1. Mucociliary transport in trachea of patients with cystic fibrosis;Yeates, D.B.; Sturgess, J.M.; Kahn, SR, Levison; H, Aspin; N.;Arch Dis Child,1976
2. ation of these differences. Dalhamn et al reported Camner P. Cystic fibrosis compared with immotile-cilia no difference between beat frequency in sinus and bronchial mucosa in six patients with bronchiectasis compared with four normal subjects.27 Although the slower beat frequency in our patients syndrome. A study of mucociliary clearance, ciliary ultrastructure, clinical picture and ventilatory function;Kollberg, H.; Mossberg, B.; Afzelius, B.A.; Philipson, K.;Scand J Respir Dis,1978
3. Nasal mucosa in cystic fibrosis;Magid, S.L.; Smith, C.C.; Dolowitz, D.A.;Arch Otolaryngol,1967
4. Pathology, of the lung. Third edition;Spencer, H.,1977
5. Nasal clearance in monozygotic twins;Am Rev Respir Dis,1974