Les manifestations respiratoires de la mucoviscidose
Tài liệu tham khảo
Becker, 1996, Prevalence of ABPA and atopy in adult patients with cystic fibrosis, Chest, 109, 1536, 10.1378/chest.109.6.1536
Chemery, 2004, Capacité du transfert du monoxyde de carbone (TLCO) et saturation arterielle à l'exercice chez les patients atteints de mucoviscidose, Arch. Pediatr., 11, 1060, 10.1016/j.arcped.2004.04.019
Corey, 1997, Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis, J. Pediatr., 131, 809, 10.1016/S0022-3476(97)70025-8
Counil, 2007, Mucoviscidose: du bonusage des explorations fonctionnelles respiratoires, Rev. Mal. Respir., 24, 691, 10.1016/S0761-8425(07)91145-6
Drumm, 2005, Gene modifer study group, Genetic modifiers of lung disease in cystic fibrosis, N. Engl. J. Med., 353, 1443, 10.1056/NEJMoa051469
Fauroux, 2004, Setting of non-invasive pressure support in young patients with cystic fibrosis, Eur. Respir. J., 24, 624, 10.1183/09031936.04.0000137603
Flume, 2005, Pneumothorax in cystic fibrosis, Chest, 128, 720, 10.1378/chest.128.2.720
Flume, 2005, Massive hemoptysis in cystic fibrosis, Chest, 128, 729, 10.1378/chest.128.2.729
Gulmans, 1996, The six-minute walking test in children with cystic fibrosis: reliability and validity, Pediatr. Pulmonol, 22, 85, 10.1002/(SICI)1099-0496(199608)22:2<85::AID-PPUL1>3.0.CO;2-I
Henry, 1992, Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis, Pediatr. Pulmonol, 12, 158, 10.1002/ppul.1950120306
Kerem, 1992, Prediction of mortality in patients with cystic fibrosis, N. Engl. J. Med, 326, 1187, 10.1056/NEJM199204303261804
Khan, 1995, Early pulmonary inflammation in infants with cystic fibrosis, Am. J. Respir. Crit. Care Meal, 151, 1075
Konstan, 2007, Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis, J. Pediatr, 151, 134, 10.1016/j.jpeds.2007.03.006
Lipuma, 2005, Update on the Burkholderia cepacia complex, Curr. Opin. Pulm. Med, 11, 528, 10.1097/01.mcp.0000181475.85187.ed
Mastella, 2000, Allergic bronchopulmonary aspergillosis in cystic fibrosis, A European epidemiological study, Epidemiologic registery of cystic fibrosis, Eur. Respir. J, 16, 464, 10.1034/j.1399-3003.2000.016003464.x
Nielsen, 2004, Serial lung function and responsiveness in cystic fibrosis during early childhood, Am. J. Respir. Crit. Care Med, 169, 1209, 10.1164/rccm.200303-347OC
2007, Rapport sur la situation de la mucoviscidose en France en 2005, Paris: Vaincre la mucoviscidose et Institut national d'études démographiques
Puchelle, 2002, Airway mucus in cystic fibrosis, Paediatr. Respir. Rev, 3, 115, 10.1016/S1526-0550(02)00005-7
Ramsey, 1996, Management of pulmonary disease in patients with cystic fibrosis, N. Engl. J. Med, 335, 179, 10.1056/NEJM199607183350307
Rosenberg, 1992, Spirometry and chest roentgenographic appearance in adults with cystic fibrosis, Chest, 101, 961, 10.1378/chest.101.4.961
Selvadurai, 2003, Validation of shuttle tests in children with cystic fibrosis, Pediatr. Pulmonol, 35, 133, 10.1002/ppul.10197
Schidlow, 1993, Cystic fibrosis foundation consensus conference report on pulmonary complications of cystic fibrosis, Pediatr. Pulmonol, 15, 187, 10.1002/ppul.1950150311
Strausbaugh, 2007, Cystic fibrosis: a review of epidemiology and pathobiology, Clin. Chest Med, 28, 279, 10.1016/j.ccm.2007.02.011
Sturgess, 1982, Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants, Am. J. Pathol, 106, 303
Wang, 1984, Association of respiratory viral infections with pulmonarydeterioration in patients with cystic fibrosis, N. Engl. J. Med., 311, 1653, 10.1056/NEJM198412273112602
