Grover G, Jahagirdar R, Deshpande R, Shinde M
Cureus. 2025; 16(12):e76218.
PMID: 39845257
PMC: 11753809.
DOI: 10.7759/cureus.76218.
Yavas Abali Z, Kurnaz E, Guran T
J Clin Res Pediatr Endocrinol. 2024; 17(Suppl 1):33-43.
PMID: 39713885
PMC: 11730100.
DOI: 10.4274/jcrpe.galenos.2024.2024-6-10-S.
Chandran J, Bellad A, Ramarajan M, Rangiah K
Anal Sci Adv. 2024; 2(11-12):546-563.
PMID: 38715861
PMC: 10989570.
DOI: 10.1002/ansa.202100010.
Castro S, Wiest P, Spritzer P, Kopacek C
Endocr Connect. 2023; 12(12).
PMID: 37902057
PMC: 10620452.
DOI: 10.1530/EC-23-0162.
de Hora M, Heather N, Webster D, Albert B, Hofman P
Front Endocrinol (Lausanne). 2023; 14:1226284.
PMID: 37850096
PMC: 10578435.
DOI: 10.3389/fendo.2023.1226284.
The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD): I) Physiology, classification, approach, and methodologyII) Biochemical and genetic markers in 46,XX DSD.
Granada M, Audi L
Adv Lab Med. 2023; 2(4):468-493.
PMID: 37360895
PMC: 10197333.
DOI: 10.1515/almed-2021-0042.
Multiple 17-OHP Cutoff Co-Variates Fail to Improve 21-Hydroxylase Deficiency Screening Accuracy.
Matharu P, Held P, Allen D
Int J Neonatal Screen. 2022; 8(4).
PMID: 36412583
PMC: 9680344.
DOI: 10.3390/ijns8040057.
Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision).
Ishii T, Kashimada K, Amano N, Takasawa K, Nakamura-Utsunomiya A, Yatsuga S
Clin Pediatr Endocrinol. 2022; 31(3):116-143.
PMID: 35928387
PMC: 9297175.
DOI: 10.1297/cpe.2022-0009.
Moderate congenital adrenal hyperplasia in two girls diagnosed by newborn screening.
Banaszak-Ziemska M, Malecka E, Lacna K, Ginalska-Malinowska M, Niedziela M
Pediatr Endocrinol Diabetes Metab. 2022; 27(4):291-297.
PMID: 35114771
PMC: 10226346.
DOI: 10.5114/pedm.2021.109123.
Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan.
Tsuji-Hosokawa A, Kashimada K
Int J Neonatal Screen. 2021; 7(3).
PMID: 34209888
PMC: 8293132.
DOI: 10.3390/ijns7030036.
Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
Claahsen-van der Grinten H, Speiser P, Ahmed S, Arlt W, Auchus R, Falhammar H
Endocr Rev. 2021; 43(1):91-159.
PMID: 33961029
PMC: 8755999.
DOI: 10.1210/endrev/bnab016.
Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population.
Wang X, Wang Y, Ma D, Zhang Z, Li Y, Yang P
Front Genet. 2021; 11:623125.
PMID: 33552137
PMC: 7862715.
DOI: 10.3389/fgene.2020.623125.
[Analysis of the degree of clinical suspect in patients with congenital adrenal hyperplasia by 21-hydroxylase deficiency before obtaining the result of the newborn screening program of the autonomous Community of Madrid.].
Sanz Fernandez M, Mora Sitja M, Carrascon Gonzalez Pinto L, Rodriguez Sanchez A
Rev Esp Salud Publica. 2020; 94.
PMID: 33372915
PMC: 11582765.
Update on the Swedish Newborn Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Zetterstrom R, Karlsson L, Falhammar H, Lajic S, Nordenstrom A
Int J Neonatal Screen. 2020; 6(3).
PMID: 33239597
PMC: 7570065.
DOI: 10.3390/ijns6030071.
Landscape of Congenital Adrenal Hyperplasia Newborn Screening in the United States.
Edelman S, Desai H, Pigg T, Yusuf C, Ojodu J
Int J Neonatal Screen. 2020; 6(3).
PMID: 33239590
PMC: 7569894.
DOI: 10.3390/ijns6030064.
Newborn Screening for Congenital Adrenal Hyperplasia: Review of Factors Affecting Screening Accuracy.
Held P, Bird I, Heather N
Int J Neonatal Screen. 2020; 6(3):67.
PMID: 33117906
PMC: 7569755.
DOI: 10.3390/ijns6030067.
Evaluation of a Two-Tier Screening Pathway for Congenital Adrenal Hyperplasia in the New South Wales Newborn Screening Programme.
Lai F, Srinivasan S, Wiley V
Int J Neonatal Screen. 2020; 6(3):63.
PMID: 33117905
PMC: 7569785.
DOI: 10.3390/ijns6030063.
Wisconsin's Screening Algorithm for the Identification of Newborns with Congenital Adrenal Hyperplasia.
Bialk E, Lasarev M, Held P
Int J Neonatal Screen. 2020; 5(3):33.
PMID: 33072992
PMC: 7510207.
DOI: 10.3390/ijns5030033.
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.
Speiser P, Arlt W, Auchus R, Baskin L, Conway G, Merke D
J Clin Endocrinol Metab. 2018; 103(11):4043-4088.
PMID: 30272171
PMC: 6456929.
DOI: 10.1210/jc.2018-01865.
17-hydroxiprogesterone values in healthy preterm infants.
Mendoza-Rojas V, Diaz-Martinez L, Mantilla-Mora G, Contreras-Garcia G, Mora-Bautista V, Martinez-Paredes J
Colomb Med (Cali). 2018; 48(4):161-166.
PMID: 29662257
PMC: 5896722.
DOI: 10.25100/cm.v43i4.2983.