Cited by 181Sexual Differentiation and DisordersAdrenal Hormones and DisordersHormonal Regulation and Hypertension

The DOI matches its Crossref record; 146 of the 155 references it cites were found in a registry or an index.

Adrenal Steroidogenesis and Congenital Adrenal Hyperplasia

Open access

Turcu, Adina F., Auchus, Richard J.·2015·Endocrinology and Metabolism Clinics of North America

DOI 10.1016/j.ecl.2015.02.002PMC PMC4506691

Open this paper in CoChat — free account

Abstract

Adrenal steroidogenesis is a dynamic process, reliant on de novo synthesis from cholesterol, under the stimulation of ACTH and other regulators. The syntheses of mineralocorticoids (primarily aldosterone), glucocorticoids (primarily cortisol), and adrenal androgens (primarily dehydroepiandrosterone and its sulfate) occur in separate adrenal cortical zones, each expressing specific enzymes. Congenital adrenal hyperplasia (CAH) encompasses a group of autosomal-recessive enzymatic defects in cortisol biosynthesis. 21-Hydroxylase (21OHD) deficiency accounts for more than 90% of CAH cases and, when milder or nonclassic forms are included, 21OHD is one of the most common genetic diseases.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1016/j.ecl.2015.02.002

Cites

146 of 146 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The Diagnosis of Polycystic Ovary Syndrome during Adolescence
Witchel, S. F., Oberfield, S., Rosenfield, R. L., Codner, E., Bonny, A., Ibáñez, L., Pena, A., Horikawa, R., Gomez-Lobo, V., Joel, D., et al. (2015) · Hormone Research in Paediatrics · doi:10.1159/000375530 · Cited by 3,113
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
Miller, W. L., & Auchus, R. J. (2011) · Endocrine Reviews · doi:10.1210/er.2010-0013 · Cited by 2,458
Self-citation
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society Clinical Practice Guideline.
Speiser, P. W., Azziz, R., Baskin, L. S., Ghizzoni, L., Hensle, T. W., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Montori, V. M., Oberfield, S. E., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-2631 · Cited by 1,468 · cited 5×
“If elected, treatment from an experienced team in research centers that monitor outcomes is recommended.(29)”
BackgroundInfluential
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency*
White, P. C., & Speiser, P. W. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.3.0398 · Cited by 1,432
Congenital Adrenal Hyperplasia
Speiser, P., & White, P. C. (1987) · New England Journal of Medicine · doi:10.1056/nejm198711263172211 · Cited by 1,420
Congenital adrenal hyperplasia
Speiser, P. W., & White, P. C. (2003) · New England Journal of Medicine · doi:10.1056/nejmra021561 · Cited by 1,405
The purification, cloning and expression of a novel luteinizing hormone-induced mitochondrial protein in MA-10 mouse Leydig tumor cells. Characterization of the steroidogenic acute regulatory protein (StAR)
Clark, B. J., Wells, J., King, S. R., & Stocco, D. M. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)46930-x · Cited by 1,168
Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
White, P. C. (2000) · Endocrine Reviews · doi:10.1210/er.21.3.245 · Cited by 877
The pathophysiology and genetics of congenital lipoid adrenal hyperplasia
Bose, H. S., Sugawara, T., Strauss, J. F., & Miller, W. L. (1996) · New England Journal of Medicine · doi:10.1056/nejm199612193352503 · Cited by 676
Genotyping steroid 21-hydroxylase deficiency: hormonal reference data
NEW, M. I., LORENZEN, F., LERNER, A. J., KOHN, B., OBERFIELD, S. E., POLLACK, M. S., DUPONT, B., STONER, E., LEVY, D. J., PANG, S., et al. (1983) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-57-2-320 · Cited by 624

Flagged first, then by citations

Show all 155 references

9 of the 155 references couldn’t be matched to a known paper.

