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

Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.

Familial cancer - 1 Jun 2014

Jasperson Kory W, Kohlmann Wendy, Gammon Amanda, Slack Heidi, Buchmann Luke, Hunt Jason, Kirchhoff Anne C, Baskin Henry, Shaaban Akram, Schiffman Joshua D

Abstract excerpt

Patients with germline mutations in one of the SDH genes are at substantially increased risk of developing paragangliomas, pheochromocytomas (pheos), and other tumors (all combined referred to as SDH-related tumors). However, limited data exist on screening in SDH mutation carriers and no studies...

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 Catecholamines
Share to Chromogranin A

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Early Detection of Cancer

Share to Pheochromocytoma

Share to Sensitivity and Specificity

Share to Succinate Dehydrogenase

Share to Vas Deferens

Source

Identifiers

PMID: 23934599
DOI: 10.1007/s10689-013-9639-6

Genes

SDHB
SDHC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23934599-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.PMID 23934599Read ↗

Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase mutations.Semantic proximity Read ↗

International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriersSemantic proximity Read ↗

Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.Semantic proximity Read ↗

Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.Semantic proximity Read ↗

[Hereditary pheochromocytoma and paraganglioma: screening and follow-up strategies in asymptomatic mutation carriers].Semantic proximity Read ↗

Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.Semantic proximity Read ↗

Imaging of Pheochromocytoma and ParagangliomaSemantic proximity Read ↗

Whole-Body MRI Surveillance of Cancer Predisposition Syndromes: Current Best Practice Guidelines for Use, Performance, and Interpretation.Semantic proximity Read ↗

Imaging of cancer predisposition syndromes.Semantic proximity Read ↗

Molecular imaging in hereditary succinate dehydrogenase mutation-related paragangliomas.Semantic proximity Read ↗

High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.Semantic proximity Read ↗

Paraganglioma: the role of genetic counselling and radiological screening.Semantic proximity Read ↗

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