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

Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2

31 Mar 2009

Abstract excerpt

BACKGROUND: Head and neck paragangliomas (HNPs) occur as sporadic or familial entities, the latter mostly in association with germline mutations of the SDHB, SDHC, or SDHD (SDHx) genes. Heritable non-SDHx HNP might occur in von Hippel-Lindau disease (VHL, VHL gene), multiple endocrine neoplasia type 2 (MEN2, RET gene), and neurofibromatosis type 1 (NF1, NF1 gene). Reports of non-SDHx HNP presentations are scarce...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal and Paraganglionic Tumors
Share to Cancer, Hypoxia, and Metabolism
Share to Pituitary Gland Disorders and Treatments

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19336503
DOI: 10.1210/jc.2009-0354

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2PMID 19336503Read ↗

Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.Semantic proximity Read ↗

The Changing Paradigm of Head and Neck Paragangliomas: What Every Otolaryngologist Needs to Know.Semantic proximity Read ↗

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.Semantic proximity Read ↗

Genetics of hereditary head and neck paragangliomasSemantic proximity Read ↗

Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma.Semantic proximity Read ↗

Head and neck paragangliomas in Norway, importance of genetics, updated diagnostic workup and treatment.Semantic proximity Read ↗

Head and neck paragangliomas: Report of 175 patients (1989-2010).Semantic proximity Read ↗

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.Semantic proximity Read ↗

Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients.Semantic proximity Read ↗

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.Semantic proximity Read ↗

Necessity for long-term follow-up of patients with head and neck paraganglioma and mutation in the succinate dehydrogenase genes: an index case report and literature review.Semantic proximity Read ↗

Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple DecadesSemantic proximity Read ↗

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