	Case Study: Impact of Ambassador Animal Educational Programs on Adrenal Activity. J Appl Anim Welf Sci Miller LJ, Ramont M, Morfeld KA, Chardell M. PMID: 42811673 [PubMed - as supplied by publisher]
	Trajectory-based analysis of growth in congenital adrenal hyperplasia: therapeutic implications for final height preservation. Eur J Pediatr Gawlik Z, Gawlik J, Tyrawa K, Starzyk J, Janu. PMID: 42811175 [PubMed - indexed for MEDLINE]
	Efficacy and Safety of Adrenal Artery Embolization for Idiopathic Hyperaldosteronism: A Systematic Review & Meta-Analysis. Cardiovasc Intervent Radiol Teixeira EG, Duran R, Barra F, Hezel IM, Germano VPO, Rivera M, Giancristoforo BCA. PMID: 42811134 [PubMed - as supplied by publisher]
	Differential Diagnosis of ACTH-Dependent Hypercortisolism: Case Report and Literature Review. Rev Med Chil Oksenberg S, Nilo F, Villanueva P, Hernández MI, González C, Cruz JP, Baudrand R, Uslar T, Domínguez JM, Guarda FJ. PMID: 42809788 [PubMed - indexed for MEDLINE]
	Diagnostic Accuracy Study of Morning Salivary Cortisone for Screening Adrenal Insufficiency in a Real-World Cohort. J Clin Endocrinol Metab Televantos C, Monaghan PJ, Michaelidou M, Chen LR, Ahmed M, Ho JH, Dhage S, Higham C, Keevil B, Adam S. PMID: 42806822 [PubMed - as supplied by publisher]
	Mild autonomous cortisol secretion (MACS) is associated with increased mortality in patients with adrenal adenomas only in the presence of type 2 diabetes: a retrospective cohort study. Cardiovasc Diabetol Bellach L, Hofer-Zeni S, Sluková D, Kalender D, Zimmermann C, Michler N, Gard L, Baumgartner-Parzer S, Marculescu R, Vila G, Wolf P, Kautzky-Willer A, Leutner M. PMID: 42806332 [PubMed - indexed for MEDLINE]
	Primary adrenal lymphoma presenting as primary adrenal insufficiency. BMJ Case Rep Ahmed K, Stratos E, Saada L, Cunningham J, Myint KS. PMID: 42805623 [PubMed - indexed for MEDLINE]
	The cardiometabolic significance of post-dexamethasone cortisol levels below the MACS threshold in adrenal incidentaloma. Endocrine Korkmaz ES, Öztürk Gökçe B, Kebapç. PMID: 42804108 [PubMed - indexed for MEDLINE]
	Multi-biomarker models based on the androgen backdoor pathway for diagnosing 17Î±-hydroxylase/17,20-lyase deficiency. Endocrine Liu Y, Cai S, Zhang T, Sun S, Kong X, Zhou J, Chen B, Li Z. PMID: 42804103 [PubMed - indexed for MEDLINE]
	Adrenal Rest Tumors and the clinical course of gonadal dysfunction in adult men with Congenital Adrenal Hyperplasia caused by 21-Hydroxylase Deficiency: A single-center experience with long-term follow-up. Endocrine Ozturk Unsal I, Koray Fedai N, Hepsen S, Ucan B, Ozbek M, Cakal E. PMID: 42804041 [PubMed - indexed for MEDLINE]
	Newborn screening for congenital adrenal hyperplasia: a 3 years study embedded in 25 years of regional experience in Italy. Endocrine Tuli G, Munarin J, Pavanello E, De Sanctis L. PMID: 42803878 [PubMed - indexed for MEDLINE]
	Self-Perception of Reproductive Health, Mental Health, and Quality of Life in Females With Classical Congenital Adrenal Hyperplasia: A Systematic Review. J ASEAN Fed Endocr Soc Tenaya WJ, Nugraha M, Susanto JV, Liu AF, Wijaya SR, Pramono LA. PMID: 42802773 [PubMed - indexed for MEDLINE]
	Prevalence, risk factors, and the screening value of basal cortisol for adrenal insufficiency after corticosteroid therapy in children with idiopathic nephrotic syndrome. Clin Exp Nephrol Konatala TS, Dawman L, Vallabhaneni P, Tiewsoh K, Yadav J, Sachdeva N. PMID: 42801413 [PubMed - as supplied by publisher]
	Letter to the Editor from ErdoÄŸan Ã–zbuÄŸday and Karakurt: "Primary adrenal insufficiency resulting in diagnosis of rare ABCD1 pathogenic variant in X-linked adrenoleukodystrophy". JCEM Case Rep Erdo, Karakurt F. PMID: 42798852 [PubMed]
	High metanephrines with adrenal hemorrhage: a diagnostic dilemma. JCEM Case Rep Ortega Abad M, Eldib M, Fretes Oviedo N, Rao PPR. PMID: 42798807 [PubMed]
	Transition from Pediatric to Adult Endocrine Care in Patients with Congenital Adrenal Hyperplasia: A Single-Center Retrospective Analysis. Medicina (Kaunas) Mercan Sar, Karatoprak K, Nursoy H, Hocao, Ya, Denkboy Öngen Y, Cander S, Ertürk E, Öz Gül Ö, Eren E, Ersoy C. PMID: 42796361 [PubMed - indexed for MEDLINE]
	Novel Compound Heterozygous NNT Variants in Familial Glucocorticoid Deficiency Type 4 Diagnosed by Whole Genome Sequencing. Ann Clin Lab Sci Cho WK, Jang S, Youn E, Cheon CK. PMID: 42790937 [PubMed - indexed for MEDLINE]
	Assessment, External Verification and Modification of Models in Diagnosing Primary Aldosteronism Subtypes. J Clin Hypertens (Greenwich) Jing Y, Zhang Y, Guo H, Hou R, Xu J, Wang J, Pan X, Niu X, Song L, Huang L, Zhang J, Jia F, Sun B, Wang N. PMID: 42789381 [PubMed - indexed for MEDLINE]
	A structured approach to address variability in the global management of adrenal insufficiency in Duchenne muscular dystrophy: the 2025 PJ Nicholoff steroid protocol. Front Neurol Sbrocchi AM, Ahmet A, Kinnett K, Lautatzis ME, McMillan HJ, Apkon S, Rutter MM, Ward LM, Bowden SA, Connolly AM, Noritz G, Schrader R, Selby K, Veerapandiyan A, Wong SC, Weber DR. PMID: 42787106 [PubMed - indexed for MEDLINE]
	ERBB4 and Neurodegeneration: Association Between Hypothalamic-Pituitary-Adrenal (HPA) Axis: Associated Neurodegenerative Pathogenesis. Cells Bagyinszky E, An SSA. PMID: 42782811 [PubMed - indexed for MEDLINE]

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