The common cold [0.03%]
普通感冒
P B Van Cauwenberge,M J van Kempen,C Bachert
P B Van Cauwenberge
Upper respiratory tract infections are one of the most common infectious diseases in man and are mainly caused by rhinoviruses. A rhinoviral cold is characterized by a neutrophilic inflammatory reaction with relatively mild symptoms that ra...
Western lifestyle, local defenses and the rising incidence of allergic rhinitis [0.03%]
西方的生活方式和本土的防御体系以及过敏性鼻炎发病率的升高
J Ceuppens
J Ceuppens
Allergy was probably rare at the beginning of this century, but its prevalence in developed countries has now risen to true epidemic proportions. There has been about a doubling of children with allergic rhinitis in the past twenty years. T...
Humoral immunodeficiency in recurrent upper respiratory tract infections. Some basic, clinical and therapeutic features [0.03%]
反复呼吸道感染患者的体液免疫缺陷：一些基础、临床和治疗特点
J Daele,A F Zicot
J Daele
Adequate surface protection of the upper airway tract depends on intimate co-operation between natural non specific defence mechanisms such as ciliary function and acquired adaptative immunity. The latter is mediated by specific antibodies ...
M Proesmans,K De Boeck
M Proesmans
Cystic fibrosis (CF) is an hereditary disease with pancreatic insufficiency and chronic respiratory tract infections leading to irreversible lung damage as its main features. The typical pathogen for the respiratory disease is Pseudomonas a...
Success rates of respiratory epithelial cell culture techniques with ciliogenesis for diagnosing primary ciliary dyskinesia [0.03%]
纤毛发生呼吸道上皮细胞培养技术诊断原发性纤毛运动障碍的成功率
M Jorissen,T Willems
M Jorissen
The sequential monolayer-suspension culture technique has been used in over 800 samples during the period from January 1, 1990 till December 31, 1999. Patients were referred from all over Belgium. The culture technique was successful in 75%...
Ultrastructural expression of primary ciliary dyskinesia after ciliogenesis in culture [0.03%]
体外培养纤毛形成后的原发性纤毛运动障碍的超微结构表现
M Jorissen,T Willems,B Van der Schueren et al.
M Jorissen et al.
During the period 1990-1999 84 PCD patients were identified and characterized. The expression of inherited abnormalities in primary ciliary dyskinesia after ciliogenesis was investigated in 41 patients with dynein deficiency, 6 patients wit...
M Jorissen,T Willems,B Van der Schueren et al.
M Jorissen et al.
Ultrastructural secondary ciliary dyskinesia (SCD) was measured using transmission electron microscopy in 301 biopsies and 439 samples after ciliogenesis in the sequential monolayer-suspension culture. Biopsies were taken in the context of ...
Dynein arms and spokes after ciliogenesis in cultured respiratory epithelial cells from non-PCD individuals [0.03%]
非纤毛动力蛋白的臂和辐条在培养的呼吸上皮细胞中的纤毛发生后的结构
M Jorissen,T Willems,B Van der Schueren et al.
M Jorissen et al.
Dynein arms and spokes are crucial components of cilia. Reference values for the dynein arms and spokes were calculated based on biopsies from non-PCD patients as well as after ciliogenesis in culture. The mean values in the biopsies (n = 2...
Primary ciliary dyskinesia [0.03%]
原发性纤毛运动障碍
A Bush
A Bush
Primary ciliary dyskinesia (PCD) is an inherited condition characterised by functional and/or structural congenital abnormalities of cilia. Presentation is often in the neonatal period, but there are age-related differences in presentation,...
B Bertrand,S Collet,P Eloy et al.
B Bertrand et al.
The system of mucociliary clearance has the important task to remove from the airways inhaled substances and locally formed secretions. Inborn disorders of the mucociliary transport are due to ciliary dysfunction (Primary Ciliary Dyskinesia...