, Nagasaki K, Ayabe T, Miyoshi Y, Kinjo S, Haruna H, Ihara K, Hasegawa T, Ida S, Ozono K, Minamitani K; Thyroid Committee of the Japanese Society for Pediatric Endocrinology. Matsushita R, et al. Among authors: ida s. J Pediatr Endocrinol Metab. 2019 Jun 26;32(6):585-595. doi: 10.1515/jpem-2018-0444. J Pediatr Endocrinol Metab. 2019. PMID: 31150358 Free article.

5

Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.

Shoji Y, Ida S, Niihori T, Aoki Y, Okamoto N, Etani Y, Kawai M. Shoji Y, et al. Among authors: ida s. Endocr J. 2019 Nov 28;66(11):983-994. doi: 10.1507/endocrj.EJ18-0564. Epub 2019 Jul 10. Endocr J. 2019. PMID: 31292302 Free article.

6

MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene.

Onuma S, Wada T, Araki R, Wada K, Tanase-Nakao K, Narumi S, Fukui M, Shoji Y, Etani Y, Ida S, Kawai M. Onuma S, et al. Among authors: ida s. Hum Genome Var. 2020 Mar 5;7:4. doi: 10.1038/s41439-020-0091-5. eCollection 2020. Hum Genome Var. 2020. PMID: 32194975 Free PMC article.

7

Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis.

Koizumi M, Ida S, Shoji Y, Nishimoto Y, Etani Y, Kawai M. Koizumi M, et al. Among authors: ida s. Endocr J. 2020 Oct 28;67(10):1029-1037. doi: 10.1507/endocrj.EJ19-0489. Epub 2020 Jun 19. Endocr J. 2020. PMID: 32565499 Free article.

8

[No title available]

[No authors listed] [No authors listed] PMID: 33419973

9

Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists.

Takasawa K, Nakamura-Utsunomiya A, Amano N, Ishii T, Hasegawa T, Hasegawa Y, Tajima T, Ida S. Takasawa K, et al. Among authors: ida s. Endocr J. 2022 Jan 28;69(1):75-83. doi: 10.1507/endocrj.EJ21-0292. Epub 2021 Aug 7. Endocr J. 2022. PMID: 34373418 Free article.

10

Dosage of hydrocortisone during late infancy is positively associated with changes in body mass index during early childhood in patients with 21-hydroxylase deficiency.

Wada T, Nishigaki S, Hata A, Maeyama T, Ida S, Etani Y, Kawai M. Wada T, et al. Among authors: ida s. Endocr J. 2023 Mar 28;70(3):333-340. doi: 10.1507/endocrj.EJ22-0466. Epub 2022 Dec 10. Endocr J. 2023. PMID: 36504089 Free article.

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