Sorted by citations

Items 101–181 of 181

Clémentine Delait (1865–1934), the most famous bearded lady on the continent in the 20th century
de Herder, W. W. (2019) · Gynecological Endocrinology · doi:10.1080/09513590.2019.1683823 · Cited by 3
Beyond Binary: Gender Reassignment in a Case of 11β-Hydroxylase Deficiency
Hithayathulla, M. A., Nagarajan, H. D. P., Gopalakrishnan, V., Rishi, K. P., & Chandrasekaran, G. (2023) · Cureus · doi:10.7759/cureus.48644 · Cited by 3
Pubertad precoz por hiperplasia adrenal congénita. Reporte de caso
Dallos-Lara, M. F., & Mendoza-Rojas, V. C. (2020) · Revista de la Facultad de Medicina · doi:10.15446/revfacmed.v68n1.72674 · Cited by 3
A Broken Pathway: Understanding Congenital Adrenal Hyperplasia in the Newborn
Allis, K. (2021) · Neonatal Network The Journal of Neonatal Nursing · doi:10.1891/11-t-694 · Cited by 3
Lower birthweight and left‐/mixed‐handedness are associated with intensified age‐related sex steroid decline in men. Findings from the Men's Health 40+ Study
Hoppler, S., Walther, A., Ghaemmaghami, P., & Ehlert, U. (2018) · Andrology · doi:10.1111/andr.12516 · Cited by 3
Congenital adrenal hyperplasia complicated by gonadotropin-dependent precocious puberty
Alam, A., Agrawal, N. K., & Singh, S. K. (2024) · BMJ Case Reports · doi:10.1136/bcr-2023-257579 · Cited by 2
Enhancing Accuracy of Newborn Screening for 21OHD: Strategic Use of 21-Deoxycortisol in a Large-Scale Tokyo Cohort
Yamano, H., Watanabe, K., Komatsu, M., Hashimoto, A., Suzuki, Y. Y., Kirino, S., Saito, Y., Adachi, E., Gau, M., Nakatani, H., et al. (2025) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaf506 · Cited by 2
Untargeted metabolomics reveals distinct biomarkers and metabolic alterations in familial and non-genetic hypercholesterolemia in Saudi patients
Mahdi, H. B. A., Shaik, N. A., Awan, Z. A., Daghistani, H., Alandejani, F., Alghamdi, K. S., Obaid, A. A., Zahed, R., Hassan, R. N., Edris, S., et al. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1670282 · Cited by 2
Liquid chromatography-tandem mass spectrometry-based urinary steroid profiling applied to primary aldosteronism diagnosis
Zhong, J., Ma, X., Wang, D. X., Luo, W., Yin, Y., Zou, Y., Zhu, Y., Li, M., Xie, S., Ss, Y., et al. (2026) · Journal of Chromatography B · doi:10.1016/j.jchromb.2026.124930 · Cited by 2
Regulation of Adrenal Steroidogenesis
Pihlajoki, M., Heikinheimo, M., & Wilson, D. B. (2017) · Contemporary Endocrinology · doi:10.1007/978-3-319-62470-9_2 · Cited by 3
Résistances aux hormones stéroïdes : physiologie et pathologie
Ramos, N., & Lombès, M. (2016) · Annales d Endocrinologie · doi:10.1016/s0003-4266(17)30072-0 · Cited by 2
Rare nonclassic type of Congenital adrenal hyperplasia due to 21-hydroxylase deficiency and genotype-phenotypic correlation
Hou, Y., Li, Y., Ai, J., & Tian, L. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e27042 · Cited by 2
A comparison of obstetric and neonatal outcomes in polycystic ovary syndrome and congenital adrenal hyperplasia: a retrospective analysis of a population database
Kolokythas, A., Badeghiesh, A. M., Baghlaf, H. A., & Dahan, M. H. (2024) · F&S Science · doi:10.1016/j.xfss.2024.05.001 · Cited by 2
Successful Treatment Outcome in a Woman with Congenital Adrenal Hyperplasia
Shenoy, S. T., & Gopishyam, M. (2018) · The Journal of Obstetrics and Gynecology of India · doi:10.1007/s13224-018-1193-6 · Cited by 2
Dexamethasone affects human fetal adrenal steroidogenesis and subsequent ACTH response in an ex vivo culture model
