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Year Number of Results
2009 1
2010 2
2011 1
2012 1
2013 1
2016 1
2018 2
2019 3
2020 2
2021 4
2022 4
2023 6
2024 2

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Page 1
Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
Claahsen-van der Grinten HL, Speiser PW, Ahmed SF, Arlt W, Auchus RJ, Falhammar H, Flück CE, Guasti L, Huebner A, Kortmann BBM, Krone N, Merke DP, Miller WL, Nordenström A, Reisch N, Sandberg DE, Stikkelbroeck NMML, Touraine P, Utari A, Wudy SA, White PC. Claahsen-van der Grinten HL, et al. Among authors: utari a. Endocr Rev. 2022 Jan 12;43(1):91-159. doi: 10.1210/endrev/bnab016. Endocr Rev. 2022. PMID: 33961029 Free PMC article. Review.
Sociocultural aspects of disorders of sex development.
Ediati A, Maharani N, Utari A. Ediati A, et al. Among authors: utari a. Birth Defects Res C Embryo Today. 2016 Dec;108(4):380-383. doi: 10.1002/bdrc.21144. Birth Defects Res C Embryo Today. 2016. PMID: 28033662 Review.
Turner syndrome in diverse populations.
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong MK, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, de Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Kruszka P, et al. Among authors: utari a. Am J Med Genet A. 2020 Feb;182(2):303-313. doi: 10.1002/ajmg.a.61461. Epub 2019 Dec 19. Am J Med Genet A. 2020. PMID: 31854143 Free PMC article.
Surveillance and prevalence of fragile X syndrome in Indonesia.
Sihombing NRB, Winarni TI, Utari A, van Bokhoven H, Hagerman RJ, Faradz SM. Sihombing NRB, et al. Among authors: utari a. Intractable Rare Dis Res. 2021 Feb;10(1):11-16. doi: 10.5582/irdr.2020.03101. Intractable Rare Dis Res. 2021. PMID: 33614370 Free PMC article. Review.
Aging in fragile X syndrome.
Utari A, Adams E, Berry-Kravis E, Chavez A, Scaggs F, Ngotran L, Boyd A, Hessl D, Gane LW, Tassone F, Tartaglia N, Leehey MA, Hagerman RJ. Utari A, et al. J Neurodev Disord. 2010 Jun;2(2):70-76. doi: 10.1007/s11689-010-9047-2. Epub 2010 May 12. J Neurodev Disord. 2010. PMID: 20585378 Free PMC article.
Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries.
Waaijers S, Utari A, van der Doelen RHA, Faradz SMH, Hensen-Lodewijk R, Olthaar AJ, Geutjes PJ, Sweep FC, Claahsen-van der Grinten HL, van Herwaarden AE. Waaijers S, et al. Among authors: utari a. Clin Endocrinol (Oxf). 2023 Jan;98(1):41-48. doi: 10.1111/cen.14754. Epub 2022 May 15. Clin Endocrinol (Oxf). 2023. PMID: 35514026 Free PMC article.
Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country.
Utari A, Faradz SMH, Ediati A, Rinne T, Ariani MD, Juniarto AZ, Drop SLS, van Herwaarden AE, Claahsen-van der Grinten HL. Utari A, et al. Front Endocrinol (Lausanne). 2022 Dec 15;13:1015973. doi: 10.3389/fendo.2022.1015973. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36589846 Free PMC article.
25 results