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keywords > Respiratory Tract Diseases > Bronchial Diseases > Bronchiectasis > Kartagener Syndrome
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.
[Diagnostics of primary ciliary dyskinesia]
Etiology and outcome of bronchiectasis in children: a study of 41 patients.
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm.
Ultrastructural abnormalities of respiratory cilia: a 25-year experience.
These characteristic findings reveal a rare disease.
[Clinical characteristics of primary ciliary dyskinesia in children].
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia.
Structural and functional lung disease in primary ciliary dyskinesia.
Candidate gene analysis in three families with acilia syndrome.
Early adolescent primary ciliary dyskinesia associated with broncholithiasis.
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q.
Early lung disease in young children with primary ciliary dyskinesia.
Torquetenovirus infection and ciliary dysmotility in children with recurrent pneumonia.
Nasal nitric oxide for early diagnosis of familial primary ciliary dyskinesia.
Nasal nitric oxide for early diagnosis of primary ciliary dyskinesia: practical issues in children.
[Neonatal diagnosis of primary ciliary dyskinesia. Recent advances].
[Testicular seminoma in a patient with Kartagener's syndrome].