Melau, C., Gayete-Mor, B., Riis, M. L., Nielsen, J. E., Dreisler, E., Aaboe, K., Brenøe, P. T., Thuesen, L. L., Hare, K. J., Mitchell, R. T., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1114211 · Cited by 2
Long-read sequencing resolves the clinically relevant CYP21A2 locus, supporting a new clinical test for Congenital Adrenal HyperplasiaPreprint
Monlong, J., Chen, X., Barseghyan, H., Rowell, W. J., Negi, S., Nokoff, N., Mohnach, L. H., Hirsch, J. A., Finlayson, C. A., Keegan, C. E., et al. (2025) · medRxiv · doi:10.1101/2025.02.07.25321404 · Cited by 2
Konjenital Adrenal Hiperplazi Vakalarında CYP21A2 Geni Kopya Sayısı Değişimlerinin MLPA Tekniği İle İncelenmesi
Mammadov, B., Yiğin, A. K., Özdemir, F., Özaydın, A., & Seven, M. (2020) · Phoenix Medical Journal · doi:10.38175/phnx.690298 · Cited by 1
Congenital Adrenal Hyperplasia: A Clinical Review
Harris, D. E. (2025) · Universal Library of Clinical Nursing · doi:10.70315/uloap.ulcnu.2025.0201002 · Cited by 1
Machine learning algorithms to accelerate etiological diagnosis of congenital disorders of adrenal steroidogenesis
Tosun, B. G., Erçetin, A. N., Turan, S., Bereket, A., Arğa, K. Y., & Güran, T. (2026) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgag237 · Cited by 1
Optimizing glucocorticoid therapy in congenital adrenal hyperplasia and analog conditions: the intersection of dose reduction, patient care, and coverage in the US
Khattab, A., Kim, H., Mulrooney, M., Leinwand, B., Hadker, N., Cicero, S., & Cheng, H. K.-H. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1603701 · Cited by 1
Transcript Patterns of Bovine CYP21A2 and Its Pseudogene in Adrenal and Ovarian Tissues
Wozniak, J., Stachowiak, M., Switonski, M., & Nowacka‐Woszuk, J. (2025) · Genes · doi:10.3390/genes16111374 · Cited by 1
Clinical practice guidelines "Congenital adrenal hyperplasia in children" with comments
Чугунов, І., Kopylova, I., Kolodkina, A. A., Kalinchenko, N. Y., Vorontsova, M. V., Bezlepkina, O. B., Peterkova, V. A., & Mokrysheva, N. G. (2026) · Problems of Endocrinology · doi:10.14341/probl13767 · Cited by 1
Inherited Metabolic Disorders: A Current Status
Shahid, M., Rasool, A., & Anjum, F. (2020) · Emerging contaminants and associated treatment technologies · doi:10.1007/978-3-030-45923-9_4 · Cited by 1
Síndrome de Cushing: uma revisão narrativa
Crespo, L. R., Velasco, L. D. A., Peres, D. T., Neto, M. D. L., & Teixeira, A. N. (2021) · Revista Científica da Faculdade de Medicina de Campos · doi:10.29184/1980-7813.rcfmc.495.vol.16.n1.2021 · Cited by 1
Improving Women's Health and Immunity: A Thorough Mapping Micronutrients and Dietary Recommendations
Pal, R. S., Pal, Y., Chaitanya, M., Sharma, N., Rani, A., Kumar, S., & Srivastava, P. (2024) · Current Drug Therapy · doi:10.2174/0115748855284781240202054050 · Cited by 1
Some Neonates with Congenital Adrenal Hyperplasia may Need Disproportionately High Doses of Mineralocorticoids
Pratasevich, T. S., Zhemoytiak, V. A., Denisik, N. I., Thenabadu, H. P., Hajzab, A. R. M., Lakmini, R. A. S., Perera, M. S. S., Matsiuk, I. N., & Thathsarani, S. H. C. H. (2025) · Newborn · doi:10.5005/jp-journals-11002-0128 · Cited by 1
A woman with primary amenorrhea due to non-Classical congenital adrenal hyperplasia
Bayu Aji, H., & Novida, H. (2025) · Perinatal Journal · doi:10.57239/prn.25.03320027 · Cited by 1
High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency
