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Article

Multiple endocrine neoplasia syndrome: genetic basis for clinical management.

Current opinion in oncology - 1 Jan 2005

Carling Tobias

Abstract excerpt

PURPOSE OF REVIEW: Multiple endocrine neoplasia (MEN) types 1 and 2 are rare hereditary cancer syndromes expressing a variety of mainly endocrine neoplasias. Improved understanding of the molecular and clinical genetics associated with these lesions will likely enhance the diagnosis and treatment of patients with these diseases. RECENT FINDINGS: The MEN1 gene causing MEN1 is a tumor suppressor gene and seems to...

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Source

Identifiers

PMID: 15608505
DOI: 10.1097/01.cco.0000148567.29850.31

Genes

MEN1
RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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