Literature DB >> 6225657

Pathophysiology of the ciliary motility syndromes.

H Levison, C M Mindorff, J Chao, J A Turner, J M Sturgess, D A Stringer.   

Abstract

The ciliary motility syndromes are characterised by specific and genetically determined defects of cilia with resulting impairment of mucociliary defense mechanisms in the respiratory tract. The ciliary pathobiology, clinical observations, serial pulmonary function and chest radiographs are reviewed and correlated for a series of 33 patients with the ciliary motility syndromes, aged from 0.5 to 75 years. The clinical course and progressive nature of this disease emphasizes the importance of early and accurate diagnosis to prevent irreversible pulmonary damage.

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Year:  1983        PMID: 6225657

Source DB:  PubMed          Journal:  Eur J Respir Dis Suppl        ISSN: 0106-4347


  5 in total

1.  Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung.

Authors:  J F Poschet; J C Boucher; L Tatterson; J Skidmore; R W Van Dyke; V Deretic
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

2.  Exhaled nitric oxide in paediatric asthma and cystic fibrosis.

Authors:  J O Lundberg; S L Nordvall; E Weitzberg; H Kollberg; K Alving
Journal:  Arch Dis Child       Date:  1996-10       Impact factor: 3.791

Review 3.  Primary ciliary dyskinesia.

Authors:  L Le Mauviel
Journal:  West J Med       Date:  1991-09

4.  Ultrastructure and mucociliary transport of bronchial respiratory epithelium in intubated patients.

Authors:  F Konrad; R Schiener; T Marx; M Georgieff
Journal:  Intensive Care Med       Date:  1995-06       Impact factor: 17.440

5.  Enhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2.

Authors:  Casey W McKenzie; Joshua M Klonoski; Taylor Maier; Glenda Trujillo; Peter F Vitiello; Victor C Huber; Lance Lee
Journal:  Cilia       Date:  2013-12-20
  5 in total

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