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

18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma.

The Journal of clinical endocrinology and metabolism - 1 Apr 2018

Taïeb David, Jha Abhishek, Guerin Carole, Pang Ying, Adams Karen T, Chen Clara C, Romanet Pauline, Roche Philippe, Essamet Wassim, Ling Alexander, Quezado Martha M, Castinetti Frédéric, Sebag Fréderic, Pacak Karel

Abstract excerpt

Context: MYC-associated factor X (MAX) has been recently described as a new susceptibility pheochromocytoma (PHEO) gene with a total of ~40 reported cases. At present, no study has specifically described the functional imaging phenotype of MAX-related PHEO. Objective, Patients, and Design: The objective of the present study was to present our experience with contrast-enhanced computed tomography (CT) and...

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 Basic Helix-Loop-Helix Leucine Zipper Transcription Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dihydroxyphenylalanine

Share to MAX gene

Share to Mutation

Share to Pheochromocytoma

Share to Positron Emission Tomography Computed Tomography

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 29534198
DOI: 10.1210/jc.2017-02324
PMCID: PMC6276705

Genes

MAX
MYC

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma.PMID 29534198Read ↗

MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Clinical description & molecular modeling of novel MAX pathogenic variant causing pheochromocytoma in family, supports paternal parent-of-origin effect.Semantic proximity Read ↗

Recent Advances in Genetics, Diagnosis, Localization, and Treatment of PheochromocytomaSemantic proximity Read ↗

Genotype and clinical phenotype characteristics of MAX germline mutation-associated pheochromocytoma/paraganglioma syndrome.Semantic proximity Read ↗

Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation.Semantic proximity Read ↗

Quantitative 18F-DOPA PET/CT in pheochromocytoma: the relationship between tumor secretion and its biochemical phenotype.Semantic proximity Read ↗

Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5?Semantic proximity Read ↗

A Novel MAX Gene Mutation Variant in a Patient With Multiple and "Composite" Neuroendocrine-Neuroblastic Tumors.Semantic proximity Read ↗

Pheochromocytomas in Multiple Endocrine Neoplasia Type 2.Semantic proximity Read ↗

Expanding the phenotype of multiple endocrine neoplasia type 5 (MEN5): Pituitary gigantism, myelolipoma and familial pheochromocytoma due to a germline pathogenic MAX variant.Semantic proximity Read ↗

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.Semantic proximity Read ↗

A Novel Phenotype of Germline Pathogenic Variants in MAX: Concurrence of Pheochromocytoma and Ganglioneuroma in a Chinese Family and Literature Review.Semantic proximity Read ↗

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