Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

doi:10.1093/qjmed/89.9.653

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Article

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

QJM : monthly journal of the Association of Physicians - 1 Sept 1996

Trump D, Farren B, Wooding C, Pang J T, Besser G M, Buchanan K D, Edwards C R, Heath D A, Jackson C E, Jansen S, Lips K, Monson J P, O'Halloran D, Sampson J, Shalet S M, Wheeler M H, Zink A, Thakker R V

Abstract excerpt

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of parathyroid, pancreatic islet and anterior pituitary tumours. To facilitate a screening programme for MEN1, we investigated 709 people (364 males and 345 females, age range 1-8...

Topics

Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Child
Child, Preschool
Female
Humans
Hypercalcemia
Hyperparathyroidism
Infant
Male
Middle Aged
Models, Genetic

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Multiple Endocrine Neoplasia Type 1

Mutation

Pancreatic Neoplasms

Source

Open in PubMed

Identifiers

PMID: 8917740
DOI: 10.1093/qjmed/89.9.653

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8917740-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.