Pubblicazioni

PUBBLICAZIONI 2021

  1. Averna M, Melotti P, Sorio C.
    Revisiting the Role of Leukocytes in Cystic Fibrosis.
    Cells 2021, 10(12) 3380.
  2. Barry PJ, Mall MA, Alvarez A, Colombo C, de Winter-de Groot KM, Fajac I, et al; VX18-445-104 Study Group.
    Triple Therapy for Cystic Fibrosis Phe508del-Gating and -Residual Function Genotypes.
    N Engl J Med. 2021 Aug 26;385(9):815-825.
  3. Bilton D, Fajac I, Pressler T, Clancy JP, Sands D, Minic P, Cipolli M, et al; CLEAR-110 Study Group.
    Long-term amikacin liposome inhalation suspension in cystic fibrosis patients with chronic P. aeruginosa infection.
    J Cyst Fibros. 2021 Nov;20(6):1010-1017.
  4. Campagna G, Amato A, Majo F, Ferrari G, Quattrucci S, Padoan R, et al; Gruppo di lavoro RIFC.
    Italian Cystic Fibrosis Registry (ICFR). Report 2017-2018.
    Epidemiol Prev. 2021 May-Jun;45(3 Suppl 1):1-37.
  5. Colombo C, Alicandro G, Daccò V, Gagliano V, Morlacchi LC, ... Cipolli M; Italian Cystic Fibrosis Society (SIFC) Study Group for COVID-19.
    SARS-CoV-2 infection in cystic fibrosis: A multicentre prospective study with a control group, Italy, February-July 2020.
    PLoS One. 2021 May 13;16(5):e0251527.
  6. Colombo C, Cipolli M, Daccò V, Medino P, Alghisi F, Ambroni M, et al.
    Clinical course and risk factors for severe COVID-19 among Italian patients with cystic fibrosis: a study within the Italian Cystic Fibrosis Society.
    Infection. 2021 Dec 7:1-9.
  7. Gaudino R, Dal Ben S, Cavarzere P, Volpi S, Piona C, Boner A, et al.
    Delayed age at menarche in chronic respiratory diseases.
    Eur J Clin Invest. 2021 May;51(5):e13461.
  8. Innocenti D, Masi E, Taccetti G, Genito M, Balestri E, Berghelli AR, Ciciretti MA, Collini F, Fanzaghi P, Fogazzi A, Leone P, Guarise R.
    Six minute walk test in Italian children with cystic fibrosis aged 6 and 11.
    Monaldi Arch Chest Dis 2021 Dec 28. doi: 10.4081/ monaldi.2021.2047. Online ahead of print.
  9. Khan AW, Kennedy A, Furutani E, Myers K, Frattini A, ... Cipolli M, et al.
    The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations.
    Mol Cytogenet. 2021 Nov 24;14(1):54.
  10. Lo Barco T, Ghobert AL, Lucca F, Galati G, Proietti J, Cantalupo G.
    Reversible tremor in an infant with vitamin E deficiency and cystic fibrosis.
    Lancet. 2021 Jul 10;398(10295):156.
  11. Lucca F, Cucchetto G, Volpi S, Cipolli M.
    Nontuberculous mycobacteria (NTM) in Cystic fibrosis (CF) patients over the last decade: real-life data from Verona CF center.
    Eur Respir J 2021 58: PA2197.
  12. Pedrazzi M, Vercellone S, Barberis E, Capraro M, De Tullio R, ... Melotti P, et al.
    Identification of new leukocyte biomarkers related to drug recovery of CFTR: clinical applications in cystic fibrosis.
    Int. J. Mol. Sci. 2021, 22(8), 3928.
  13. Piaggi S, Marchi E, Carnicelli V, Zucchi R, Griese M, Hector A, Sorio C, et al.
    Airways glutathione S-transferase omega-1 and its A140D polymorphism are associated with severity of inflammation and respiratory dysfunction in cystic fibrosis.
    J Cyst Fibros. 2021 Feb 11:S1569-1993(21)00033-3.
  14. Piona C, Volpi S, Zusi C, Mozzillo E, Tosco A, Franzese A, et al.
    Glucose Tolerance Stages in Cystic Fibrosis Are Identified by a Unique Pattern of Defects of Beta-Cell Function.
    J Clin Endocrinol Metab. 2021 Mar 25;106(4):e1793-e1802.
  15. Santambrogio M, Lazzeri M, Bonitta G, Guarise R, Simonetta E, Blasi F, Privitera E.
    Hospital staff practical skills and theoretical knowledge in inhaled aerosol therapy: a single centre cross-sectional observational study.
    Monaldi Arch Chest Dis. 2021 Jan 25;91(1).
  16. Taccetti G, Francalanci M, Pizzamiglio G, Messore B, Carnovale V, Cimino G, Cipolli M.
    Cystic Fibrosis: Recent Insights into Inhaled Antibiotic Treatment and Future Perspectives. Antibiotics (Basel).
    2021 Mar 22;10(3):338.
  17. Tezza G, Paiola G, Zoccante L, Gandolfi M, Smania N, Ciceri ML, et al.
    Gut-Brain Axis Exploration: Stabilometric Platform Performances in Children Affected by Functional Gastrointestinal Disorders.
    J Pediatr Gastroenterol Nutr. 2021 Mar 1;72(3):347-353.
  18. Treggiari D, Kleinfelder K, Bertini M, Tridello G, Fedrigo A, et al.
    Optical Measurements of Sweat for in Vivo Quantification of CFTR Function in Individual Sweat Glands.
    J Cyst Fibros. 2021 Sep;20(5):824-827.
  19. Treggiari D, Tridello G, Menin L, Borruso A, Pintani E, Iansa P, et al.
    Role of sweat ion ratios in diagnosing cystic fibrosis.
    Pediatr Pulmonol. 2021 Jul;56(7):2023-2028.
  20. Veschetti L, Sandri A, Patuzzo C, Melotti P, Malerba G, Lleò MM.
    Genomic characterization of Achromobacter species isolates from chronic and occasional lung infection in cystic fibrosis patients.
    Microb Genom. 2021 Jul;7(7):000606.
  21. Veschetti L, Sandri A, Patuzzo C, Melotti P, Malerba G, Lleò MM.
    Mobilome Analysis of Achromobacter spp. Isolates from Chronic and Occasional Lung Infection in Cystic Fibrosis Patients.
    Microorganisms. 2021 Jan 8;9(1):130.


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