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Article

Identification of Clinical Relevant Molecular Subtypes of Pheochromocytoma.

Frontiers in endocrinology - 1 Jan 2021

Saddozai Umair Ali Khan, Wang Fengling, Akbar Muhammad Usman, Zhang Lu, An Yang, Zhu Wan, Xie Longxiang, Li Yongqiang, Ji Xinying, Guo Xiangqian

Abstract excerpt

Pheochromocytoma (PCC) is a rare neuroendocrine tumor of the adrenal gland with a high rate of mortality if diagnosed at a late stage. Common symptoms of pheochromocytoma include headache, anxiety, palpitation, and diaphoresis. Different treatments are under observation for PCC but there is still no effective treatment option. Recently, the gene expression profiling of various tumors has provided new...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 34234737
DOI: 10.3389/fendo.2021.605797
PMCID: PMC8256389

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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