19 results on '"Griese, M"'
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2. P083 Inhaled anti-pseudomonal therapy in patients with cystic fibrosis
3. 157 Long-term impact of fungi on pediatric cystic fibrosis lung disease
4. WS7.3 VX-661, an investigational CFTR corrector, in combination with ivacaftor, a CFTR potentiator, in patients with CF and homozygous for the F508Del-CFTR mutation: Interim analysis
5. WS5.1 Inhaled glutathione in cystic fibrosis
6. WS2.9 Expression and regulation of IFRD1 in neutrophils of cystic fibrosis patients
7. WS18.2 Persistent elevation of antibodies against Pseudomonas aeruginosa following successful eradication?
8. 44 Pulmonary exacerbations in a Phase 3 trial of ivacaftor in subjects with cystic fibrosis who have the G551D-CFTR mutation
9. 276* Long-term pulmonary outcome in cystic fibrosis (CF) is not adversely affected in CF associated liver disease treated with UDCA
10. 171* The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease
11. 356* Use of patient monitoring systems in clinical trials to generate objective information on patients' drug adherence of inhaled medications
12. In-vivo data support equivalent therapeutic efficacy of a new tobramycin inhalation solution (150 mg/1.5 ml) administered by the eFlow® electronic nebuliser compared to TOBI® in the PARI LC PLUS®
13. In-vitro inhibition of neutrophil elastase activity by inhaled antibiotics used in cystic fibrosis patients
14. Eradication of methicillin resistant Staphylococcus aureus in cystic fibrosis
15. e-Flow rapid®: improved lung function and patient satisfaction with more volume delivered to the lungs during inhalation therapy in cystic fibrosis
16. Reduced frequency of reactions in patients with cystic fibrosis and continuous treatment with oral cephalosporins?
17. 190 Long-term outcome after meconium ileus
18. 186 Long-term outcome of different strategies following the first isolation of Pseudomonas aeruginosa
19. 261 Continous treatment with ursodeoxycholic acid (UDCA) for 15 years
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