نتایج جستجو برای: primary ciliary dyskinesia
تعداد نتایج: 653356 فیلتر نتایج به سال:
Primary ciliary dyskinesia (PCD) is a rare hereditary disease from the group of ciliopathies, which based on defect in cilia ultrastructure respiratory epithelium and similar structures (sperm flagella, villi fallopian tubes, ventricular ependyma, etc.), leading to motor function impairment. The prevalence varies significantly around world not known reliably Russian Federation. aim review was a...
No study has evaluated the correlation between different expression of nitric oxide synthase (NOS) isoforms in nasal epithelial cells and nasal NO (nNO) level in primary ciliary dyskinesia (PCD). Gene expression of endothelial (NOS3) and inducible NOS (NOS2) and their correlation with nNO level, ciliary function and morphology were studied in patients with PCD or secondary ciliary dyskinesia (S...
One hundred and sixty seven children, ranging in age from 5 weeks to 16 years, with chronic upper or lower respiratory tract problems, or both, were investigated for ciliary dyskinesia. Abnormal ciliary function was found in 18 cases all of whom had chronic lower respiratory disease and most of whom also had upper respiratory problems. Fifteen of the 18 cases had reduced ciliary beat frequencie...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید