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Quoted phrase not found in phrase index: "Ciliary dyskinesia, primary, 39"
Page 1
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.
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 congenital heart diseases (63, 11.4%) being the most common. ...PID odds ratio (OR, 7.9; 95% confidence inter …
RESULTS: Of 551 children with RP, 483 (87.7%) manifested underlying causes, with recurrent aspiration (127, 23.0%), primary immunodef …
Primary ciliary dyskinesia and neonatal respiratory distress.
Mullowney T, Manson D, Kim R, Stephens D, Shah V, Dell S. Mullowney T, et al. Pediatrics. 2014 Dec;134(6):1160-6. doi: 10.1542/peds.2014-0808. Pediatrics. 2014. PMID: 25422025 Free PMC article.
BACKGROUND AND OBJECTIVE: Primary ciliary dyskinesia (PCD) is a rare inherited disease affecting motile cilia lining the respiratory tract. ...The diagnostic performance of the best predictive variables was estimated by calculating sensitivity and specificity …
BACKGROUND AND OBJECTIVE: Primary ciliary dyskinesia (PCD) is a rare inherited disease affecting motile cilia lining th …
Evaluation of age at diagnosis and clinical findings of children with primary ciliary dyskinesia.
Asfuroglu P, Ramasli Gursoy T, Sismanlar Eyuboglu T, Aslan AT. Asfuroglu P, et al. Pediatr Pulmonol. 2021 Aug;56(8):2717-2723. doi: 10.1002/ppul.25533. Epub 2021 Jun 21. Pediatr Pulmonol. 2021. PMID: 34133086
OBJECTIVE: Patients with primary ciliary dyskinesia (PCD) may present with different clinical findings at different ages, and age at diagnosis may differ. ...STUDY DESIGN: All 70 patients with PCD who were followed in our pediatric pulmonology department were …
OBJECTIVE: Patients with primary ciliary dyskinesia (PCD) may present with different clinical findings at different age …
Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia.
Shoemark A, Frost E, Dixon M, Ollosson S, Kilpin K, Patel M, Scully J, Rogers AV, Mitchison HM, Bush A, Hogg C. Shoemark A, et al. Am J Respir Crit Care Med. 2017 Jul 1;196(1):94-101. doi: 10.1164/rccm.201607-1351OC. Am J Respir Crit Care Med. 2017. PMID: 28199173 Free PMC article.
RATIONALE: The standard approach to diagnosis of primary ciliary dyskinesia (PCD) in the United Kingdom consists of assessing ciliary function by high-speed microscopy and ultrastructure by election microscopy, but equipment and expertise is not widely …
RATIONALE: The standard approach to diagnosis of primary ciliary dyskinesia (PCD) in the United Kingdom consists of ass …
Lung function from school age to adulthood in primary ciliary dyskinesia.
Halbeisen FS, Pedersen ESL, Goutaki M, Spycher BD, Amirav I, Boon M, Cohen-Cymberknoh M, Crowley S, Emiralioglu N, Haarman EG, Karadag B, Koerner-Rettberg C, Latzin P, Loebinger MR, Lucas JS, Mazurek H, Morgan L, Marthin J, Pohunek P, Santamaria F, Schwerk N, Thouvenin G, Yiallouros P, Nielsen KG, Kuehni CE. Halbeisen FS, et al. Eur Respir J. 2022 Oct 20;60(4):2101918. doi: 10.1183/13993003.01918-2021. Print 2022 Oct. Eur Respir J. 2022. PMID: 35301251 Free PMC article.
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be progressive, but longitudinal data on lung function are scarce. ...FEV(1) z-scores improved over time in 21% of patients, remained stable in 40% and declined i
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be progressive, but lo
Nasal polyposis pathophysiology: Endotype and phenotype open issues.
