Disease: Adrenal adenoma- familial
- A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas
- 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
- Carney Complex
- Case report: Two sisters with a germline <em>CHEK2</em> variant and distinct endocrine neoplasias
- 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
- 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
- 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 forms of hereditary endocrine neoplasia: co-existence of pituitary adenoma and pheochromocytoma/paraganglioma
- 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?
- 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