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Quoted phrase not found in phrase index: "Ciliary dyskinesia, primary, 37"
Page 1
Primary Ciliary Dyskinesia.
Knowles MR, Zariwala M, Leigh M. Knowles MR, et al. Clin Chest Med. 2016 Sep;37(3):449-61. doi: 10.1016/j.ccm.2016.04.008. Epub 2016 Jun 30. Clin Chest Med. 2016. PMID: 27514592 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a recessive genetically heterogeneous disorder of motile cilia with chronic otosinopulmonary disease and organ laterality defects in 50% of cases. ...
Primary ciliary dyskinesia (PCD) is a recessive genetically heterogeneous disorder of motile cilia with chronic otosino …
Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trial.
Ringshausen FC, Shapiro AJ, Nielsen KG, Mazurek H, Pifferi M, Donn KH, van der Eerden MM, Loebinger MR, Zariwala MA, Leigh MW, Knowles MR, Ferkol TW; CLEAN-PCD investigators and study team. Ringshausen FC, et al. Lancet Respir Med. 2024 Jan;12(1):21-33. doi: 10.1016/S2213-2600(23)00226-6. Epub 2023 Aug 31. Lancet Respir Med. 2024. PMID: 37660715 Clinical Trial.
BACKGROUND: Mucociliary clearance is dysfunctional in people with primary ciliary dyskinesia, resulting in the accumulation of dehydrated mucus in the airways that is difficult to clear. ...INTERPRETATION: In this phase 2 crossover study, idrevloride in hyper …
BACKGROUND: Mucociliary clearance is dysfunctional in people with primary ciliary dyskinesia, resulting in the accumula …
When to suspect primary ciliary dyskinesia in children.
Fitzgerald DA, Shapiro AJ. Fitzgerald DA, et al. Paediatr Respir Rev. 2016 Mar;18:3-7. doi: 10.1016/j.prrv.2015.11.006. Epub 2015 Nov 23. Paediatr Respir Rev. 2016. PMID: 26822945 Review.
Primary ciliary dyskinesia [PCD] is an uncommon, autosomal recessively inherited condition that is often overlooked and undertreated in childhood. ...
Primary ciliary dyskinesia [PCD] is an uncommon, autosomal recessively inherited condition that is often overlooked and …
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 …
Challenges in Diagnosing Primary Ciliary Dyskinesia in a Brazilian Tertiary Hospital.
Toro MDC, Ribeiro JD, Marson FAL, Ortiz É, Toro AADC, Bertuzzo CS, Jones MH, Sakano E. Toro MDC, et al. Genes (Basel). 2022 Jul 15;13(7):1252. doi: 10.3390/genes13071252. Genes (Basel). 2022. PMID: 35886035 Free PMC article.
Primary ciliary dyskinesia (PCD) causes cellular cilia motility alterations, leading to clinical manifestations in the upper and lower respiratory tract and situs abnormalities. ...Those patients were classified according to the degree of suspicion for …
Primary ciliary dyskinesia (PCD) causes cellular cilia motility alterations, leading to clinical manifestations …
Transmission electron microscopy study of suspected primary ciliary dyskinesia patients.
Rezaei M, Soheili A, Ziai SA, Fakharian A, Toreyhi H, Pourabdollah M, Ghorbani J, Karimi-Galougahi M, Mahdaviani SA, Hasanzad M, Eslaminejad A, Ghaffaripour HA, Mahmoudian S, Rodafshani Z, Mirenayat MS, Varahram M, Marjani M, Tabarsi P, Mansouri D, Jamaati HR, Velayati AA. Rezaei M, et al. Sci Rep. 2022 Feb 11;12(1):2375. doi: 10.1038/s41598-022-06370-w. Sci Rep. 2022. PMID: 35149751 Free PMC article.
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive condition often presenting with chronic respiratory infections in early life. ...The most common presentations were bronchiectasis: 26 (38.8%), chronic sinusitis: 23 (34.3%), and recurrent lower r …
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive condition often presenting with chronic respiratory infe …
Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.
Storm van's Gravesande K, Omran H. Storm van's Gravesande K, et al. Ann Med. 2005;37(6):439-49. doi: 10.1080/07853890510011985. Ann Med. 2005. PMID: 16203616 Review.
Primary ciliary dyskinesia (PCD) is a phenotypically and genetically heterogeneous disorder with an autosomal-recessive inheritance pattern. ...Establishment of diagnosis currently relies on electron microscopy, direct evaluation of ciliary beat by lig …
Primary ciliary dyskinesia (PCD) is a phenotypically and genetically heterogeneous disorder with an autosomal-recessive …
PRO: Primary Ciliary Dyskinesia: Genes are all you need!
Shirlow R, Fitzgerald DA. Shirlow R, et al. Paediatr Respir Rev. 2021 Mar;37:32-33. doi: 10.1016/j.prrv.2020.04.005. Epub 2020 Apr 14. Paediatr Respir Rev. 2021. PMID: 32653464 Review. No abstract available.
Going beyond the chest X-ray: Investigating laterality defects in primary ciliary dyskinesia.
Wee WB, Kaspy KR, Sawras MG, Knowles MR, Zariwala MA, Leigh MW, Dell SD, Shapiro AJ. Wee WB, et al. Pediatr Pulmonol. 2022 May;57(5):1318-1324. doi: 10.1002/ppul.25853. Epub 2022 Feb 21. Pediatr Pulmonol. 2022. PMID: 35122416 Free PMC article.
BACKGROUND: Organ laterality defects in primary ciliary dyskinesia (PCD) are common, ranging from complete mirror image organ arrangement, situs inversus totalis (SIT), to situs ambiguus (SA), which falls along the spectrum of situs solitus (SS) and SIT. ...T …
BACKGROUND: Organ laterality defects in primary ciliary dyskinesia (PCD) are common, ranging from complete mirror image …
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