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Quoted phrase not found in phrase index: "Ciliary dyskinesia, primary, 51"
Page 1
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practices.
Abitbul R, Amirav I, Blau H, Alkrinawi S, Aviram M, Shoseyov D, Bentur L, Avital A, Springer C, Lavie M, Prais D, Dabbah H, Elias N, Elizur A, Goldberg S, Hevroni A, Kerem E, Luder A, Roth Y, Cohen-Cymberknoh M, Ben Ami M, Mandelberg A, Livnat G, Picard E, Rivlin J, Rotschild M, Soferman R, Loges NT, Olbrich H, Werner C, Wolter A, Herting M, Wallmeier J, Raidt J, Omran H, Mussaffi H. Abitbul R, et al. Respir Med. 2016 Oct;119:41-47. doi: 10.1016/j.rmed.2016.08.015. Epub 2016 Aug 23. Respir Med. 2016. PMID: 27692146 Free article. Clinical Trial.
BACKGROUND: Primary Ciliary Dyskinesia (PCD) is rare and its features in Israel have not been described. ...Diagnostic verification revealed for 150 PCD patients: 81% nNO<233 ppb, 62% abnormal HVMA, 51% diagnostic TEM, 58% diagnostic IF and, 57% gen …
BACKGROUND: Primary Ciliary Dyskinesia (PCD) is rare and its features in Israel have not been described. ...Diagnostic …
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.
Shapiro AJ, Zariwala MA, Ferkol T, Davis SD, Sagel SD, Dell SD, Rosenfeld M, Olivier KN, Milla C, Daniel SJ, Kimple AJ, Manion M, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium. Shapiro AJ, et al. Pediatr Pulmonol. 2016 Feb;51(2):115-32. doi: 10.1002/ppul.23304. Epub 2015 Sep 29. Pediatr Pulmonol. 2016. PMID: 26418604 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung disease resulting in chronic oto-sino-pulmonary disease in both children and adults. ...These recommendations have been adopted by the governing board of the PCD Foundation to provide …
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung disease resulting in chronic oto-sino-pulmon …
Variation in treatment strategies for the eradication of Pseudomonas aeruginosa in primary ciliary dyskinesia across European centers.
Crowley S, Holgersen MG, Nielsen KG. Crowley S, et al. Chron Respir Dis. 2019 Jan-Dec;16:1479972318787919. doi: 10.1177/1479972318787919. Epub 2018 Jul 18. Chron Respir Dis. 2019. PMID: 30021461 Free PMC article.
Primary ciliary dyskinesia (PCD) is a rare disease causing motile cilia dysfunction, recurrent airway infection, and bronchiectasis. ...Few centers had written guidelines for PCD management. Clinical trials to determine optimal treatment of PA in PCD p …
Primary ciliary dyskinesia (PCD) is a rare disease causing motile cilia dysfunction, recurrent airway infection, and br …
A longitudinal evaluation of hearing and ventilation tube insertion in patients with primary ciliary dyskinesia.
Andersen TN, Alanin MC, von Buchwald C, Nielsen LH. Andersen TN, et al. Int J Pediatr Otorhinolaryngol. 2016 Oct;89:164-8. doi: 10.1016/j.ijporl.2016.08.011. Epub 2016 Aug 18. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27619050
INTRODUCTION: Primary ciliary dyskinesia (PCD) is an autosomal recessive genetic disease, which primarily manifests with oto-sino-pulmonary symptoms. ...
INTRODUCTION: Primary ciliary dyskinesia (PCD) is an autosomal recessive genetic disease, which primarily manifests wit …
CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia.
Liu L, Zhou K, Song Y, Liu X. Liu L, et al. Medicine (Baltimore). 2021 Dec 23;100(51):e28275. doi: 10.1097/MD.0000000000028275. Medicine (Baltimore). 2021. PMID: 34941110 Free PMC article.
TRIAL DESIGN: Primary ciliary dyskinesia (PCD) is a genetical disease that inherited in an autosomal-recessive way. Its clinical manifestations (such as male infertility) are mainly caused by defects of motion-related cilia that encoded by mutat …
TRIAL DESIGN: Primary ciliary dyskinesia (PCD) is a genetical disease that inherited in an autosomal-recessive w …
Two cases of primary ciliary dyskinesia with different responses to macrolide treatment.
Kido T, Yatera K, Yamasaki K, Nagata S, Choujin Y, Yamaga C, Hara K, Ishimoto H, Hisaoka M, Mukae H. Kido T, et al. Intern Med. 2012;51(9):1093-8. doi: 10.2169/internalmedicine.51.6617. Epub 2012 Apr 29. Intern Med. 2012. PMID: 22576394 Free article. Review.
We herein report two cases of primary ciliary dyskinesia (PCD) with different responses to macrolides. ...
We herein report two cases of primary ciliary dyskinesia (PCD) with different responses to macrolides. ...
Recovery of baseline lung function after pulmonary exacerbation in children with primary ciliary dyskinesia.
Sunther M, Bush A, Hogg C, McCann L, Carr SB. Sunther M, et al. Pediatr Pulmonol. 2016 Dec;51(12):1362-1366. doi: 10.1002/ppul.23479. Epub 2016 Jun 8. Pediatr Pulmonol. 2016. PMID: 27273679 Free article.
RATIONALE: Spirometry in children with cystic fibrosis (CF) frequently fails to return to baseline after treatment for a pulmonary exacerbation. It is unclear whether the same is true for children with primary ciliary dyskinesia (PCD). OBJECTIVES: To determin …
RATIONALE: Spirometry in children with cystic fibrosis (CF) frequently fails to return to baseline after treatment for a pulmonary exacerbat …
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene.
Omran H, Häffner K, Völkel A, Kuehr J, Ketelsen UP, Ross UH, Konietzko N, Wienker T, Brandis M, Hildebrandt F. Omran H, et al. Am J Respir Cell Mol Biol. 2000 Nov;23(5):696-702. doi: 10.1165/ajrcmb.23.5.4257. Am J Respir Cell Mol Biol. 2000. PMID: 11062149
Reduced mucociliary clearance in primary ciliary dyskinesia (PCD) causes recurrent infections of the upper and lower respiratory tract. ...Two of four affected individuals exhibited a situs inversus, typical for Kartagener syndrome, due to randomization …
Reduced mucociliary clearance in primary ciliary dyskinesia (PCD) causes recurrent infections of the upper and lower re …
Clinical reminders attached to echocardiography reports of patients with reduced left ventricular ejection fraction increase use of beta-blockers: a randomized trial.
Heidenreich PA, Gholami P, Sahay A, Massie B, Goldstein MK. Heidenreich PA, et al. Circulation. 2007 Jun 5;115(22):2829-34. doi: 10.1161/CIRCULATIONAHA.106.684753. Epub 2007 May 21. Circulation. 2007. PMID: 17515459 Clinical Trial.
The primary outcome was a prescription for an oral beta-blocker between 1 and 9 months after randomization. ...More patients randomized to the reminder had a subsequent beta-blocker prescription (74%, 458 of 621) compared with those randomized to no re …
The primary outcome was a prescription for an oral beta-blocker between 1 and 9 months after randomization. ...More patients …