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

Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndrome

2 Aug 2020

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 and Paraganglionic Tumors
Share to Hormonal Regulation and Hypertension
Share to Pituitary Gland Disorders and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32741965
DOI: 10.1038/s41436-020-0921-3

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

Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndromePMID 32741965Read ↗

Overview of recent guidelines and consensus statements on initial screening and management of phaeochromocytoma and paraganglioma in SDHx pathogenic variant carriers and patientsSemantic proximity Read ↗

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variantsSemantic proximity Read ↗

Growth Rate of Paragangliomas Related to Germline Mutations of the SDHx GenesSemantic proximity Read ↗

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

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

UK recommendations for SDHA germline genetic testing and surveillance in clinical practice.Semantic proximity Read ↗

Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50.Semantic proximity Read ↗

Prevalence of Germline Mutations in Patients with Pheochromocytoma or Abdominal Paraganglioma and Sporadic Presentation: A Population‐Based Study in Western SwedenSemantic proximity Read ↗

Germline SDHD mutation in familial phaeochromocytomaSemantic proximity Read ↗

Trends of genetic screening in patients with pheochromocytoma and paraganglioma: 15-year experience in a high-volume tertiary referral center.Semantic proximity Read ↗

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysisSemantic proximity Read ↗

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