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1976 1
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1998 1
2000 2
2004 2
2005 3
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2012 2
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56 results

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Page 1
Motile ciliopathies.
Wallmeier J, Nielsen KG, Kuehni CE, Lucas JS, Leigh MW, Zariwala MA, Omran H. Wallmeier J, et al. Nat Rev Dis Primers. 2020 Sep 17;6(1):77. doi: 10.1038/s41572-020-0209-6. Nat Rev Dis Primers. 2020. PMID: 32943623 Review.
If mucociliary clearance in the respiratory epithelium is severely impaired, the disorder is referred to as primary ciliary dyskinesia, the most common motile ciliopathy. No single test can confirm a diagnosis of motile ciliopathy, which is based on a combina …
If mucociliary clearance in the respiratory epithelium is severely impaired, the disorder is referred to as primary ciliary
[Respiratory physiotherapy in pediatric practice].
Audag N, Dubus JC, Combret Y. Audag N, et al. Rev Mal Respir. 2022 Jun;39(6):547-560. doi: 10.1016/j.rmr.2022.05.001. Epub 2022 Jun 21. Rev Mal Respir. 2022. PMID: 35738979 Review. French.
For LRT clearance, several indications, such as cystic fibrosis, primary ciliary dyskinesia and neuromuscular disease, are now widely advocated. ...
For LRT clearance, several indications, such as cystic fibrosis, primary ciliary dyskinesia and neuromuscular disease, …
Dandy-Walker Malformation.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B38-B41. doi: 10.1016/j.ajog.2020.08.184. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168220 Review. No abstract available.
Nasal nitric oxide screening for primary ciliary dyskinesia: systematic review and meta-analysis.
Collins SA, Gove K, Walker W, Lucas JS. Collins SA, et al. Eur Respir J. 2014 Dec;44(6):1589-99. doi: 10.1183/09031936.00088614. Epub 2014 Oct 16. Eur Respir J. 2014. PMID: 25323224 Free article. Review.
Nasal nitric oxide (nNO) concentrations are low in patients with primary ciliary dyskinesia (PCD) providing a noninvasive screening test. ...Meta-analysis of 11 studies comparing nNO during a velum closure breath hold gave a meanSD nNO of 19.418.6 nL.m …
Nasal nitric oxide (nNO) concentrations are low in patients with primary ciliary dyskinesia (PCD) providing a noninvasi …
[Primary ciliary dyskinesia: a retrospective review of clinical and paraclinical data].
Beucher J, Chambellan A, Segalen J, Deneuville E. Beucher J, et al. Rev Mal Respir. 2011 Sep;28(7):856-63. doi: 10.1016/j.rmr.2011.02.014. Epub 2011 Sep 3. Rev Mal Respir. 2011. PMID: 21943530 Review. French.
INTRODUCTION: Primary ciliary dyskinesia (PCD) is an inherited disease responsible for a disruption of normal ciliary function. ...These subjects had defects in ciliary structure, 59% in the dynein arms, 35% in the central complex and 6% …
INTRODUCTION: Primary ciliary dyskinesia (PCD) is an inherited disease responsible for a disruption of normal ciliar
Induced Pluripotent Stem Cells for Primary Ciliary Dyskinesia Modeling and Personalized Medicine.
Mianné J, Ahmed E, Bourguignon C, Fieldes M, Vachier I, Bourdin A, Assou S, De Vos J. Mianné J, et al. Am J Respir Cell Mol Biol. 2018 Dec;59(6):672-683. doi: 10.1165/rcmb.2018-0213TR. Am J Respir Cell Mol Biol. 2018. PMID: 30230352 Free article. Review.
Primary ciliary dyskinesia (PCD) is a rare and heterogeneous genetic disorder that affects the structure and function of motile cilia. In the airway epithelium, impaired ciliary motion results in reduced or absent mucociliary clearance that leads to th
Primary ciliary dyskinesia (PCD) is a rare and heterogeneous genetic disorder that affects the structure and function o
Primary ciliary dyskinesia complicated with diffuse panbronchiolitis: a case report and literature review.
Chen W, Shao C, Song Y, Bai C. Chen W, et al. Clin Respir J. 2014 Oct;8(4):425-30. doi: 10.1111/crj.12089. Epub 2014 Jan 10. Clin Respir J. 2014. PMID: 24308375 Free PMC article. Review.
BACKGROUND: Fifty percent of patients with primary ciliary dyskinesia (PCD) have situs inversus. Diffuse panbronchiolitis (DPB) might be one of the characteristic features of the lung in PCD. METHODS: We reported a case of PCD without situs inversus, yet comp …
BACKGROUND: Fifty percent of patients with primary ciliary dyskinesia (PCD) have situs inversus. Diffuse panbronchiolit …
Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia. A Systematic Review and Meta-analysis.
Shapiro AJ, Josephson M, Rosenfeld M, Yilmaz O, Davis SD, Polineni D, Guadagno E, Leigh MW, Lavergne V. Shapiro AJ, et al. Ann Am Thorac Soc. 2017 Jul;14(7):1184-1196. doi: 10.1513/AnnalsATS.201701-062SR. Ann Am Thorac Soc. 2017. PMID: 28481653 Free PMC article. Review.
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disorder causing chronic otosinopulmonary disease, generally diagnosed through evaluation of respiratory ciliary ultrastructure and/or genetic testing. ...In 12 study populations (1,344 patients com …
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disorder causing chronic otosinopulmonary disease, generally diag …
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease.
Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW. Knowles MR, et al. Am J Respir Crit Care Med. 2013 Oct 15;188(8):913-22. doi: 10.1164/rccm.201301-0059CI. Am J Respir Crit Care Med. 2013. PMID: 23796196 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia that leads to oto-sino-pulmonary diseases and organ laterality defects in approximately 50% of cases. ...Recent studies, using advanced imaging and pulmonary ph
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia that leads to oto-si
Nasal versus tracheobronchial biopsies to diagnose primary ciliary dyskinesia: A meta-analysis.
Adil EA, Kawai K, Dombrowski N, Irace AL, Cunningham MJ. Adil EA, et al. Laryngoscope. 2017 Jan;127(1):6-13. doi: 10.1002/lary.26070. Epub 2016 Jun 16. Laryngoscope. 2017. PMID: 27312809 Review.
OBJECTIVES/HYPOTHESIS: To systematically review the literature regarding the efficacy of different biopsy sites and methods to obtain an adequate ciliary sample for ultrastructural examination with electron microscopy (EM) for the diagnosis of primary ciliary
OBJECTIVES/HYPOTHESIS: To systematically review the literature regarding the efficacy of different biopsy sites and methods to obtain an ade …
56 results