Utari A - Search Results

1

Ten-Year Experience of a Global and Freely Accessible e-Learning Website for Pediatric Endocrinology and Diabetes.

Ng SM, Kalaitzoglou E, Utari A, van Wijngaard-de Vugt C, Donaldson M, Wolfsdorf JI, Boot AM, Drop S. Ng SM, et al. Among authors: utari a. Horm Res Paediatr. 2023;96(4):366-375. doi: 10.1159/000527984. Epub 2022 Nov 8. Horm Res Paediatr. 2023. PMID: 36349753 Free article.

2

Childhood Obesity as a Global Problem: a Cross-sectional Survey on Global Awareness and National Program Implementation.

Pulungan AB, Puteri HA, Ratnasari AF, Hoey H, Utari A, Darendeliler F, Al-Zoubi B, Joel D, Valiulis A, Cabana J, Hasanoğlu E, Thacker N, Farmer M. Pulungan AB, et al. Among authors: utari a. J Clin Res Pediatr Endocrinol. 2024 Mar 11;16(1):31-40. doi: 10.4274/jcrpe.galenos.2023.2023-7-5. Epub 2023 Aug 25. J Clin Res Pediatr Endocrinol. 2024. PMID: 37622285 Free PMC article.

3

Knowledge of genetics and attitudes toward genetic testing among university students in Indonesia.

Hermanto I, Chandra CK, Utari A, Winarni TI, Cayami FK. Hermanto I, et al. Among authors: utari a. J Community Genet. 2024 Aug;15(4):433-447. doi: 10.1007/s12687-024-00711-0. Epub 2024 Jun 8. J Community Genet. 2024. PMID: 38851656 Free PMC article.

4

Free cortisol and free 21-deoxycortisol in the clinical evaluation of congenital adrenal hyperplasia.

Adriaansen BPH, Utari A, Olthaar AJ, van der Steen RCBM, Pijnenburg-Kleizen KJ, Berkenbosch L, Span PN, Sweep FCGJ, Claahsen-van der Grinten HL, van Herwaarden AE. Adriaansen BPH, et al. Among authors: utari a. J Clin Endocrinol Metab. 2024 Aug 24:dgae591. doi: 10.1210/clinem/dgae591. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 39183148

5

46,XX males with congenital adrenal hyperplasia: a clinical and biochemical description.

Adriaansen BPH, Utari A, Westra D, Juniarto AZ, Ariani MD, Ediati A, Schröder MAM, Span PN, Sweep FCGJ, Drop SLS, Faradz SMH, van Herwaarden AE, Claahsen-van der Grinten HL. Adriaansen BPH, et al. Among authors: utari a. Front Endocrinol (Lausanne). 2024 Aug 8;15:1410122. doi: 10.3389/fendo.2024.1410122. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39175568 Free PMC article.

6

Early identification and treatment of genetic and neurodevelopmental disorders.

Winarni TI, Utari A, Maharani N, Sumekar TA, Sihombing NRB, Hagerman RJ. Winarni TI, et al. Among authors: utari a. J Intellect Disabil Res. 2024 Sep;68(9):1007-1009. doi: 10.1111/jir.13175. J Intellect Disabil Res. 2024. PMID: 39171562 No abstract available.

7

Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome.

Winarni TI, Hwang YH, Rivera SM, Hessl D, Durbin-Johnson BP, Utari A, Hagerman R, Tassone F. Winarni TI, et al. Among authors: utari a. Int J Mol Sci. 2024 Jul 25;25(15):8103. doi: 10.3390/ijms25158103. Int J Mol Sci. 2024. PMID: 39125677 Free PMC article.

8

Prevalence and factors associated with celiac disease in high-risk patients with functional gastrointestinal disorders.

Syam AF, Utari AP, Hasanah NH, Rizky A, Abdullah M. Syam AF, et al. Among authors: utari ap. PLoS One. 2024 Jun 7;19(6):e0297605. doi: 10.1371/journal.pone.0297605. eCollection 2024. PLoS One. 2024. PMID: 38848393 Free PMC article.

9

Critical issue in the identification of Down syndrome and its problems in Central Java, Indonesia: The fact of needing health care and better management.

Utari A, Cayami FK, Rahardjo TA, Sabatini SE, Ulvyana V, Winarni TI. Utari A, et al. Intractable Rare Dis Res. 2024 May 31;13(2):121-125. doi: 10.5582/irdr.2023.01103. Intractable Rare Dis Res. 2024. PMID: 38836178 Free PMC article.

10

Experiences and Challenges with Congenital Hypothyroidism Newborn Screening in Indonesia: A National Cross-Sectional Survey.

Pulungan AB, Puteri HA, Faizi M, Hofman PL, Utari A, Chanoine JP. Pulungan AB, et al. Among authors: utari a. Int J Neonatal Screen. 2024 Jan 19;10(1):8. doi: 10.3390/ijns10010008. Int J Neonatal Screen. 2024. PMID: 38390972 Free PMC article.

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