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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 21
2019 20
2020 21
2021 24
2022 22
2023 22
2024 5

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540 results

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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 …
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. ...
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 …
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 …
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 …
[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, are now …
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. ...Next-generation sequencing has increased gene discovery, and mutations in more than 40 genes have been reported to cause primary ciliary dyskinesia, with many other g …
Primary ciliary dyskinesia is a genetically and clinically heterogeneous syndrome. ...Next-generation sequencing has increased …
Sperm defects in primary ciliary dyskinesia and related causes of male infertility.
Sironen A, Shoemark A, Patel M, Loebinger MR, Mitchison HM. Sironen A, et al. Cell Mol Life Sci. 2020 Jun;77(11):2029-2048. doi: 10.1007/s00018-019-03389-7. Epub 2019 Nov 28. Cell Mol Life Sci. 2020. PMID: 31781811 Free PMC article. Review.
However, recent studies in human patients, animal models and model organisms have indicated that there are differences in components of specific structures within the cilia and sperm tail axonemes. Primary ciliary dyskinesia (PCD) is a genetic disease with symptoms …
However, recent studies in human patients, animal models and model organisms have indicated that there are differences in components of spec …
540 results