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

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

Annales d'endocrinologie - 1 Jan 1998

Richard S, Giraud S, Beroud C, Caron J, Penfornis F, Baudin E, Niccoli-Sire P, Murat A, Schlumberger M, Plouin P F, Conte-Devolx B

Abstract excerpt

Von Hippel-Lindau (VHL) disease is an autosomal dominant disorder, predisposing to the development of central nervous system (CNS) and retinal hemangioblastomas, endolymphatic sac tumors, renal cell carcinoma and/or renal cysts, pheochromocytomas, pancreatic cysts and/or tumors. Incidence of the disease is 1/36,000. CNS hemangioblastomas and renal cell carcinoma are the main causes of death. The VHL gene, located...

Read the complete abstract on PubMed

Topics

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

Share to Carcinoma, Renal Cell
Share to Cerebellar Neoplasms

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to VHL gene

Share to Hemangioblastoma

Share to Kidney Neoplasms

Share to Mutation

Share to von Hippel-Lindau Disease

Source

Identifiers

PMID: 10189987

Genes

VHL

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Von Hippel-Lindau disease: recent genetic progress and patient management. Francophone Study Group of von Hippel-Lindau Disease (GEFVH)].PMID 10189987Read ↗

[Von Hippel-Lindau disease and central nervous system hemangioblastoma. Progress in genetics and clinical management].Semantic proximity Read ↗

[Von Hippel-Lindau disease and renal cancer: 10 years of genetic progress. GEFVHL (French-Speaking Study Group on von Hippel-Lindau disease)].Semantic proximity Read ↗

[von Hippel-Lindau disease].Semantic proximity Read ↗

[Von Hippel-Lindau syndrome - two sides of the same coin].Semantic proximity Read ↗

von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance.Semantic proximity Read ↗

Genetics, Pathophysiology, and Current Challenges in Von Hippel-Lindau Disease TherapeuticsSemantic proximity Read ↗

von Hippel-Lindau disease: a clinical and scientific review.Semantic proximity Read ↗

[A Family case of von Hippel-Lindau syndrome].Semantic proximity Read ↗

Von Hippel–Lindau Disease: Molecular Pathological Basis, Clinical Criteria, Genetic Testing, Clinical Features of Tumors and TreatmentSemantic proximity Read ↗

Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia Syndrome.Semantic proximity Read ↗

Management of von Hippel-Lindau Disease: An Interdisciplinary ReviewSemantic proximity Read ↗

Von Hippel-Lindau syndrome. A pleomorphic condition.Semantic proximity Read ↗

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