The genetic basis of pheochromocytoma: who to screen and how?

doi:10.1038/ncpendmet0097

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

Community

Back to search

Article

The genetic basis of pheochromocytoma: who to screen and how?

Nature clinical practice. Endocrinology & metabolism - 1 Feb 2006

Plouin Pierre-François, Gimenez-Roqueplo Anne-Paule

Abstract excerpt

No abstract is available from the source.

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 Mutation
Share to Pheochromocytoma
Share to Proto-Oncogene Proteins c-ret

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Succinate Dehydrogenase

Source

Open in PubMed

Identifiers

PMID: 16932255
DOI: 10.1038/ncpendmet0097

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The genetic basis of pheochromocytoma: who to screen and how?PMID 16932255Read ↗

Pheochromocytoma: A Genetic And Diagnostic UpdateSemantic proximity Read ↗

Genetic Testing for PheochromocytomaSemantic proximity Read ↗

Inherited Mutations in Pheochromocytoma and Paraganglioma: Why All Patients Should Be Offered Genetic TestingSemantic proximity Read ↗

[Genetic diagnosis of pheochromocytoma].Semantic proximity Read ↗

Genetics of pheochromocytomas and paragangliomasSemantic proximity Read ↗

Genetic and epigenetic profile of sporadic pheochromocytomas.Semantic proximity Read ↗

Pheochromocytoma: When to search a germline defect?Semantic proximity Read ↗

An update on the genetics of pheochromocytoma.Semantic proximity Read ↗

65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma.Semantic proximity Read ↗

Clinical and molecular markers guide the genetics of pheochromocytoma and paraganglioma.Semantic proximity Read ↗

What is the role of genetic testing in diagnosis of haemochromatosis?Semantic proximity Read ↗

Genetic basis of phaeochromocytoma and paragangliomaSemantic proximity Read ↗

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