Ono H - Search Results

1

Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency.

Ono H, Numakura C, Homma K, Hasegawa T, Tsutsumi S, Kato F, Fujisawa Y, Fukami M, Ogata T. Ono H, et al. J Steroid Biochem Mol Biol. 2018 Apr;178:177-184. doi: 10.1016/j.jsbmb.2017.12.008. Epub 2017 Dec 28. J Steroid Biochem Mol Biol. 2018. PMID: 29289577

2

Critical role of Yp inversion in PRKX/PRKY-mediated Xp;Yp translocation in a patient with 45,X testicular disorder of sex development.

Nakashima S, Watanabe Y, Okada J, Ono H, Nagata E, Fukami M, Ogata T. Nakashima S, et al. Among authors: ono h. Endocr J. 2013;60(12):1329-34. doi: 10.1507/endocrj.ej13-0334. Epub 2013 Oct 3. Endocr J. 2013. PMID: 24088663 Free article.

3

Combined steroidogenic characters of fetal adrenal and Leydig cells in childhood adrenocortical carcinoma.

Fujisawa Y, Sakaguchi K, Ono H, Yamaguchi R, Kato F, Kagami M, Fukami M, Ogata T. Fujisawa Y, et al. Among authors: ono h. J Steroid Biochem Mol Biol. 2016 May;159:86-93. doi: 10.1016/j.jsbmb.2016.02.031. Epub 2016 Mar 3. J Steroid Biochem Mol Biol. 2016. PMID: 26940356

4

Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses.

Ohishi A, Nishimura G, Kato F, Ono H, Maruwaka K, Ago M, Suzumura H, Hirose E, Uchida Y, Fukami M, Ogata T. Ohishi A, et al. Among authors: ono h. Am J Med Genet A. 2017 Jan;173(1):157-162. doi: 10.1002/ajmg.a.37992. Epub 2016 Sep 28. Am J Med Genet A. 2017. PMID: 27683237

5

Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene.

Ono H, Saitsu H, Horikawa R, Nakashima S, Ohkubo Y, Yanagi K, Nakabayashi K, Fukami M, Fujisawa Y, Ogata T. Ono H, et al. Sci Rep. 2018 Feb 2;8(1):2287. doi: 10.1038/s41598-018-20691-9. Sci Rep. 2018. PMID: 29396419 Free PMC article.

6

Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal Region.

Fukami M, Fujisawa Y, Ono H, Jinno T, Ogata T. Fukami M, et al. Among authors: ono h. Genome Biol Evol. 2020 Nov 3;12(11):1961-1964. doi: 10.1093/gbe/evaa168. Genome Biol Evol. 2020. PMID: 32785664 Free PMC article.

7

Insulin resistant diabetes mellitus in SHORT syndrome: case report and literature review.

Masunaga Y, Fujisawa Y, Muramatsu M, Ono H, Inoue T, Fukami M, Kagami M, Saitsu H, Ogata T. Masunaga Y, et al. Among authors: ono h. Endocr J. 2021 Jan 28;68(1):111-117. doi: 10.1507/endocrj.EJ20-0291. Epub 2020 Sep 3. Endocr J. 2021. PMID: 32879144 Free article. Review.

8

Case Report: Efficacy of Reduced Doses of Asfotase Alfa Replacement Therapy in an Infant With Hypophosphatasia Who Lacked Severe Clinical Symptoms.

Fujisawa Y, Kitaoka T, Ono H, Nakashima S, Ozono K, Ogata T. Fujisawa Y, et al. Among authors: ono h. Front Endocrinol (Lausanne). 2020 Dec 18;11:590455. doi: 10.3389/fendo.2020.590455. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 33391183 Free PMC article.

9

Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse.

Fujisawa Y, Ono H, Konno A, Yao I, Itoh H, Baba T, Morohashi K, Katoh-Fukui Y, Miyado M, Fukami M, Ogata T. Fujisawa Y, et al. Among authors: ono h. J Endocr Soc. 2022 Feb 15;6(4):bvac022. doi: 10.1210/jendso/bvac022. eCollection 2022 Apr 1. J Endocr Soc. 2022. PMID: 35265782 Free PMC article.

10

Sotos syndrome with marked overgrowth in three Japanese patients with heterozygous likely pathogenic NSD1 variants: case reports with review of literature.

Masunaga Y, Ono H, Fujisawa Y, Taniguchi K, Saitsu H, Ogata T. Masunaga Y, et al. Among authors: ono h. Endocr J. 2024 Jan 29;71(1):75-81. doi: 10.1507/endocrj.EJ23-0502. Epub 2023 Nov 22. Endocr J. 2024. PMID: 37989294 Free article. Review.

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