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

Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman.

Endocrine pathology - 1 Jan 2003

Weinhäusel Andreas, Behmel Annemarie, Ponder Bruce A J, Haas Oskar A, Niederle Bruno, Gessl Alois, Vierhapper Heinrich, Pfragner Roswitha

Abstract excerpt

A unilateral, apparently sporadic pheochromocytoma was removed from the right adrenal of a 73-yr-old Caucasian woman. At the time of surgery, germline DNA from the patient was not available. However, a continuous cell line (KNA) established from the tumor showed a heterozygous sequence variant TG...

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 Calcitonin
Share to Carcinoma, Medullary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple Endocrine Neoplasia Type 2a

Share to Pheochromocytoma

Share to Proto-Oncogene Mas

Share to Proto-Oncogene Proteins c-ret

Share to Thyroidectomy

Source

Identifiers

PMID: 14739494
DOI: 10.1385/ep:14:4:375

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14739494-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman.PMID 14739494Read ↗

Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large family.Semantic proximity Read ↗

A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A.Semantic proximity Read ↗

Mutations in the RET protooncogene in sporadic pheochromocytomas.Semantic proximity Read ↗

Mutations in the cysteine-rich region of the RET proto-oncogene in patients diagnosed as having sporadic medullary thyroid carcinoma.Semantic proximity Read ↗

Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type.Semantic proximity Read ↗

Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe.Semantic proximity Read ↗

[Phenotype of the C634Y mutation in the RET proto-oncogene in MEN2A: report of a family].Semantic proximity Read ↗

A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC.Semantic proximity Read ↗

Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.Semantic proximity Read ↗

A family of multiple endocrine neoplasia type 2A (MEN 2A) with Cys630Tyr RET germline mutation: report of a case.Semantic proximity Read ↗

A novel mutation (D631del) of the RET gene was associated with MEN2A in a Chinese pedigree.Semantic proximity Read ↗

A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene.Semantic proximity Read ↗

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