Results 211 to 220 of about 16,014 (252)

Asthma Among Children With Primary Ciliary Dyskinesia.

JAMA Netw Open
Zein J, Owora A, Kim HJ, Marozkina N, Gaston B.   +4 more
europepmc   +1 more source

How well does spirometry capture the symptom range in primary ciliary dyskinesia? – a cross-sectional national study

Lam YT, Koller M, Schreck LD, Clarenbach C, Jung A, Kieninger E, Kuehni CE, Goutaki M.   +7 more
europepmc   +1 more source

Characterisation of primary ciliary dyskinesia model generated from BMI1 transduced basal epithelial cells

Dalbay, Melis T, Shahaj, Eriomina, Guerrini, Ileana, Lee, Dani Do Hyang, Straatman-Iwanowska, Anna, Mitchison, Hannah M, Baines, Deborah L, Hirst, Robert A, Hogg, Claire, O'Callaghan, Christopher, Hart, Stephen L   +10 more
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Primary Ciliary Dyskinesia

Seminars in Respiratory and Critical Care Medicine, 2021
AbstractPrimary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. The estimated PCD prevalence in children with bronchiectasis is up to 26% and in adults with bronchiectasis is 1 to 13%. Due to dysfunction of the multiple motile cilia of the respiratory tract patients suffer from poor mucociliary clearance.
Shoemark, Amelia, Harman, Katharine
openaire   +3 more sources

Primary Ciliary Dyskinesia: Ciliary Activity

Acta Oto-Laryngologica, 1986
In primary ciliary dyskinesia (PCD) the cilia of the respiratory tract are immotile or they show an incoordinate, abnormal beating pattern. Consequently, mucociliary clearance is lacking. Most patients with PCD have ultrastructural abnormalities in their cilia. In some patients, however, the ciliary ultrastructure is completely normal.
van der Baan, S., Veerman, A. J., Wulffraat, N., Bezemer, P. D., Feenstra, L.   +4 more
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Primary ciliary dyskinesia. Ciliopathies

Acta Otorrinolaringologica (English Edition), 2010
Primary ciliary dyskinesia is a genetically inherited syndrome characterized by cilia immotility or dysmotility. Deficiency in mucociliary clearance produces chronic respiratory infections since birth, male sterility by spermatozoid immotility and situs inversus in 40-50% of patients (Kartagener's syndrome).
Miguel, Armengot Carceller, Manuel, Mata Roig, Xavier, Milara Payá, Julio, Cortijo Gimeno   +3 more
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Primary Ciliary Dyskinesia

Pediatrics In Review, 2017
1. Rebecca Butterfield, MD* 1. *Albany Medical Center, Albany, NY 1. 1. Stillwell PC, 2. Wartchow EP, 3. Sagel SD Primary Ciliary Dyskinesia in Children: A Review for Pediatricians, Allergists, and Pediatric Pulmonologists. Stillwell PC, Wartchow EP, Sagel SD. Pediatr Allergy Immunol Pulmonol.
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Primary ciliary dyskinesia (PCD)

Pediatric Pulmonology, 2000
This article summarizes the current state of the scientific and clinical knowledge that relates to primary ciliary dyskinesia (PCD). Although PCD is a rare disease with a prevalence of 1 in 20,000 it has a well recognized morbidity. It is believed that an accurate diagnosis and the application of appropriate management can significantly reduce this ...
M, Meeks, A, Bush
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Primary Ciliary Dyskinesia

Seminars in Respiratory and Critical Care Medicine, 2003
Primary ciliary dyskinesia (PCD) is an inherited disorder characterized by impaired ciliary function that leads to an array of clinical manifestations including chronic bronchitis, chronic sinusitis, chronic otitis media, situs inversus (in approximately 50% of cases), and infertility. The underlying genetic and molecular defects have not been defined.
openaire   +2 more sources