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

PRECISION MEDICINE: AN UPDATE ON GENOTYPE/BIOCHEMICAL PHENOTYPE RELATIONSHIPS IN PHEOCHROMOCYTOMA/PARAGANGLIOMA PATIENTS.

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists - 1 Jun 2017

Gupta Garima, Pacak Karel

Abstract excerpt

OBJECTIVE: Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors known to produce and secrete high levels of circulating catecholamines and their metabolites. The biochemical characteristics of these tumors can be used to divide them into three major phenotypes. The adrenergic, noradrenergic and dopaminergic phenotypes are defined by predominant elevations in epinephrine and metanephrine,...

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 Dopamine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Epinephrine

Share to Genotype

Share to Norepinephrine

Share to Paraganglioma

Share to Pheochromocytoma

Share to Precision Medicine

Source

Open in PubMed Open full text

Identifiers

PMID: 28332883
DOI: 10.4158/EP161718.RA
PMCID: PMC7470624

Genes

EPAS1
PNMT
RET
SDHAF2
VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PRECISION MEDICINE: AN UPDATE ON GENOTYPE/BIOCHEMICAL PHENOTYPE RELATIONSHIPS IN PHEOCHROMOCYTOMA/PARAGANGLIOMA PATIENTS.PMID 28332883Read ↗

Pheochromocytoma–Paraganglioma Syndrome: A Multiform Disease with Different Genotype and Phenotype FeaturesSemantic proximity Read ↗

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

Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours.Semantic proximity Read ↗

Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.Semantic proximity Read ↗

Pheochromocytoma: implications in tumorigenesis and the actual management.Semantic proximity Read ↗

Hypoxia Pathway Mutations in Pheochromocytomas and Paragangliomas.Semantic proximity Read ↗

New Perspectives on Pheochromocytoma and Paraganglioma: Toward a Molecular Classification.Semantic proximity Read ↗

Pheochromocytomas and Paragangliomas: An Update on Recent Molecular Genetic Advances and Criteria for Malignancy.Semantic proximity Read ↗

Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.Semantic proximity Read ↗

Risk Stratification on Pheochromocytoma and Paraganglioma from Laboratory and Clinical MedicineSemantic proximity Read ↗

Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new eraSemantic proximity Read ↗

Molecular markers of paragangliomas/pheochromocytomas.Semantic proximity Read ↗

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