Pseudomonasin cystic fibrosis

Pneumonectomy in cystic fibrosis

✍ M. Häusler; E. Franke; G. Wendt; H. Kentrup; H. Döhmen; G. Kusenbach 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 75 KB 👁 1 views

A 17-year-old boy and a 12-year-old girl with cystic fibrosis (forced expiratory volume in 1 sec, 36% and 14% of predicted values, respectively) developed severe right-sided lung infections with abscess formations and complete atelectases unresponsive to medical therapy. In both patients, unilateral

Cystic fibrosis in Ontario

✍ Sturgess, J. M. ;Czegledy-Nagy, E. ;Corey, M. ;Thompson, M. W. ;Opitz, John M. ; 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 608 KB

Complement in cystic fibrosis

✍ M. Götz; G. Lubec 📂 Article 📅 1978 🏛 Springer 🌐 English ⚖ 429 KB

Complement components C3, C4, and C3A were estimated in 30 patients with cystic fibrosis aged 1 to 21 years (M:F = 16:14) and were compared with results in 40 healthy, age-matched subjects. The influences of the clinical score, sputum microbiology, and the patients' sex were also investigated. In co

Cystic fibrosis related diabetes

✍ Alexander, S ;Bridges, N 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 488 KB

## Abstract Cystic fibrosis related diabetes is the most common co‐morbidity in cystic fibrosis. Insulin deficiency is the key factor in the development of cystic fibrosis related diabetes, which is associated with worse pulmonary and nutritional morbidity and increased mortality. The oral glucose

Cystic Fibrosis in Adults

✍ Ilma Aparecida Paschoal; Wander de Oliveira Villalba; Carmen Sílvia Bertuzzo; El 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 74 KB

Cystic fibrosis and CFTR

✍ R. Greger; R. Schreiber; M. Mall; A. Wissner; A. Hopf; M. Briel; M. Bleich; R. W 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 40 KB