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

Pheochromocytoma associated with a succinate dehydrogenase subunit B mutation: A minireview and a case report.

Endocrine regulations - 1 Jan 2023

Rezkallah Emad, Elsaify Andrew, Martin Victorino, Viva Laura, Nag Sath, Green Barnabas, Cheesman Matthew, Elsaify Wael

Abstract excerpt

Objective. Pheochromocytomas and paragangliomas are rare neuroendocrine tumors that arise from the chromaffin cells of the adrenal medulla or extra-adrenal tissues. These tumors are characterized by an excessive secretion of catecholamines, which are responsible for the clinical manifestation of the disease. Although most of these tumors are sporadic, underlying genetic abnormalities may be present in up to 24%...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Adrenal Gland Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Catecholamines

Share to Mutation

Share to Paraganglioma

Share to Pheochromocytoma

Share to Succinate Dehydrogenase

Source

Identifiers

PMID: 37285461
DOI: 10.2478/enr-2023-0015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pheochromocytoma associated with a succinate dehydrogenase subunit B mutation: A minireview and a case report.PMID 37285461Read ↗

Pheochromocytoma: an update on genetics and management.Semantic proximity Read ↗

An Update on the Histology of Pheochromocytomas: How Does it Relate to Genetics?Semantic proximity Read ↗

A novel mutation of the succinate dehydrogenase B gene in a Korean family with pheochromocytoma.Semantic proximity Read ↗

Pheochromocytoma: The Expanding Genetic Differential DiagnosisSemantic proximity Read ↗

The occurrence of SDHB gene mutations in pheochromocytoma.Semantic proximity Read ↗

Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.Semantic proximity Read ↗

Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.Semantic proximity Read ↗

High Frequency of<i>SDHB</i>Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic TestingSemantic proximity Read ↗

Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.Semantic proximity Read ↗

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomasSemantic proximity Read ↗

Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patientsSemantic proximity Read ↗

Pheochromocytoma: A Clinicopathologic and Molecular Study of 390 Cases From a Single Center.Semantic proximity Read ↗

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