Genetics, diagnosis and future treatment strategies for primary ciliary dyskinesia
Author:
Publisher
Informa Healthcare
Subject
Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
http://www.tandfonline.com/doi/pdf/10.1517/21678707.2015.989212
Reference95 articles.
1. Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children
2. Primary ciliary dyskinesia: current state of the art
3. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
4. Genetic Defects in Ciliary Structure and Function
5. Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis;Frontiers in Genetics;2022-02-28
2. Anxiety and depression in Dutch patients with primary ciliary dyskinesia and their caregivers: associations with health-related quality of life;ERJ Open Research;2021-07-22
3. The Antimicrobial Activity of Peripheral Blood Neutrophils Is Altered in Patients with Primary Ciliary Dyskinesia;International Journal of Molecular Sciences;2021-06-08
4. Genetic Anomalies of the Respiratory Tract;Current Respiratory Medicine Reviews;2020-01-01
5. Primary ciliary dyskinesia (PCD): A genetic disorder of motile cilia;Translational Science of Rare Diseases;2019-07-04
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