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Quoted phrase not found in phrase index: "Primary ciliary dyskinesia 13"
Page 1
Sinus Development and Pneumatization in a Primary Ciliary Dyskinesia Cohort.
Pappa AK, Sullivan KM, Lopez EM, Adams KN, Zanation AM, Ebert CS Jr, Thorp BD, Senior BA, Leigh MW, Knowles MR, Kimple AJ. Pappa AK, et al. Am J Rhinol Allergy. 2021 Jan;35(1):72-76. doi: 10.1177/1945892420933175. Epub 2020 Jun 19. Am J Rhinol Allergy. 2021. PMID: 32551925 Free PMC article.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a genetically diverse disease which causes impaired mucociliary clearance, and results in pulmonary, otologic, and rhinologic disease in affected patients. ...A control population of patients who had preoperativ …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a genetically diverse disease which causes impaired mucociliary clearan …
Clinical and Genetic Spectrum of Children with Primary Ciliary Dyskinesia in China.
Guo Z, Chen W, Wang L, Qian L. Guo Z, et al. J Pediatr. 2020 Oct;225:157-165.e5. doi: 10.1016/j.jpeds.2020.05.052. Epub 2020 Jun 2. J Pediatr. 2020. PMID: 32502479
OBJECTIVE: To report detailed knowledge about the clinical manifestations, ciliary phenotypes, genetic spectrum as well as phenotype/genotype correlation in primary ciliary dyskinesia (PCD) in Chinese children. ...Overall, ciliary ultrastructura …
OBJECTIVE: To report detailed knowledge about the clinical manifestations, ciliary phenotypes, genetic spectrum as well as phenotype/ …
Nasal versus tracheobronchial biopsies to diagnose primary ciliary dyskinesia: A meta-analysis.
Adil EA, Kawai K, Dombrowski N, Irace AL, Cunningham MJ. Adil EA, et al. Laryngoscope. 2017 Jan;127(1):6-13. doi: 10.1002/lary.26070. Epub 2016 Jun 16. Laryngoscope. 2017. PMID: 27312809 Review.
OBJECTIVES/HYPOTHESIS: To systematically review the literature regarding the efficacy of different biopsy sites and methods to obtain an adequate ciliary sample for ultrastructural examination with electron microscopy (EM) for the diagnosis of primary ciliary …
OBJECTIVES/HYPOTHESIS: To systematically review the literature regarding the efficacy of different biopsy sites and methods to obtain an ade …
Picking up speed: advances in the genetics of primary ciliary dyskinesia.
Horani A, Brody SL, Ferkol TW. Horani A, et al. Pediatr Res. 2014 Jan;75(1-2):158-64. doi: 10.1038/pr.2013.200. Epub 2013 Nov 5. Pediatr Res. 2014. PMID: 24192704 Free PMC article. Review.
Abnormal ciliary axonemal structure and function are linked to the growing class of genetic disorders collectively known as ciliopathies, and our understanding of the complex genetics and functional phenotypes of these conditions has rapidly expanded. While progress …
Abnormal ciliary axonemal structure and function are linked to the growing class of genetic disorders collectively known as ci …
Clinical characteristics and genetic spectrum of 26 individuals of Chinese origin with primary ciliary dyskinesia.
Zhao X, Bian C, Liu K, Xu W, Liu Y, Tian X, Bai J, Xu KF, Zhang X. Zhao X, et al. Orphanet J Rare Dis. 2021 Jul 1;16(1):293. doi: 10.1186/s13023-021-01840-2. Orphanet J Rare Dis. 2021. PMID: 34210339 Free PMC article.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, highly heterogeneous genetic disorder involving the impairment of motile cilia. ...RESULTS: A total of 26 individuals of Chinese origin with a confirmed PCD diagnosis aged 13 to 61 years (median a …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, highly heterogeneous genetic disorder involving the impairment …
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 …
CT imaging features of paranasal sinuses in children with primary ciliary dyskinesia.
Lyu H, Guo Z, Chen C, Duan B, Xu Z, Chen W. Lyu H, et al. Acta Otolaryngol. 2022 Sep-Dec;142(9-12):691-695. doi: 10.1080/00016489.2022.2118371. Epub 2022 Sep 10. Acta Otolaryngol. 2022. PMID: 36093609
BACKGROUND: Primary ciliary dyskinesia (PCD) causes impaired mucociliary clearance and results in chronic pulmonary and sinonasal symptoms. OBJECTIVES: To study the CT imaging features of paranasal sinuses in children with PCD. MATERIALS AND METHODS: 17 PCD p …
BACKGROUND: Primary ciliary dyskinesia (PCD) causes impaired mucociliary clearance and results in chronic pulmonary and …
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia.
Blanchon S, Legendre M, Bottier M, Tamalet A, Montantin G, Collot N, Faucon C, Dastot F, Copin B, Clement A, Filoche M, Coste A, Amselem S, Escudier E, Papon JF, Louis B. Blanchon S, et al. J Med Genet. 2020 Apr;57(4):237-244. doi: 10.1136/jmedgenet-2019-106424. Epub 2019 Nov 26. J Med Genet. 2020. PMID: 31772028
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder resulting in abnormal ciliary motility/structure, extremely heterogeneous at genetic and ultrastructural levels. ...Combined outer/inner dynein arms (ODA/IDA) defect induces …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder resulting in abnormal ciliary motilit …
Evaluation of otorhinolaryngological manifestations in patients with primary ciliary dyskinesia.
Günaydın RÖ, Eroğlu E, Tellioğlu B, Emiralioğlu N, Özçelik HU, Yalçın E, Doğru D, Kiper EN. Günaydın RÖ, et al. Int J Pediatr Otorhinolaryngol. 2023 May;168:111520. doi: 10.1016/j.ijporl.2023.111520. Epub 2023 Mar 22. Int J Pediatr Otorhinolaryngol. 2023. PMID: 36990030
OBJECTIVES: Primary ciliary dyskinesia (PCD) is a genetic disease characterized by congenital impairment of mucociliary clearance causing recurrent respiratory tract infections. ...The most common ENT manifestation was otitis media with effusion (OME) (66.1%, …
OBJECTIVES: Primary ciliary dyskinesia (PCD) is a genetic disease characterized by congenital impairment of mucociliary …
Caregiver burden in children with cystic fibrosis and primary ciliary dyskinesia.
Keniş Coşkun Ö, Gençer Atalay K, Erdem E, Karadag-Saygi E, Gökdemir Y, Karadağ B. Keniş Coşkun Ö, et al. Pediatr Pulmonol. 2019 Dec;54(12):1936-1940. doi: 10.1002/ppul.24503. Epub 2019 Aug 29. Pediatr Pulmonol. 2019. PMID: 31468736
Cystic fibrosis (CF) causes significant caregiver burden, but the current data is scarce. In the case of primary ciliary dyskinesia (PCD), even less is known. This study aims to compare the caregiver burden of the parents of patients with CF and PCD. METHODS: …
Cystic fibrosis (CF) causes significant caregiver burden, but the current data is scarce. In the case of primary ciliary dy …
92 results