Kawasaki, Y., Sato, T., Nakano, S., Usui, T., Narumi, S., Ishii, T., & Hasegawa, T. (2022) · Clinical Pediatric Endocrinology · doi:10.1297/cpe.2021-0066 · Cited by 1
Adrenal Disorders
Scheckel, K. A. (2016) · Physician Assistant Clinics · doi:10.1016/j.cpha.2016.08.010
Application of Pharmacometrics to Rare Diseases
AHMED, M. A. (2016) · University of Minnesota Digital Conservancy (University of Minnesota)
Aplicação da cromatografia a gás associada à espectrometria de massas em tandem no diagnóstico da deficiência de 3β-hidroxidesidrogenase
Presutti, T. R. (2017) · doi:10.11606/d.9.2017.tde-10052017-152745
Effect of fish oil or algae meal supplementation on fetal and neonatal endotoxin-induced stress response
You, L. (2018) · The Atrium (University of Guelph)
CONGENITAL ADRENAL HYPERPLASIA: PRESENTING WITHHYPOCORTISOLISM; SEVEREHYPOCALCAEMIA; HYPOKALAEMIA AND HYPOGONADOTROPIC HYPOGONADISM.
IJAR, Sk, S., & Manghani, R. (2018) · International Journal of Advanced Research · doi:10.21474/ijar01/6800
Manejo con cinco antihipertensivos en paciente con pubertad precoz. Reporte de caso
de Santander, U. I., Ruiz-Rivera, M., Mendoza-Rojas, V. C., & de Santander, U. I. (2018) · IATREIA · doi:10.17533/udea.iatreia.v31n3a09
Deficiencia de 3β-hidroxiesteroide deshidrogenasa: una causa rara de hiperplasia adrenal congénita
González-Patiño, A., Monroy-Espejo, J., Toro-Ramos, M., Campuzano‐Maya, G., & Pineda-Trujillo, N. (2016) · Medicina y Laboratorio · doi:10.36384/01232576.84
Preputial Hood Anomalies
Fahmy, M. (2020) · Springer eBooks · doi:10.1007/978-3-030-37621-5_34
21-hydroxylase deficiency and fertility
Amiraslanova, M. M., & Kuznetsova, I. V. (2020) · Medical alphabet · doi:10.33667/2078-5631-2020-4-16-26
Nationellt miljökvalitetsmål på lokal nivå
Engkvist, F. (2011)
Congenital Adrenal Hyperplasia (CAH)
Al-Salem, A. H. (2020) · Springer eBooks · doi:10.1007/978-3-030-49984-6_20
The role of Aldosterone and PTH in Human Primary Aldosteronism and Vascular Calcification
Prisco, S. (2020) · doi:10.26481/dis.20201008sp
Adrenal Glands
Lack, E. E., & Paal, E. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-54941-7.00016-5
Premature Pubarche
Sultan, C., Gaspari, L., Kalfa, N., & Paris, F. (2017) · ISGE series · doi:10.1007/978-3-319-41433-1_5
Psychopharmacology of Sex Steroids
Swann, J. M., & Leung, C. H. (2019) · Springer eBooks · doi:10.1007/978-3-319-47829-6_634-1
21-Hydroxylase Deficiency: Clinical and Biochemical Aspects
Nordenström, A., & Lajić, S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65208-x
Apilot study Impact of glucocorticoid receptor gene polymorphism on the metabolic profile of child patients with classical form of 21-hydroxylase deficiency
ali, K., Shokeir, M., & Salem, N. A. (2022) · Mansoura Medical Journal · doi:10.21608/mjmu.2022.126765.1057
Hiperplasia adrenal congénita asociada a mutación no descrita en el gen CYP17A1
Builes-Montaño, C. E., Rueda-Galvis, M. V., Fragozo-Ramos, M. C., Agredo-Delgado, V., Lopera, J. Z., & Peña, C. M. M. (2022) · Revista Colombiana de Endocrinología Diabetes & Metabolismo · doi:10.53853/encr.9.2.750
Psychopharmacology of Sex Steroids
Swann, J. M., & Leung, C. H. (2022) · Springer eBooks · doi:10.1007/978-3-319-55065-7_634
Testicular Adrenal Rest Tumors and an Adrenal Nodule in a Patient with Congenital Adrenal Hyperplasia
Farnsworth, P., Schultz, E., & Rose, T. A. (2021) · Applied Radiology · doi:10.37549/ar2701
Adrenal Glands - The Current Stage and New Perspectives of Diseases and Treatment
Păun, D. L., Cianci, P., & Restini, E. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.102209 · Cited by 1
