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Last Updated: 10/31/2025
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Found 1813 publications
CCDC39 Mutation-Related Primary Ciliary Dyskinesia with Congenitally Corrected Transposition of the Great Arteries: A Case Report.
Journal: The American journal of case reports
Published: October 13, 2025
EFCAB10 anchors AK8 to the radial spoke for proper ciliary motility.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 07, 2025
Primary ciliary dyskinesia with situs inversus totalis.
Journal: BMJ case reports
Published: September 29, 2025
Primary ciliary dyskinesia phenotypes and correlation with genotype.
Journal: Current opinion in pulmonary medicine
Published: September 15, 2025
Kartagener syndrome with main complaint of nasal obstruction: a case report
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: September 01, 2025
Adequacy of Clinical and Radiological Evidence for the Management of Kartagener Syndrome.
Journal: Cureus
Published: August 27, 2025
Situs inversus totalis with pleural empyema: a clue to ciliary dysfunction.
Journal: BMJ case reports
Published: August 21, 2025
A Case of Kartagener's Syndrome Presenting With Severe Hypoxemia.
Journal: Cureus
Published: August 12, 2025
Kartagener's syndrome with congenital heart defect-an old rare disease with a new rare face.
Journal: Cardiology in the young
Published: August 11, 2025
Clinical and genetic analysis of a case of Kartagener syndrome with obstructive azoospermia induced by biallelic variation of CCDC114
Journal: Zhonghua nan ke xue = National journal of andrology
Published: August 10, 2025
Kartagener Syndrome in Two Siblings: A Familial Case Report With Phenotypic Variability and Destroyed Lung Syndrome as a Rare Complication.
Journal: Cureus
Published: July 20, 2025
Last Updated: 10/31/2025