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

Pheochromocytoma in von Hippel-Lindau disease: clinical presentation and mutation analysis in a large, multigenerational kindred.

The Journal of clinical endocrinology and metabolism - 1 Jan 1998

Atuk N O, Stolle C, Owen J A, Carpenter J T, Vance M L

Abstract excerpt

The clinical presentation and characterization of the mutation in members of a large kindred with von Hippel-Lindau disease (VHLD) and pheochromocytoma were examined. Twenty-five proven cases of VHLD occurring in four generations of a large kindred have been followed since 1964, and pheochromocytoma has occurred in 17. Symptoms of pheochromocytoma developed at an early age, on average at 12.5 +/- 1.3 yr, and...

Read the complete abstract on PubMed

Topics

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

Share to Adenoma
Share to Adolescent
Share to Age of Onset

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Infant

Share to Kidney Neoplasms

Source

Identifiers

PMID: 9435426
DOI: 10.1210/jcem.83.1.4479

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Pheochromocytoma in von Hippel-Lindau disease: clinical presentation and mutation analysis in a large, multigenerational kindred.PMID 9435426Read ↗

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.Semantic proximity Read ↗

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.Semantic proximity Read ↗

New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense MutationsSemantic proximity Read ↗

Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings.Semantic proximity Read ↗

Clinical review 155: Pheochromocytoma in Von Hippel-Lindau disease.Semantic proximity Read ↗

Germ-Line Mutations in Nonsyndromic PheochromocytomaSemantic proximity Read ↗

[Von Hippel-Lindau disease: recent genetic progress and patient management. Francophone Study Group of von Hippel-Lindau Disease (GEFVH)].Semantic proximity Read ↗

Genetic analysis of von Hippel-Lindau disease.Semantic proximity Read ↗

Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype.Semantic proximity Read ↗

Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.Semantic proximity Read ↗

Phaeochromocytoma in children.Semantic proximity Read ↗

Pediatric pheochromocytoma in association with Von Hippel-Lindau disease: Focus on screening strategies.Semantic proximity Read ↗

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