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1. An inflammatory Signature of Glucose Impairment in Cystic Fibrosis

2. WS06.03 Efficacy and safety of elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) in people with cystic fibrosis and ELX/TEZ/IVA-responsive, non-F508del genotypes: a phase 3, randomised, placebo-controlled trial

3. EPS3.08 Evolution through chromosomal adaptation and coexistence of selected clones: how Pseudomonas aeruginosa endures in cystic fibrosis airways and affects prognosis

4. P287 Characterisation of CFTR mutations in people with cystic fibrosis and severe liver disease who are not eligible for CFTR modulators

5. P082 Is the new modulator affecting global health outcomes over time?

25. Telemonitoring for Cystic fibrosis patients of Bambino Gesù Children's Hospital during COVID-19.

29. Clinical and microbiological monitoring of Cystic Fibrosis patients, three years of follow-up via Tele-Medicine: an empirical research.

33. Enigma africano, la ricerca di una risposta!

34. Investigating symptoms: use of questionnaires in gastroenterology

35. Ultrasonography in the assessment of gastric and gallbladder motor function

36. Acoustic radiation force impulse (ARFI) imaging with Virtual Touch Tissue Quantification in liver disease associated with cystic fibrosis in children

47. DIAGNOSIS IN ATYPICAL CF: A CASE-REPORT TO LEARN

49. CORRELATION BETWEEN STATURE AND FEV1: AN ITALIAN MULTI-CENTRIC STUDY ON 620 CF PATIENTS AGED 6–18 YEARS

50. COMPARISON AMONG AUXOLOGIC INDEXES TO EVALUATE NUTRITIONAL STATUS OF PEDIATRIC CF PATIENTS AND CREATION OF CF GROWTH CHARTS: A MULTI-CENTRIC ITALIAN STUDY

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