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

Clinical Manifestations and Genotype of Primary Ciliary Dyskinesia Diagnosed in Korea: Multicenter Study

1 Jan 2023

Abstract excerpt

PURPOSE: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder that leads to secondary ciliary dysfunction. PCD is a rare disease, and data on it are limited in Korea. This study systematically evaluated the clinical symptoms, diagnostic characteristics, and treatment modalities of pediatric PCD in Korea. METHODS: This Korean nationwide, multicenter study, conducted between January 2000 and...

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis Research Advances
Share to Respiratory viral infections research
Share to Tracheal and airway disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37957793
DOI: 10.4168/aair.2023.15.6.757

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Manifestations and Genotype of Primary Ciliary Dyskinesia Diagnosed in Korea: Multicenter StudyPMID 37957793Read ↗

Clinical manifestations and genotype of primary ciliary dyskinesia diagnosed in Korea: a nationwide, multicenter, retrospective studySemantic proximity Read ↗

Clinical phenotypes of primary ciliary dyskinesia.Semantic proximity Read ↗

Primary Ciliary Dyskinesia: A Rare and Often Underdiagnosed Disease.Semantic proximity Read ↗

Clinical and genetic spectrum of primary ciliary dyskinesia in Chinese patients: a systematic review.Semantic proximity Read ↗

Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.Semantic proximity Read ↗

Clinical features and genetic spectrum of children with primary ciliary dyskinesia in central China: a referral center retrospective analysisSemantic proximity Read ↗

Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey.Semantic proximity Read ↗

Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment StrategiesSemantic proximity Read ↗

Primary ciliary dyskinesia.Semantic proximity Read ↗

Primary Ciliary Dyskinesia.Semantic proximity Read ↗

Exploring Rare Genetic Mutations in PCD: A Study of 8 Turkish Patients with Novel Gene Alterations Coupled by Their Ciliary Beat Frequency and Confocal Microscopy AnalysesSemantic proximity Read ↗

ERS and ATS diagnostic guidelines for primary ciliary dyskinesia: similarities and differences in approach to diagnosisSemantic proximity Read ↗

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