Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1992 1
1998 1
1999 1
2000 1
2003 1
2006 1
2007 1
2010 2
2013 1
2014 2
2015 1
2016 4
2017 1
2018 1
2022 1
2023 3
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

22 results

Results by year

Filters applied: . Clear all
Page 1
Clinical and genetic spectrum of primary ciliary dyskinesia in Chinese patients: a systematic review.
Peng B, Gao YH, Xie JQ, He XW, Wang CC, Xu JF, Zhang GJ. Peng B, et al. Orphanet J Rare Dis. 2022 Jul 19;17(1):283. doi: 10.1186/s13023-022-02427-1. Orphanet J Rare Dis. 2022. PMID: 35854386 Free PMC article. Review.
BACKGROUND: Primary ciliary dyskinesia (PCD) represents a highly heterogenous disorder with extensive clinical and genetic patterns among populations of different geographic location and ethnic origin. ...RESULTS: A total of 244 Chinese PCD patients in 52 art …
BACKGROUND: Primary ciliary dyskinesia (PCD) represents a highly heterogenous disorder with extensive clinical and gene …
Primary Ciliary Dyskinesia: A Clinical Review.
Despotes KA, Zariwala MA, Davis SD, Ferkol TW. Despotes KA, et al. Cells. 2024 Jun 4;13(11):974. doi: 10.3390/cells13110974. Cells. 2024. PMID: 38891105 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, motile ciliopathy, characterized by neonatal respiratory distress, recurrent upper and lower respiratory tract infections, subfertility, and laterality defects. ...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, motile ciliopathy, characterized by neonatal res
Ear and upper airway clinical outcome measures for use in primary ciliary dyskinesia research: a scoping review.
Alexandru M, Veil R, Rubbo B, Goutaki M, Kim S, Lam YT, Nevoux J, Lucas JS, Papon JF. Alexandru M, et al. Eur Respir Rev. 2023 Jul 12;32(169):220200. doi: 10.1183/16000617.0200-2022. Print 2023 Sep 30. Eur Respir Rev. 2023. PMID: 37437912 Free PMC article. Review.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by pulmonary, otological and sino-nasal manifestations. ...RESULTS: 33 studies (1794 patients) were included. 10 ear and upper airway outcomes were reported. 17 studies repo …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by pulmonary, otological and sino …
Gasotransmitter Research Advances in Respiratory Diseases.
Jiang S, Chen H, Shen P, Zhou Y, Li Q, Zhang J, Chen Y. Jiang S, et al. Antioxid Redox Signal. 2024 Jan;40(1-3):168-185. doi: 10.1089/ars.2023.0410. Epub 2023 Dec 8. Antioxid Redox Signal. 2024. PMID: 37917094 Review.
Gasotransmitters play a role in various respiratory diseases such as asthma, chronic obstructive pulmonary disease, obstructive sleep apnea, lung infection, bronchiectasis, cystic fibrosis, primary ciliary dyskinesia, and COVID-19. Recent Advances: Gasotransm …
Gasotransmitters play a role in various respiratory diseases such as asthma, chronic obstructive pulmonary disease, obstructive sleep apnea, …
Primary ciliary dyskinesia: recent advances in pathogenesis, diagnosis and treatment.
Lie H, Ferkol T. Lie H, et al. Drugs. 2007;67(13):1883-92. doi: 10.2165/00003495-200767130-00006. Drugs. 2007. PMID: 17722956 Review.
Primary ciliary dyskinesia is a genetic disorder causing dysfunctional motility of cilia and impaired mucociliary clearance, resulting in a myriad of clinical manifestations including recurrent sinopulmonary disease, laterality defects and infertility.
Primary ciliary dyskinesia is a genetic disorder causing dysfunctional motility of cilia and impaired mucociliar
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 …
Delivery of Alpha-1 Antitrypsin to Airways.
Griese M, Scheuch G. Griese M, et al. Ann Am Thorac Soc. 2016 Aug;13 Suppl 4:S346-51. doi: 10.1513/AnnalsATS.201507-469KV. Ann Am Thorac Soc. 2016. PMID: 27564672 Review.
Treatment with exogenous alpha-1 antitrypsin (AAT), a potent serine protease inhibitor, was developed originally for chronic obstructive pulmonary disease associated with AAT deficiency; however, other lung conditions involving neutrophilic inflammation and proteolytic tissue inj …
Treatment with exogenous alpha-1 antitrypsin (AAT), a potent serine protease inhibitor, was developed originally for chronic obstructive pul …
Toward an Earlier Diagnosis of Primary Ciliary Dyskinesia. Which Patients Should Undergo Detailed Diagnostic Testing?
Kuehni CE, Lucas JS. Kuehni CE, et al. Ann Am Thorac Soc. 2016 Aug;13(8):1239-43. doi: 10.1513/AnnalsATS.201605-331PS. Ann Am Thorac Soc. 2016. PMID: 27258773 Free article. Review.
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cilia, leading to chronic upper and lower respiratory symptoms. ...The sensitivity and specificity of the tools are reasonable, but positive and negative predicti
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cilia, leading to chro
Picking up speed: advances in the genetics of primary ciliary dyskinesia.
Horani A, Brody SL, Ferkol TW. Horani A, et al. Pediatr Res. 2014 Jan;75(1-2):158-64. doi: 10.1038/pr.2013.200. Epub 2013 Nov 5. Pediatr Res. 2014. PMID: 24192704 Free PMC article. Review.
Abnormal ciliary axonemal structure and function are linked to the growing class of genetic disorders collectively known as ciliopathies, and our understanding of the complex genetics and functional phenotypes of these conditions has rapidly expanded. While progress …
Abnormal ciliary axonemal structure and function are linked to the growing class of genetic disorders collectively known as ci …
Rare lung diseases I--Lymphangioleiomyomatosis.
Juvet SC, Hwang D, Downey GP. Juvet SC, et al. Can Respir J. 2006 Oct;13(7):375-80. doi: 10.1155/2006/696573. Can Respir J. 2006. PMID: 17036091 Free PMC article. Review.
The first article is on lymphangioleiomyomatosis (LAM); subsequent articles will focus on pulmonary alveolar proteinosis, alpha-1-antitrypsin deficiency and primary ciliary dyskinesia. LAM is a rare, progressive and (without intervention) often fatal intersti …
The first article is on lymphangioleiomyomatosis (LAM); subsequent articles will focus on pulmonary alveolar proteinosis, alpha-1-antitrypsi …
22 results