Adrenal Cortex Hormones
Al-Kaf, A. G. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.106785
Uso de plantas medicinais no tratamento da Síndrome do Ovário Policístico (SOP): Uma revisão integrativa
Albuquerque, F. N. D. N., de Araujo, K. K. B., Silva, L. V. D. S., de Siqueira, A. B. A. P., Souza, A. T. M., Magalhães, C. D. S., & Randau, K. P. (2022) · Research Society and Development · doi:10.33448/rsd-v11i13.35916 · Cited by 1
Challenges of Management of Congenital Adrenal Hyperplasia in Developing Countries
Alsaffar, H. (2022) · Journal of Diabetes and Endocrine Practice · doi:10.1055/s-0042-1758769
Iposodiemia, idroureteronefrosi e infezione delle vie urinarie: pensiamo allo pseudoipoaldosteronismo
Accomando, F., Aricò, M. O. L. R., & Marsciani, M. (2022) · QUADERNI ACP · doi:10.53141/qacp.2022.260-262
Alternative androgen pathways
Masiutin, M., & Yadav, M. (2023) · WikiJournal of Medicine · doi:10.15347/wjm/2023.003
Restos adrenales testiculares en un niño con diagnóstico de hiperplasia suprarrenal congénita clásica
Otta, C. F., Iraci, G. S., Ñañez, M., Prietto, D., & Ochoa, J. (2023) · Medicina · doi:10.23878/medicina.v24i1.1202
Study of women's knowledge of the role of androgens and their excess in women - research article
ĆWIK-BŁOTNICKA, D., & Nitka, K. (2023) · Journal of Education Health and Sport · doi:10.12775/jehs.2023.17.01.010
Az extrém fizikális és mentális terhelés, valamint az endogén szteroid bioszintézis összefüggései professzionális sportolóknál
Csöndör, É. (2023) · Pécsi Tudományegyetem · doi:10.15170/pte.2023.009
Endocrine Disorders
Sandler, C. N., & SHANK, K. R. (2024) · Springer eBooks · doi:10.1007/978-3-031-54281-7_40
A Patient with a History of Traumatic Brain Injury and Fever
An, L., Ferber, C. J., & Siddiqui, H. (2024) · Springer eBooks · doi:10.1007/978-3-031-62517-6_4
21-Hydroxylase deficiency: Clinical and biochemical aspects
Nordenström, A., & Lajić, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00171-0
Aggressive Behavior and Characteristics in Congenital Adrenal Hyperplasia
Çetin, S. K., & Aycan, Z. (2024) · Springer eBooks · doi:10.1007/978-3-031-32046-0_146-1
Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
Hawsawi, K. A. A., Qul, H., Alkhamesi, A., & Fageeh, S. M. (2025) · Cureus · doi:10.7759/cureus.79012
Gynecologic Evaluation and Diagnosis of Nonclassic Congenital Adrenal Hyperplasia
Conway, N. B., & McGovern, P. G. (2025) · Topics in Obstetrics & Gynecology · doi:10.1097/01.pgo.0001110228.39777.76
Praktisches Management des Adrenogenitalen Syndroms
Wörther, H. (2025) · Journal für Endokrinologie Diabetologie und Stoffwechsel · doi:10.1007/s41969-025-00269-3
Maternal Exposure to an Environmentally Relevant Phthalate Mixture Modulates the Steroidogenic Genes in the Adrenal Glands Throughout Postnatal Development of Male Rats
Magosso, N. S. S., de Souza, P. V., de Aquino, A. M., Rocha, V. A., Fioretto, M. N., Costa, L. G. A., Campos, S. G. P., Barbisan, L. F., Justulin, L. A., Flaws, J. A., et al. (2025) · Environmental Toxicology · doi:10.1002/tox.24545
Aggressive Behavior and Characteristics in Congenital Adrenal Hyperplasia
Çetin, S. K., & Aycan, Z. (2025) · Springer eBooks · doi:10.1007/978-3-031-73363-5_146
Hormonal Therapy and Cardiotoxicity in Prostate Cancer Patients
Muniyan, S., Xi, L., Samidurai, A., Das, A., Kukreja, R. C., & Batra, S. K. (2025) · Advances in biochemistry in health and disease · doi:10.1007/978-3-031-90598-8_16
