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

1988
2025

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

Year Number of Results
1988 1
1989 1
1990 1
1994 1
1999 1
2000 1
2004 1
2005 1
2010 1
2014 2
2016 1
2017 3
2019 1
2020 1
2021 1
2022 2
2023 2
2024 2
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

22 results

Results by year

Filters applied: . Clear all
Page 1
Primary ciliary dyskinesia in Japan: systematic review and meta-analysis.
Inaba A, Furuhata M, Morimoto K, Rahman M, Takahashi O, Hijikata M, Knowles MR, Keicho N. Inaba A, et al. BMC Pulm Med. 2019 Jul 25;19(1):135. doi: 10.1186/s12890-019-0897-4. BMC Pulm Med. 2019. PMID: 31345208 Free PMC article.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder. Although the genetic tests and new diagnostic algorithms have recently been recommended, clinical signs and electron microscope (EM) findings have historically been the mainstays of diag …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder. Although the genetic tests and new diagnostic …
In children with primary ciliary dyskinesia, which type of lung function test is the earliest determinant of decline in lung health: A systematic review.
Zafar A, Hall M. Zafar A, et al. Pediatr Pulmonol. 2023 Feb;58(2):475-483. doi: 10.1002/ppul.26213. Epub 2022 Nov 2. Pediatr Pulmonol. 2023. PMID: 36268989
BACKGROUND: Primary ciliary dyskinesia is a rare genetic disorder characterized by recurrent sinopulmonary infections and worsening obstructive lung disease. ...RESULTS: After screening for the duplication of results and applying inclusion and exclusion crite …
BACKGROUND: Primary ciliary dyskinesia is a rare genetic disorder characterized by recurrent sinopulmonary infections a …
The patient's experience of primary ciliary dyskinesia: a systematic review.
Behan L, Rubbo B, Lucas JS, Dunn Galvin A. Behan L, et al. Qual Life Res. 2017 Sep;26(9):2265-2285. doi: 10.1007/s11136-017-1564-y. Epub 2017 Mar 30. Qual Life Res. 2017. PMID: 28361274 Free PMC article. Review.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary disease, with symptoms starting soon after birth. The aim of this study is to critically review, analyse, and synthesise the literature in order …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary dise …
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. ...OBJECTIVES: To perform a systematic review …
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disorder causing chronic otosinopulmonary disease, generally diag …
Gene mutations in primary ciliary dyskinesia related to otitis media.
Mata M, Milian L, Armengot M, Carda C. Mata M, et al. Curr Allergy Asthma Rep. 2014 Mar;14(3):420. doi: 10.1007/s11882-014-0420-1. Curr Allergy Asthma Rep. 2014. PMID: 24459089 Review.
Otitis media with effusion (OME) is the most common cause of conductive hearing loss in children and is strongly associated with primary ciliary dyskinesia (PCD). Approximately half of the children with PCD require otolaryngology care, posing a major problem …
Otitis media with effusion (OME) is the most common cause of conductive hearing loss in children and is strongly associated with primary
Bacterial infections in patients with primary ciliary dyskinesia: Comparison with cystic fibrosis.
Wijers CD, Chmiel JF, Gaston BM. Wijers CD, et al. Chron Respir Dis. 2017 Nov;14(4):392-406. doi: 10.1177/1479972317694621. Epub 2017 Mar 6. Chron Respir Dis. 2017. PMID: 29081265 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder associated with severely impaired mucociliary clearance caused by defects in ciliary structure and function. ...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder associated with severely impaired mucociliary clear
Intermittent prophylactic antibiotics for bronchiectasis.
Spencer S, Donovan T, Chalmers JD, Mathioudakis AG, McDonnell MJ, Tsang A, Leadbetter P. Spencer S, et al. Cochrane Database Syst Rev. 2022 Jan 5;1(1):CD013254. doi: 10.1002/14651858.CD013254.pub2. Cochrane Database Syst Rev. 2022. PMID: 34985761 Free PMC article. Review.
We excluded studies where participants received high dose antibiotics immediately prior to enrolment or those with a diagnosis of cystic fibrosis, allergic bronchopulmonary aspergillosis (ABPA), primary ciliary dyskinesia, hypogammaglobulinaemia, sarcoidosis, …
We excluded studies where participants received high dose antibiotics immediately prior to enrolment or those with a diagnosis of cystic fib …
Electronic Nose and Exhaled Breath NMR-based Metabolomics Applications in Airways Disease.
Santini G, Mores N, Penas A, Capuano R, Mondino C, Trové A, Macagno F, Zini G, Cattani P, Martinelli E, Motta A, Macis G, Ciabattoni G, Montuschi P. Santini G, et al. Curr Top Med Chem. 2016;16(14):1610-30. doi: 10.2174/1568026616666151223113540. Curr Top Med Chem. 2016. PMID: 26693732 Review.
E-noses and NMR-based metabolomics of EBC can distinguish patients with respiratory diseases such as asthma, COPD, and lung cancer, or diseases with a clinically relevant respiratory component including cystic fibrosis and primary ciliary dyskinesia, and heal …
E-noses and NMR-based metabolomics of EBC can distinguish patients with respiratory diseases such as asthma, COPD, and lung cancer, or disea …
Primary ciliary dyskinesia and Young's syndrome.
Smallman LA. Smallman LA. Clin Otolaryngol Allied Sci. 1989 Jun;14(3):271-8. doi: 10.1111/j.1365-2273.1989.tb00372.x. Clin Otolaryngol Allied Sci. 1989. PMID: 2663254 Review. No abstract available.
Anesthetic Management of Patients With Kartagener Syndrome: A Systematic Review of 99 Cases.
Cheng L, Dong Y, Liu S. Cheng L, et al. J Cardiothorac Vasc Anesth. 2023 Jun;37(6):1021-1025. doi: 10.1053/j.jvca.2023.01.033. Epub 2023 Feb 3. J Cardiothorac Vasc Anesth. 2023. PMID: 36849313 Review.
The most common surgical procedures were thoracic surgery (51.5%), which was followed by ear, nose, and throat surgery (16.5%), and general surgery (14.5%). The preoperative treatment of the patients was reported in only 20 patients, and included antibiotics, bronchodilato …
The most common surgical procedures were thoracic surgery (51.5%), which was followed by ear, nose, and throat surgery (16.5%), and general …
22 results