Brescia G, Zanotti C, Parrino D, Barion U, Marioni G. Brescia G, et al. Am J Otolaryngol. 2018 Jul-Aug;39(4):441-444. doi: 10.1016/j.amjoto.2018.03.020. Epub 2018 Mar 7. Am J Otolaryngol. 2018. PMID: 29550078 Review.
On the other hand, because of their known pathophysiological mechanisms, some well-known diseases associated with aggressive forms of CRSwNP, such as eosinophilic granulomatosis with polyangiitis, primary ciliary dyskinesia and cystic fibrosis, should be inve …
On the other hand, because of their known pathophysiological mechanisms, some well-known diseases associated with aggressive forms of CRSwNP …
Management of primary ciliary dyskinesia in European children: recommendations and clinical practice.
Strippoli MP, Frischer T, Barbato A, Snijders D, Maurer E, Lucas JS, Eber E, Karadag B, Pohunek P, Zivkovic Z, Escribano A, O'Callaghan C, Bush A, Kuehni CE; ERS Task Force onPrimary Ciliary Dyskinesia in Children. Strippoli MP, et al. Eur Respir J. 2012 Jun;39(6):1482-91. doi: 10.1183/09031936.00073911. Epub 2012 Jan 26. Eur Respir J. 2012. PMID: 22282549 Free article.
The European Respiratory Society Task Force on primary ciliary dyskinesia (PCD) in children recently published recommendations for diagnosis and management. ...Overall, 90% of centres had access to nasal or bronchial mucosal biopsy. Samples were analysed by e …
The European Respiratory Society Task Force on primary ciliary dyskinesia (PCD) in children recently published recommen …
Pulmonary functions, nasal symptoms, and quality of life in patients with primary ciliary dyskinesia (PCD).
Gut G, Bar-Yoseph R, Hanna M, Brandl N, Alisha I, Rizik S, Pollak M, Hakim F, Amirav I, Bentur L, Gur M. Gut G, et al. Pediatr Pulmonol. 2024 Mar;59(3):688-694. doi: 10.1002/ppul.26814. Epub 2023 Dec 20. Pediatr Pulmonol. 2024. PMID: 38116904
BACKGROUND: Several factors may influence quality of life (QOL) for patients with primary ciliary dyskinesia (PCD). We aimed to evaluate the association between pulmonary functions, nasal symptoms and QOL in PCD patients. ...RESULTS: Twenty-seven patients (56 …
BACKGROUND: Several factors may influence quality of life (QOL) for patients with primary ciliary dyskinesia (PCD). We …
In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases.
Bukowy Z, Ziętkiewicz E, Witt M. Bukowy Z, et al. J Appl Genet. 2011 Feb;52(1):39-51. doi: 10.1007/s13353-010-0005-1. Epub 2010 Dec 2. J Appl Genet. 2011. PMID: 21125367 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic disorder caused by the impaired functioning of ciliated cells. ...The culturing of differentiated cells and tissues derived from the human RE seems to be the best way to diagnose PCD, to study genotype-phenot
Primary ciliary dyskinesia (PCD) is a rare genetic disorder caused by the impaired functioning of ciliated cells. ...Th
Comparison of mental health in individuals with primary ciliary dyskinesia, cystic fibrosis, and parent caregivers.
Graziano S, Ullmann N, Rusciano R, Allegorico A, Boldrini F, Rosito L, Quittner AL, Cutrera R, Tabarini P. Graziano S, et al. Respir Med. 2023 Feb;207:107095. doi: 10.1016/j.rmed.2022.107095. Epub 2022 Dec 23. Respir Med. 2023. PMID: 36572068
INTRODUCTION: Individuals with chronic respiratory diseases and caregivers are at higher risk for depression and anxiety. Primary ciliary dyskinesia (PCD) and cystic fibrosis (CF) are both rare genetic diseases, characterized by recurrent respiratory infectio …
INTRODUCTION: Individuals with chronic respiratory diseases and caregivers are at higher risk for depression and anxiety. Primary
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