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

Year Number of Results
1985 1
1987 1
1991 1
1996 1
2003 2
2004 2
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2007 2
2008 2
2009 1
2011 3
2012 3
2014 8
2015 1
2017 5
2018 2
2019 3
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2023 2
2024 0

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43 results

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Page 1
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 sy …
However, recent studies in human patients, animal models and model organisms have indicated that there are differences in components of spec …
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. We conducted a systematic review of the literature to examine the utility of nNO in screening for PCD, in particular 1) d …
Nasal nitric oxide (nNO) concentrations are low in patients with primary ciliary dyskinesia (PCD) providing a noninvasi …
Cystic fibrosis, primary ciliary dyskinesia and non-cystic fibrosis bronchiectasis: update 2008-11.
Flight WG, Jones AM. Flight WG, et al. Thorax. 2012 Jul;67(7):645-9. doi: 10.1136/thoraxjnl-2011-200467. Epub 2011 Jun 15. Thorax. 2012. PMID: 21680564 Review.
A review is presented of key clinical papers published in Thorax and elsewhere between 2008 and April 2011 which have advanced our understanding of cystic fibrosis (CF), primary ciliary dyskinesia and non-CF bronchiectasis. Studies were identified through sea …
A review is presented of key clinical papers published in Thorax and elsewhere between 2008 and April 2011 which have advanced our understan …
Clinical care of children with primary ciliary dyskinesia.
Lucas JS, Alanin MC, Collins S, Harris A, Johansen HK, Nielsen KG, Papon JF, Robinson P, Walker WT. Lucas JS, et al. Expert Rev Respir Med. 2017 Oct;11(10):779-790. doi: 10.1080/17476348.2017.1360770. Epub 2017 Aug 2. Expert Rev Respir Med. 2017. PMID: 28745925 Review.
Primary ciliary dyskinesia (PCD) is a rare heterogeneous disorder, usually inherited as an autosomal recessive condition but X-linked inheritance is also described. Abnormal ciliary function in childhood leads to neonatal respiratory distress in term i
Primary ciliary dyskinesia (PCD) is a rare heterogeneous disorder, usually inherited as an autosomal recessive conditio
[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. ...In the PCD group, a history of neonatal respiratory distress was found in 40% of cases, 82% had had bronchopneumonia, 37% …
INTRODUCTION: Primary ciliary dyskinesia (PCD) is an inherited disease responsible for a disruption of normal ciliar
[Management of Primary Ciliary Dyskinesia].
Raidt J, Brillault J, Brinkmann F, Jung A, Koerner-Rettberg C, Koitschev A, Linz-Keul H, Nüßlein T, Ringshausen FC, Röhmel J, Rosewich M, Werner C, Omran H. Raidt J, et al. Pneumologie. 2020 Nov;74(11):750-765. doi: 10.1055/a-1235-1520. Epub 2020 Sep 25. Pneumologie. 2020. PMID: 32977348 Free PMC article. Review. German.
Primary Ciliary Dyskinesia (PCD, MIM 242650) is a rare, hereditary multiorgan disease characterized by malfunction of motile cilia. ...
Primary Ciliary Dyskinesia (PCD, MIM 242650) is a rare, hereditary multiorgan disease characterized by malfunction of m
The emerging genetics of primary ciliary dyskinesia.
Zariwala MA, Omran H, Ferkol TW. Zariwala MA, et al. Proc Am Thorac Soc. 2011 Sep;8(5):430-3. doi: 10.1513/pats.201103-023SD. Proc Am Thorac Soc. 2011. PMID: 21926394 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive, rare, genetically heterogeneous condition characterized by oto-sino-pulmonary disease together with situs abnormalities (Kartagener syndrome) owing to abnormal ciliary structure and function.
Primary ciliary dyskinesia (PCD) is an autosomal recessive, rare, genetically heterogeneous condition characterized by
[Primary ciliary dyskinesia with HYDIN gene mutations in a child and literature review].
Chen LL, Yang YG, Wu JZ, Chen XR. Chen LL, et al. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):304-307. doi: 10.3760/cma.j.issn.0578-1310.2017.04.014. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441829 Review. Chinese.
Objective: To review children's primary ciliary dyskinesia (PCD) in the pathogenesis, clinical manifestation, diagnosis and treatment. Method: To summarize and analyze the clinical data of a patient who was admitted to the first affiliated hospital of Xiamen …
Objective: To review children's primary ciliary dyskinesia (PCD) in the pathogenesis, clinical manifestation, diagnosis …
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.
Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Leigh MW, et al. Genet Med. 2009 Jul;11(7):473-87. doi: 10.1097/GIM.0b013e3181a53562. Genet Med. 2009. PMID: 19606528 Free PMC article. Review.
Primary ciliary dyskinesia is a genetically heterogeneous disorder of motile cilia. ...Clinical molecular genetic testing for primary ciliary dyskinesia is available for the most common mutations. ...
Primary ciliary dyskinesia is a genetically heterogeneous disorder of motile cilia. ...Clinical molecular genetic testi
[Cilia and renal cysts].
Paces-Fessy M. Paces-Fessy M. Med Sci (Paris). 2014 Nov;30(11):1024-33. doi: 10.1051/medsci/20143011017. Epub 2014 Nov 10. Med Sci (Paris). 2014. PMID: 25388585 Free article. Review. French.
Historically, these genes were not necessarily associated with ciliopathies, but it appeared that many connections can be made between the cystic kidney disease and function of the primary cilium. Indeed, the proteins encoded by these genes are localized to the cilium itse …
Historically, these genes were not necessarily associated with ciliopathies, but it appeared that many connections can be made between the c …
43 results