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

Year Number of Results
1980 1
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2015 3
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Page 1
[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 …
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 …
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 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 …
Diagnostic approach to primary ciliary dyskinesia: a review.
Holzmann D, Ott PM, Felix H. Holzmann D, et al. Eur J Pediatr. 2000 Jan-Feb;159(1-2):95-8. doi: 10.1007/pl00013813. Eur J Pediatr. 2000. PMID: 10653339 Review.
Primary ciliary dyskinesia (PCD) is a heterogeneous disease with impaired mucociliary transport leading to respiratory disorders, hearing impairment and male infertility. ...All were thoroughly examined for other possible diseases before biopsy, and te …
Primary ciliary dyskinesia (PCD) is a heterogeneous disease with impaired mucociliary transport leading to respiratory …
Impact of primary ciliary dyskinesia: Beyond sinobronchial syndrome in Japan.
Keicho N, Hijikata M, Miyabayashi A, Wakabayashi K, Yamada H, Ito M, Morimoto K. Keicho N, et al. Respir Investig. 2024 Jan;62(1):179-186. doi: 10.1016/j.resinv.2023.12.005. Epub 2023 Dec 28. Respir Investig. 2024. PMID: 38154292 Review.
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterized by impaired motile cilia function, particularly in the upper and lower airways. ...In Japan, homozygosity for a 27.7-kb deletion of DRC1 is estimated to be the most common cause …
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterized by impaired motile cilia function, particular …
Full-Term Neonatal Respiratory Distress and Chronic Lung Disease.
Chowdhury N, Giles BL, Dell SD. Chowdhury N, et al. Pediatr Ann. 2019 Apr 1;48(4):e175-e181. doi: 10.3928/19382359-20190328-01. Pediatr Ann. 2019. PMID: 30986319 Review.
Respiratory distress occurs in 5% to 7% of live births at term gestation. Most cases are mild and transient and can be attributed to transient tachypnea of the newborn or "wet lung." ...Occasionally, term neonatal respiratory distress is associated with an inherited pri …
Respiratory distress occurs in 5% to 7% of live births at term gestation. Most cases are mild and transient and can be attributed to …
Underlying causes and outcomes of recurrent pneumonia in hospitalized children.
Mei M, Dai D, Guo Z, Zhang C, Liu J, Qi Y, Wang X, Wang L, Qian L. Mei M, et al. Pediatr Pulmonol. 2023 Jun;58(6):1674-1682. doi: 10.1002/ppul.26374. Epub 2023 Mar 21. Pediatr Pulmonol. 2023. PMID: 36919525 Review.
The associations between factors and adverse outcomes were assessed using logistic regression. RESULTS: Of 551 children with RP, 483 (87.7%) manifested underlying causes, with recurrent aspiration (127, 23.0%), primary immunodeficiency (PID) (91, 16.5%), and congeni …
The associations between factors and adverse outcomes were assessed using logistic regression. RESULTS: Of 551 children with RP, 483 (87. …
Recognizing genetic disease: A key aspect of pediatric pulmonary care.
Yonker LM, Hawley MH, Moschovis PP, Lu M, Kinane TB. Yonker LM, et al. Pediatr Pulmonol. 2020 Jul;55(7):1794-1809. doi: 10.1002/ppul.24706. Pediatr Pulmonol. 2020. PMID: 32533909 Free PMC article. Review.
Increased familiarity with these conditions allows for improved care of these patients by reducing time to diagnosis, tailoring management, and prompting further investigation into these disorders....
Increased familiarity with these conditions allows for improved care of these patients by reducing time to diagnosis, tailoring management, …
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 …
31 results