Adrenal Disorders and Pubertal Development in Children: Hormonal Pathways, Timing Disruptions and Clinical Outcome
Soliman, A. T., Adel, A., Alyafei, F., Alaaraj, N., Hamed, N., Ahmed, S., & Elawwa, A. (2025) · GSC Advanced Research and Reviews · doi:10.30574/gscarr.2025.25.2.0361
Update in Adrenal Steroidogenesis and Congenital Adrenal Hyperplasia
Bouliari, A., Lekarev, O., & Lin‐Su, K. (2026) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2026.01.001
Rôle des voies de signalisation AMPc/PKA et Wnt/bêta-caténine dans la formation des systèmes de régulation aberrants au sein de la corticosurrénale
Mestre, J. L. (2018) · theses.fr (ABES) · doi:10.70675/cab4c4e4z049az4c9czbbefzbf46cdba1d44
The adrenal cortex exhibits sexually dimorphic tissue renewal and disease development
Grabek, A. (2019) · theses.fr (ABES) · doi:10.70675/f21bb585zdf26z43f8zbfd6z687aea86457b
Traitements maternels au long cours et développement foeto-placentaire : impact des inhibiteurs de protéases anti-VIH sur la fonction endocrine placentaire, in vitro
Fraichard, C. (2020) · theses.fr (ABES) · doi:10.70675/0c7ff667z9852z4ad9z9392z7d0b4aced00b
Classic Congenital Adrenal Hyperplasia Presenting as Primary Amenorrhea
Karthik, V., Salman, M., & Alam, A. (2026) · Bangladesh Journal of Endocrinology and Metabolism · doi:10.4103/bjem.bjem_3_26
Design and Efficacy Evaluation of CRISPR/Cas9 Guide RNAs for Knockout of the Cyp21a1 Gene in Mouse Cells and Embryos
Antonova, E. N., Uldanova, E. E., Trifonova, A. S., Piven, E. D., Глазова, О. В., Sakr, N., Rudev, N. V., Vorontsova, M. V., Митяева, О. Н., & Volchkov, P. Y. (2026) · Russian Journal of Genetics · doi:10.1134/s102279542670002x
КЛІНІЧНИЙ ВИПАДОК НЕКЛАСИЧНОЇ ФОРМИ ВРОДЖЕНОЇ ДИСФУНКЦІЇ КОРИ НАДНИРКОВИХ ЗАЛОЗ З ДЕФІЦИТОМ ФЕРМЕНТУ 21-ГІДРОКСИЛАЗИ У СПОЛУЧЕННІ З СИНДРОМОМ СПОЛУЧНОТКАНИННОЇ ДИСПЛАЗІЇ
Дорош, О., Левінтанус, В., Feskova, A., Feskov, O. M., Feskova, I., Konoplia, L., & Герасименко, Л. В. (2026) · PROBLEMS OF ENDOCRINE PATHOLOGY · doi:10.21856/j-pep.2026.2.09
Can machine learning transform the diagnostic approach to congenital disorders of adrenal steroidogenesis?
Liimatta, J. (2026) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgag269
Congenital adrenal hyperplasia in children: a comprehensive review of clinical spectrum, diagnostic strategies, and management approaches
Giri, D., Alderson, J., Bashir, M., Shalaby, M. S., Williams, C., & Park, J. (2026) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem-2026-0106
Clinical and genetic spectrum of classic congenital adrenal hyperplasia due to CYP21A2 mutations in a Taiwanese cohort
Lee, H. J., Chiu, C.-F., Huang, Y.-C., Huang, C.-C., & Lo, F. (2026) · Pediatrics & Neonatology · doi:10.1016/j.pedneo.2026.05.006
Management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update
Bobrowicz, M., Roszkowska, Z., Domański, J., Ginalska-Malinowska, M., Rak, B., Gastoł, P., Betlejewska, J., Gładka, A., Hubska, J., & Ambroziak, U. (2026) · Endokrynologia Polska · doi:10.5603/ep.110211
New perspectives on congenital adrenal hyperplasia: current concepts in pathophysiology, fertility and therapeutic advances
Szklarz, M., Wołos-Kłosowicz, K., Szulc, J., Górny, J. M., & Matuszewski, W. (2026) · Middle East Fertility Society Journal · doi:10.1186/s43043-026-00364-8
Diagnóstico y manejo de la hiperplasia suprarrenal congénita: revisión sistemática
Sanchez-Zambrano, J., Zamora-Trejo, I. B., & Castellano-Castellano, F. G. (2026) · Cuaderno de odontología. Revista científica. · doi:10.62574/sodygynv

