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2. Covid-19 in cystic fibrosis patients compared to the general population: Severity and virus-host cell interactions

4. Large Static Testing Equipment: Design and Testing of a Settlement Facility

5. A Comparative Experimental Campaign to Estimate the Normal Interface Stiffness of Dry-Joint Masonry Structures

6. ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosis

7. Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study

17. Clinical course and risk factors for severe COVID-19 among Italian patients with cystic fibrosis: a study within the Italian Cystic Fibrosis Society

18. Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype

25. Tracking dynamic evolution of low‐ and intermediate‐risk differentiated thyroid cancer: Identification of individuals at risk of recurrence.

26. Long-term evaluation of faecal calprotectin levels in a European cohort of children with cystic fibrosis.

27. Short‐term effects of positive expiratory pressure mask on ventilation inhomogeneity in children with cystic fibrosis: A randomized, sham‐controlled crossover study

28. A survey of the prevalence, management and outcome of infants with an inconclusive diagnosis following newborn bloodspot screening for cystic fibrosis (CRMS/CFSPID) in six Italian centres

29. Clinical evaluation of an evidence-based method based on food characteristics to adjust pancreatic enzyme supplements dose in cystic fibrosis

30. Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study

31. Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020

33. Clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis: An international observational study

39. SHIFTing goals in cystic fibrosis—managing extrapulmonary disease in the era of CFTR modulator therapy; Proceedings of the International Shaping Initiatives and Future Trends (SHIFT) Symposium.

42. Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis

43. ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosis

44. The Relative Contribution of Food Groups to Macronutrient Intake in Children with Cystic Fibrosis: A European Multicenter Assessment

45. Eradication of early P. aeruginosa infection in children

47. Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7

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