Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1976
2025

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

Year Number of Results
1976 1
1979 2
1980 2
1981 2
1982 2
1983 6
1984 8
1985 6
1986 4
1987 3
1988 16
1989 6
1990 7
1991 7
1992 3
1993 2
1994 5
1995 6
1996 5
1997 3
1998 8
1999 9
2000 20
2001 11
2002 3
2003 7
2004 16
2005 11
2006 21
2007 24
2008 13
2009 25
2010 18
2011 26
2012 25
2013 17
2014 28
2015 28
2016 29
2017 31
2018 22
2019 21
2020 22
2021 25
2022 24
2023 24
2024 25
2025 2

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

566 results

Results by year

Filters applied: . Clear all
Page 1
Understanding Primary Ciliary Dyskinesia and Other Ciliopathies.
Horani A, Ferkol TW. Horani A, et al. J Pediatr. 2021 Mar;230:15-22.e1. doi: 10.1016/j.jpeds.2020.11.040. Epub 2020 Nov 23. J Pediatr. 2021. PMID: 33242470 Free PMC article. Review.
Ciliopathies are a collection of disorders related to cilia dysfunction. Cilia are specialized organelles that project from the surface of most cells. ...Our understanding of the genetics, pathophysiology, and clinical manifestations of motile ciliopathies, including prima …
Ciliopathies are a collection of disorders related to cilia dysfunction. Cilia are specialized organelles that project from the surfa …
Ciliopathies and the Kidney: A Review.
McConnachie DJ, Stow JL, Mallett AJ. McConnachie DJ, et al. Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9. Am J Kidney Dis. 2021. PMID: 33039432 Free article. Review.
During the past 2 decades, they have been found to play important roles in tissue development and signal transduction, with mutations in ciliary-associated proteins resulting in a group of diseases collectively known as ciliopathies. Many of these mutations manifest as ren …
During the past 2 decades, they have been found to play important roles in tissue development and signal transduction, with mutations in …
Bronchiectasis.
Magis-Escurra C, Reijers MH. Magis-Escurra C, et al. BMJ Clin Evid. 2015 Feb 25;2015:1507. BMJ Clin Evid. 2015. PMID: 25715965 Free PMC article. Review.
It may complicate respiratory conditions such as asthma or COPD. It can be associated with primary ciliary dyskinesia, primary immunodeficiencies, certain systemic diseases such as inflammatory bowel disease and rheumatoid arthritis, and foreign body inhalation. ...
It may complicate respiratory conditions such as asthma or COPD. It can be associated with primary ciliary dyskinesia, primary …
Primary ciliary dyskinesia.
Raidt J, Loges NT, Olbrich H, Wallmeier J, Pennekamp P, Omran H. Raidt J, et al. Presse Med. 2023 Sep;52(3):104171. doi: 10.1016/j.lpm.2023.104171. Epub 2023 Jul 27. Presse Med. 2023. PMID: 37516247 Review.
BACKGROUND AND OBJECTIVES: Primary ciliary dyskinesia (PCD, ORPHA:244) is a group of rare genetic disorders characterized by dysfunction of motile cilia. ...It is critical that we continue to expand our knowledge of this group of rare disorders to impr …
BACKGROUND AND OBJECTIVES: Primary ciliary dyskinesia (PCD, ORPHA:244) is a group of rare genetic disorders characteriz …
Current and Future Treatments in Primary Ciliary Dyskinesia.
Paff T, Omran H, Nielsen KG, Haarman EG. Paff T, et al. Int J Mol Sci. 2021 Sep 11;22(18):9834. doi: 10.3390/ijms22189834. Int J Mol Sci. 2021. PMID: 34575997 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic ciliopathy in which mucociliary clearance is disturbed by the abnormal motion of cilia or there is a severe reduction in the generation of multiple motile cilia. ...
Primary ciliary dyskinesia (PCD) is a rare genetic ciliopathy in which mucociliary clearance is disturbed by the abnormal moti …
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 respirator …
Diagnosis of Primary Ciliary Dyskinesia.
Goutaki M, Shoemark A. Goutaki M, et al. Clin Chest Med. 2022 Mar;43(1):127-140. doi: 10.1016/j.ccm.2021.11.008. Clin Chest Med. 2022. PMID: 35236553 Free article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patients. ...
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patients. ...
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.
Genetic mutations (usually with autosomal recessive inheritance) that impair ciliary beating cause a variety of motile ciliopathies, a heterogeneous group of rare disorders. ...With the exception of azithromycin, there is no evidence-based treatment for primary c
Genetic mutations (usually with autosomal recessive inheritance) that impair ciliary beating cause a variety of motile ciliopathies, …
Cystic fibrosis and primary ciliary dyskinesia: Similarities and differences.
Pereira R, Barbosa T, Cardoso AL, Sá R, Sousa M. Pereira R, et al. Respir Med. 2023 Apr;209:107169. doi: 10.1016/j.rmed.2023.107169. Epub 2023 Feb 22. Respir Med. 2023. PMID: 36828173 Free article. Review.
Cystic fibrosis (CF) and Primary ciliary dyskinesia (PCD) are both rare chronic diseases, inherited disorders associated with multiple complications, namely respiratory complications, due to impaired mucociliary clearance that affect severely patients' lives. …
Cystic fibrosis (CF) and Primary ciliary dyskinesia (PCD) are both rare chronic diseases, inherited disorders associate …
Primary ciliary dyskinesia in the genomics age.
Lucas JS, Davis SD, Omran H, Shoemark A. Lucas JS, et al. Lancet Respir Med. 2020 Feb;8(2):202-216. doi: 10.1016/S2213-2600(19)30374-1. Epub 2019 Oct 14. Lancet Respir Med. 2020. PMID: 31624012 Review.
Primary ciliary dyskinesia is a genetically and clinically heterogeneous syndrome. Impaired function of motile cilia causes failure of mucociliary clearance. ...Developments in genomics and molecular medicine are rapidly improving diagnosis, and a genetic cause can …
Primary ciliary dyskinesia is a genetically and clinically heterogeneous syndrome. Impaired function of motile cilia causes fa …
566 results