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Quoted phrase not found in phrase index: "Ciliary dyskinesia, primary, 43"
Page 1
Lung Transplantation for Primary Ciliary Dyskinesia and Kartagener Syndrome: A Multicenter Study.
Marro M, Leiva-Juárez MM, D'Ovidio F, Chan J, Van Raemdonck D, Ceulemans LJ, Moreno P, Kindelan AA, Krueger T, Koutsokera A, Ehrsam JP, Inci I, Yazicioglu A, Yekeler E, Boffini M, Brioude G, Thomas PA, Pizanis N, Aigner C, Schiavon M, Rea F, Anile M, Venuta F, Keshavjee S. Marro M, et al. Transpl Int. 2023 Feb 14;36:10819. doi: 10.3389/ti.2023.10819. eCollection 2023. Transpl Int. 2023. PMID: 36865666 Free PMC article.
Primary ciliary dyskinesia, with or without situs abnormalities, is a rare lung disease that can lead to an irreversible lung damage that may progress to respiratory failure. ...Secondary outcomes included primary graft dysfunction within 72 h and the …
Primary ciliary dyskinesia, with or without situs abnormalities, is a rare lung disease that can lead to an irreversibl …
Primary ciliary dyskinesia in Volendam: Diagnostic and phenotypic features in patients with a CCDC114 mutation.
Kos R, Israëls J, van Gogh CDL, Altenburg J, Diepenhorst S, Paff T, Boon EMJ, Micha D, Pals G, Neerincx AH, Maitland-van der Zee AH, Haarman EG; Amsterdam Mucociliary Clearance Disease (AMCD) Research Group. Kos R, et al. Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):89-101. doi: 10.1002/ajmg.c.31968. Epub 2022 Mar 27. Am J Med Genet C Semin Med Genet. 2022. PMID: 35343062 Free PMC article.
Primary ciliary dyskinesia (PCD) is a heterogeneous disease, with impaired mucociliary clearance causing respiratory tract infections. ...Only 30% of patients had situs inversus. FEV(1) declined in children (-1.43%/year, CI: -1.80/-1.05), but not in ad …
Primary ciliary dyskinesia (PCD) is a heterogeneous disease, with impaired mucociliary clearance causing respiratory tr …
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. ...RESULTS: Common clinical features incl …
OBJECTIVE: To report detailed knowledge about the clinical manifestations, ciliary phenotypes, genetic spectrum as well as phenotype/ …
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype.
Kinghorn B, Rosenfeld M, Sullivan E, Onchiri F, Ferkol TW, Sagel SD, Dell SD, Milla C, Shapiro AJ, Sullivan KM, Zariwala MA, Pittman JE, Mollica F, Tiddens HAWM, Kemner-van de Corput M, Knowles MR, Davis SD, Leigh MW. Kinghorn B, et al. Ann Am Thorac Soc. 2023 Apr;20(4):539-547. doi: 10.1513/AnnalsATS.202206-524OC. Ann Am Thorac Soc. 2023. PMID: 36442147 Free PMC article.
Rationale: Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance, recurrent respiratory infections, progressive airway damage, and obstructive lung disease. ...Objectives: We sought to delineate the association of ciliary …
Rationale: Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance, recurrent respiratory i …
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 …
Analysis of the clinical features of Japanese patients with primary ciliary dyskinesia.
Chiyonobu K, Xu Y, Feng G, Saso S, Ogawa S, Ikejiri M, Abo M, Kondo M, Gotoh S, Kubo H, Hosoki K, Nagao M, Fujisawa T, Nakatani K, Takeuchi K. Chiyonobu K, et al. Auris Nasus Larynx. 2022 Apr;49(2):248-257. doi: 10.1016/j.anl.2021.08.003. Epub 2021 Aug 26. Auris Nasus Larynx. 2022. PMID: 34454779 Free article.
OBJECTIVE: Primary ciliary dyskinesia (PCD) is a rare hereditary disease. Most reports of PCD in Japan are case reports, and clinical analysis has not been performed. ...Data on the following items were collected and analyzed: age at first visit to the hospit …
OBJECTIVE: Primary ciliary dyskinesia (PCD) is a rare hereditary disease. Most reports of PCD in Japan are case reports …
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. ...This …
Cystic fibrosis (CF) causes significant caregiver burden, but the current data is scarce. In the case of primary ciliary dy …
Clinical and genetic features of primary ciliary dyskinesia in a cohort of consecutive clinically suspect children in western China.
Li Y, Fu W, Geng G, Dai J, Fu Z, Tian D. Li Y, et al. BMC Pediatr. 2022 Jul 8;22(1):402. doi: 10.1186/s12887-022-03469-x. BMC Pediatr. 2022. PMID: 35804324 Free PMC article.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, inherited disorder of the motile cilia that exhibits genetic and clinical heterogeneity among different populations. ...All patients presented with a chronic wet cough, 93.75% exhibited chronic or recurr …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, inherited disorder of the motile cilia that exhibits genetic an …
Etiology and clinical characteristics of a non-cystic fibrosis bronchiectasis cohort in a middle eastern population.
Shafiq I, Wahla AS, Uzbeck MH, Zoumot Z, Abuzakouk M, Elkhalifa S, Bodi G, Almazrouei KM, Bodi K, Isse S. Shafiq I, et al. BMC Pulm Med. 2023 Jul 10;23(1):250. doi: 10.1186/s12890-023-02543-z. BMC Pulm Med. 2023. PMID: 37430275 Free PMC article.
RESULTS: In total we analysed 260 records (63% female, 37% male), with median age of 58 years (interquartile range (IQR) 38-71), Body Mass Index (BMI) 25.8(IQR 22-30), forced expiratory volume in the first second (FEV1) %predicted 65 (IQR 43-79) and FEV1/forced vital capac …
RESULTS: In total we analysed 260 records (63% female, 37% male), with median age of 58 years (interquartile range (IQR) 38-71), Body Mass I …
Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients.
Dell SD, Leigh MW, Lucas JS, Ferkol TW, Knowles MR, Alpern A, Behan L, Morris AM, Hogg C, DunnGalvin A, Quittner AL. Dell SD, et al. Ann Am Thorac Soc. 2016 Oct;13(10):1726-1735. doi: 10.1513/AnnalsATS.201603-198OC. Ann Am Thorac Soc. 2016. PMID: 27464304 Free PMC article.
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disease. There are no available data on disease-specific pediatric patient-reported outcomes. ...Various items were retained in questionnaires, based on age and role of respondent: 37, 43, and 41 it …
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disease. There are no available data on disease-specific pediatri …
33 results