• <em>MAX</em> germline mutation-associated pheochromocytoma-paraganglioma syndrome: multiple endocrine neoplasia type 5
• A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas
• A rare association of pheochromocytoma, paraganglioma, and pituitary adenoma (3PA): A case report and literature review
• Acromegaly
• An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline <em>SDHB</em> pathogenic variant in the absence of paraganglioma or pheochromocytoma
• Aortic dissection due to primary aldosteronism in a young adult with adrenal adenoma: A case report
• Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review
• Carney Complex
• Case report: Two sisters with a germline <em>CHEK2</em> variant and distinct endocrine neoplasias
• Characteristics of Bilateral Adrenal Lesions: Experience from an Indian Tertiary Care Centre
• Clinical and genetic analysis of a case of Gitelman syndrome accompanied with Graves disease and adrenocortical adenoma: A case report
• Clinical and genetic analysis of a case of Gitelman syndrome with comorbid Graves disease and adrenocortical adenoma
• Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents
• Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival
• Conn Syndrome
• Diagnosis, Management, and Follow-Up of the Incidentally Discovered Adrenal Mass: CUA Guideline Endorsed by the AUA
• Expression of Amine Oxidase Proteins in Adrenal Cortical Neoplasm and Pheochromocytoma
• Expressions of Cushing's syndrome in multiple endocrine neoplasia type 1
• Extensive expertise in endocrinology: glucose-dependent insulinotropic peptide-dependent Cushing's syndrome
• Familial Hyperaldosteronism Type 3 with a Rapidly Growing Adrenal Tumor: An In Situ Aldosterone Imaging Study
• Familial Isolated Pituitary Adenoma
• Gardner Syndrome
• Genetic predisposition to pheochromocytoma and paraganglioma: 21 years of experience in the field
• MEN1 in a Patient With Nonsyndromic Familial Nonmedullary Thyroid Carcinoma
• Metabolic syndrome and Visceral Adiposity Index in non-functional adrenal adenomas
• Multiple endocrine neoplasia type 1 with Zollinger-Ellison syndrome: clinicopathological analysis of a Japanese family with focus on menin immunohistochemistry
• Pathogenesis of Primary Aldosteronism: Impact on Clinical Outcome
• Pathology and gene mutations of aldosterone-producing lesions
• Rare correlation of somatic PRKACA mutations with pregnancy-associated aldosterone- and cortisol-producing adenomas: a case report and literature review
• Rare forms of hereditary endocrine neoplasia: co-existence of pituitary adenoma and pheochromocytoma/paraganglioma
• Surgical removal of a giant non-functional adrenal mass: A case report
• The mystery of transient pregnancy-induced cushing's syndrome: a case report and literature review highlighting GNAS somatic mutations and LHCGR overexpression
• The protean role of Val804Met RET mutation in thyroid neoplasms: An example of a "MEN2C" syndrome?
• Unveiling the Significance of NCAP Family Genes in Adrenocortical Carcinoma and Adenoma Pathogenesis: A Molecular Bioinformatics Exploration
• Update on the Genetics of Primary Aldosteronism and Aldosterone-Producing Adenomas
• What We Know about and What Is New in Primary Aldosteronism
• Who should be screened for primary aldosteronism? A comprehensive review of current evidence
• Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma