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Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals.
Sihombing NRB, Cai S, Wong DPW, Guan M, Chong SS, Faradz SMH, Winarni TI. Sihombing NRB, et al. Among authors: faradz smh. Singapore Med J. 2021 Mar;62(3):143-148. doi: 10.11622/smedj.2020009. Epub 2020 Jan 28. Singapore Med J. 2021. PMID: 31989181 Free PMC article.
Corrigendum: 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. Among authors: faradz smh. Front Endocrinol (Lausanne). 2023 May 4;14:1210892. doi: 10.3389/fendo.2023.1210892. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37214254 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. Among authors: faradz smh. 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: faradz smh. 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.
70 results