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We All Have a Role to Play: Redressing Inequities for Children Living with CAH and Other Chronic Health Conditions of Childhood in Resource-Poor Settings.
Armstrong K, Benedict Yap A, Chan-Cua S, Craig ME, Cole C, Chi Dung V, Hansen J, Ibrahim M, Nadeem H, Pulungan A, Raza J, Utari A, Ward P. Armstrong K, et al. Among authors: utari a. Int J Neonatal Screen. 2020 Sep 25;6(4):76. doi: 10.3390/ijns6040076. Int J Neonatal Screen. 2020. PMID: 33124614 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.
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.
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.
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