Associated Papers
Genetics and clinical characteristics of Korean patients with bilateral macronodular adrenocortical disease.
Park SS et al.
European Journal of Endocrinology, 2026
A Global Approach to the Long-Term Follow-up of 17 Families with Bilateral Macronodular Adrenal Disease.
Charchar HLS et al.
The Journal of Clinical Endocrinology and Metabolism, 2025
Advancements in the research of the structure, function, and disease-related roles of ARMC5.
Qu Y et al.
Frontiers of Medicine, 2025
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.
Bouys L et al.
Orphanet Journal of Rare Diseases, 2025
ARMC5 mutations are associated with high levels of proliferating cell nuclear antigen and the presence of the serotonin receptor 5HT4R in PMAH nodules.
Conceição BBD et al.
Archives of Endocrinology and Metabolism, 2020
Molecular mechanisms of ARMC5 mutations in adrenal pathophysiology.
Stratakis CA et al.
Current Opinion in Endocrine and Metabolic Research, 2019
Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma.
Elbelt U et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation.
Faucz FR et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
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