Authors: Turcu, A. F., & Auchus, R. J.
Affiliations: University of Michigan (US)
Corresponding author: Auchus, Richard J.
ORCID: Turcu, Adina F.
Auchus, Richard J.
Venue: Endocrinology and Metabolism Clinics of North America
Publisher: Elsevier BV
Published: 2015-06
Volume: 44
Issue: 2
Pages: 275-296
ISSN: 0889-8529 (ISSN-L)
DOI: 10.1016/j.ecl.2015.02.002
PMC: PMC4506691
OpenAlex: W1958109677
Cited by: 177
References: 155
Citations by year: 2026: 14 · 2025: 15 · 2024: 20 · 2023: 19 · 2022: 23 · 2021: 12 · 2020: 17 · 2019: 19 · 2018: 18 · 2017: 8 · 2016: 10 · 2015: 1
FWCI: 1.20
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Endocrinology and Metabolism Clinics of North America (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Diabetes and Digestive and Kidney Diseases (F32DK103461)
Topics: Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal Regulation and Hypertension
Keywords: adrenal steroidogenesis, congenital adrenal hyperplasia, 21-hydroxylase deficiency, aldosterone, cortisol, dehydroepiandrosterone, adrenal androgens, mineralocorticoids, glucocorticoids, ACTH, cholesterol
MeSH terms: Adrenal Cortex Neoplasms, Adrenal Hyperplasia, Congenital, Aldosterone, Androgens, Dehydroepiandrosterone, Glucocorticoids, Humans, Hydrocortisone, Mineralocorticoids, Risk Factors, Myelolipoma, Adrenocortical Adenoma, Dehydroepiandrosterone Sulfate, Hormone Replacement Therapy

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Adrenal Steroidogenesis and Congenital Adrenal Hyperplasia

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks