Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multiple endocrine neoplasia 2A (MEN 2A) syndrome.

Bratislavske lekarske listy - 1 Jan 2018

Breza J, Breza J

Abstract excerpt

INTRODUCTION: In the MEN 2A syndrome, which is the most common of the three types of MEN, three endocrine systems are affected simultaneously or subsequently by the development of tumours manifested by medullary thyroid gland carcinoma, pheochromocytoma (often bilateral) and hyperparathyroidism. MATERIAL AND METHODS: 27 patients from 3 families affected by MEN 2A syndrome were examined clinically (by detecting...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adrenal Gland Neoplasms
Share to Adrenalectomy
Share to Carcinoma, Neuroendocrine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple Endocrine Neoplasia Type 2a

Share to Pheochromocytoma

Share to Positron Emission Tomography Computed Tomography

Share to Proto-Oncogene Proteins c-ret

Share to Radiopharmaceuticals

Source

Identifiers

PMID: 29455549
DOI: 10.4149/BLL_2018_034

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple endocrine neoplasia 2A (MEN 2A) syndrome.PMID 29455549Read ↗

Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study.Semantic proximity Read ↗

Genetic and Clinical Features of Multiple Endocrine Neoplasia Types 1 and 2Semantic proximity Read ↗

Catecholamine crisis as a first manifestation of familial bilateral pheochromocytoma caused by RET proto-oncogene mutation in codon C 634R.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2A. Study of a family.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2.Semantic proximity Read ↗

[Multiple endocrine neoplasia type 2].Semantic proximity Read ↗

[Multiple endocrine neoplasia type 2].Semantic proximity Read ↗

Update on multiple endocrine neoplasia Type 1 and 2.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2: 2007 update.Semantic proximity Read ↗

[Multiple endocrine neoplasia type 2].Semantic proximity Read ↗

Multiple endocrine neoplasia type 2A: case report.Semantic proximity Read ↗

[The clinical patterns and RET proto-oncogene identification of pheochromocytoma in 13 multiple endocrine neoplasia type 2A pedigrees].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.