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Quoted phrase not found in phrase index: "Primary ciliary dyskinesia 21"
Page 1
Primary ciliary dyskinesia.
Lobo LJ, Zariwala MA, Noone PG. Lobo LJ, et al. QJM. 2014 Sep;107(9):691-9. doi: 10.1093/qjmed/hcu063. Epub 2014 Mar 19. QJM. 2014. PMID: 24652656 Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function, leading to chronic infections of the respiratory tract, fertility problems and disorders of organ laterality. ...There are 21 known PCD causing …
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function, leading to chronic …
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. ...Larger, longer clinical studies are warranted to explore the p …
BACKGROUND: Mucociliary clearance is dysfunctional in people with primary ciliary dyskinesia, resulting in the accumula …
Nasal nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and healthy children.
Güney E, Emiralioğlu N, Cinel G, Yalçın E, Doğru D, Kiper N, Özçelik HU. Güney E, et al. Turk J Pediatr. 2019;61(1):20-25. doi: 10.24953/turkjped.2019.01.004. Turk J Pediatr. 2019. PMID: 31559717 Free article. Clinical Trial.
Guney E, Emiralioglu N, Cinel G, Yalcin E, Dogru D, Kiper N, Ozcelik HU. Nasal nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and healthy children. Turk J Pediatr 2019; 61: 20-25. Primary ciliary dyskinesia (PCD) is a …
Guney E, Emiralioglu N, Cinel G, Yalcin E, Dogru D, Kiper N, Ozcelik HU. Nasal nitric oxide levels in primary ciliary dyski …
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects.
Frommer A, Hjeij R, Loges NT, Edelbusch C, Jahnke C, Raidt J, Werner C, Wallmeier J, Große-Onnebrink J, Olbrich H, Cindrić S, Jaspers M, Boon M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Marthin JK, Nielsen KG, Amirav I, Elias N, Kerem E, Shoseyov D, Haeffner K, Omran H. Frommer A, et al. Am J Respir Cell Mol Biol. 2015 Oct;53(4):563-73. doi: 10.1165/rcmb.2014-0483OC. Am J Respir Cell Mol Biol. 2015. PMID: 25789548 Free PMC article.
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several distinct defects in genes responsible for ciliary beating, leading to defective mucociliary clearance often associated with randomization of lef …
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several distinct defects i …
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. ...For the non-Jewish (mainly Druze and Arab Moslem) compared to Jewish populations, prevalence was 1:16,500 and 1:139,000 respectively (p < 0.0001) an

…
BACKGROUND: Primary Ciliary Dyskinesia (PCD) is rare and its features in Israel have not been described. ...For the non …
Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.
Leigh MW, Ferkol TW, Davis SD, Lee HS, Rosenfeld M, Dell SD, Sagel SD, Milla C, Olivier KN, Sullivan KM, Zariwala MA, Pittman JE, Shapiro AJ, Carson JL, Krischer J, Hazucha MJ, Knowles MR. Leigh MW, et al. Ann Am Thorac Soc. 2016 Aug;13(8):1305-13. doi: 10.1513/AnnalsATS.201511-748OC. Ann Am Thorac Soc. 2016. PMID: 27070726 Free PMC article.
RATIONALE: Primary ciliary dyskinesia (PCD), a genetically heterogeneous, recessive disorder of motile cilia, is associated with distinct clinical features. ...Clinical trial registered with ClinicalTrials.gov (NCT00323167)....
RATIONALE: Primary ciliary dyskinesia (PCD), a genetically heterogeneous, recessive disorder of motile cilia, is associ …
Ciliary disorientation alone as a cause of primary ciliary dyskinesia syndrome.
Rayner CF, Rutman A, Dewar A, Greenstone MA, Cole PJ, Wilson R. Rayner CF, et al. Am J Respir Crit Care Med. 1996 Mar;153(3):1123-9. doi: 10.1164/ajrccm.153.3.8630555. Am J Respir Crit Care Med. 1996. PMID: 8630555
Ciliary disorientation has been proposed as a variant of primary ciliary dyskinesia (PCD); cilia have normal ultrastructure and normal or near normal ciliary beat frequency (CBF) but lack efficacy because their beat direction is disorientated. . …
Ciliary disorientation has been proposed as a variant of primary ciliary dyskinesia (PCD); cilia have normal ult …
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 …
Pulmonary radioaerosol mucociliary clearance in diagnosis of primary ciliary dyskinesia.
Marthin JK, Mortensen J, Pressler T, Nielsen KG. Marthin JK, et al. Chest. 2007 Sep;132(3):966-76. doi: 10.1378/chest.06-2951. Epub 2007 Jul 23. Chest. 2007. PMID: 17646235 Clinical Trial.
BACKGROUND: Methods relying on nasal ciliary motility for the diagnosis of primary ciliary dyskinesia (PCD) are often hampered by secondary ciliary dyskinesia. ...PRMC was studied after (99m)Tc-albumin colloid aerosol inhalation, a …
BACKGROUND: Methods relying on nasal ciliary motility for the diagnosis of primary ciliary dyskinesia (PC …
NMR Profiling of Exhaled Breath Condensate Defines Different Metabolic Phenotypes of Non-Cystic Fibrosis Bronchiectasis.
Paris D, Palomba L, Mirra V, Borrelli M, Corcione A, Santamaria F, Maniscalco M, Motta A. Paris D, et al. Int J Mol Sci. 2020 Nov 14;21(22):8600. doi: 10.3390/ijms21228600. Int J Mol Sci. 2020. PMID: 33202684 Free PMC article. Clinical Trial.
We evaluated whether NMR-based metabolomics discriminates the EBC-derived metabolic phenotypes ("metabotypes") of 41 patients with non-cystic fibrosis (nCF) bronchiectasis of various etiology [24 subjects with Primary Ciliary Dyskinesia (PCD); 17 patients wit …
We evaluated whether NMR-based metabolomics discriminates the EBC-derived metabolic phenotypes ("metabotypes") of 41 patients with non-cysti …
30 results