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

Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.

Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih - 1 Dec 2009

Tong An-li, Zeng Zheng-pei, Zhou Ya-ru, Yuan Tao, Cao Cai-xia, Zhang Jing, Li Ming

Abstract excerpt

OBJECTIVE: To investigate the clinical and genetic features of a Chinese family with von Hippel-Lindau (VHL) disease revealed by bilateral pheochromocytoma. METHODS: The proband and other members in a Chinese family with familial pheochromocytoma were clinically evaluated and followed up. Genomic...

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 VHL gene
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pheochromocytoma

Share to Tomography, X-Ray Computed

Share to von Hippel-Lindau Disease

Share to Von Hippel-Lindau Tumor Suppressor Protein

Source

Identifiers

PMID: 20120764
DOI: 10.1016/s1001-9294(10)60001-6

Genes

VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20120764-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.PMID 20120764Read ↗

Clinical and genetic investigation of a multi-generational Chinese family afflicted with Von Hippel-Lindau disease.Semantic proximity Read ↗

Familial and genetic researches on three Chinese families with von Hippel-Lindau disease.Semantic proximity Read ↗

Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease.Semantic proximity Read ↗

The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.Semantic proximity Read ↗

Genotype-phenotype correlations in Chinese von Hippel-Lindau disease patients.Semantic proximity Read ↗

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

[Familial and genetic study in a large Chinese kindred with von Hippel-Lindau disease and gene mutation analysis].Semantic proximity Read ↗

Genetic study of a large Chinese kindred with von Hippel-Lindau disease.Semantic proximity Read ↗

Clinical and mutation analysis of four Chinese families with von Hippel-Lindau disease.Semantic proximity Read ↗

Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients.Semantic proximity Read ↗

VHL gene mutation analysis of a Chinese family with non- syndromic pheochromocytomas and patients with apparently sporadic pheochromocytoma.Semantic proximity Read ↗

Molecular genetic analysis and mutation screening of the VHL gene in a Japanese family with von Hippel-Lindau disease.Semantic proximity Read ↗

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