[Various neuroendocrine tumors in a family with multiple endocrine neoplasia type 1].

doi:10.1556/OH.2013.29772

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

Back to search

Article

[Various neuroendocrine tumors in a family with multiple endocrine neoplasia type 1].

Orvosi hetilap - 22 Dec 2013

Sepp Krisztián, Valkusz Zsuzsanna

Abstract excerpt

When multiple endocrine tumors are detected more tests are required to diagnose endocrine tumor syndromes. The authors report the case history of a patient with clinical manifestation of multiplex endocrine neoplasia type 1 (parathyroid adenoma, pancreatic neuroendocrine tumor, pituitary tumor, adrenal gland tumors and thymic neuroendocrine carcinoma). Genetic screening proved a novel stop codon mutation of the...

Topics

Adenoma
Adrenal Gland Neoplasms
Adult
Humans
Magnetic Resonance Imaging
Male
Multiple Endocrine Neoplasia Type 1
Mutation
Neuroendocrine Tumors
Pancreatic Neoplasms
Parathyroid Neoplasms
Pituitary Neoplasms
Positron-Emission Tomography
Thymus Neoplasms
Tomography, X-Ray Computed

Source

Open in PubMed

Identifiers

PMID: 24334135
DOI: 10.1556/OH.2013.29772

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics