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

Renovascular hypertension and RNF213 p.R4810K variant in Korean children with Moyamoya disease.

Clinical nephrology - 1 Aug 2021

Kim Jeong Yeon, Cho Heeyeon

Abstract excerpt

Moyamoya disease (MMD) is the most common underlying disease in Korean pediatric renovascular hypertension (RVH). The ring finger protein 213 (RNF213) p.R4810K variant is reported to be a pathologic variant in East Asian MMD. The purpose of this study was to evaluate hypertension (HTN) prevalence and clinical manifestations as well as RNF213 p.R4810K variant prevalence in Korean pediatric MMD patients. The...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine Triphosphatases
Share to Child
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Moyamoya Disease

Share to Republic of Korea

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 33769276
DOI: 10.5414/CN110334

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Renovascular hypertension and RNF213 p.R4810K variant in Korean children with Moyamoya disease.PMID 33769276Read ↗

Validation and Extension Study Exploring the Role of RNF213 p.R4810K in 2,877 Chinese Moyamoya Disease Patients.Semantic proximity Read ↗

Role of Ring Finger Protein 213 in Moyamoya Disease.Semantic proximity Read ↗

Moyamoya Disease and Spectrums of RNF213 Vasculopathy.Semantic proximity Read ↗

RNF213-Related Vasculopathy: Various Systemic Vascular Diseases Involving RNF213 Gene Mutations: Review.Semantic proximity Read ↗

Difference in Clinical Phenotype, Mutation Position, and Structural Change of RNF213 Rare Variants Between Pediatric and Adult Japanese Patients with Moyamoya Disease.Semantic proximity Read ↗

The Susceptibility Pathogenesis of Moyamoya Disease.Semantic proximity Read ↗

The Association of Heterozygous p.R4810K of RNF213 and Long-Term Unfavorable Outcomes after Encephaloduroarteriosynangiosis in Chinese Pediatric Patients with Moyamoya Disease.Semantic proximity Read ↗

RNF213 and cardiovascular disease: A review of histopathological, genetic perspectives, and potential molecular mechanisms.Semantic proximity Read ↗

Frequency of the moyamoya-related RNF213 p.Arg4810Lys variant in 1,516 Korean individualsSemantic proximity Read ↗

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.Semantic proximity Read ↗

An Overview of Genetics of Moyamoya: Beyond RNF213 Gene.Semantic proximity Read ↗

Adult Moyamoya Disease and Moyamoya Syndrome: What Is New?Semantic proximity Read ↗

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