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Cellular and Molecular Life Sciences : CMLS|October 7, 2016
Cystic fibrosis: a clinical viewCarlo Castellani, Baroukh M AssaelJournal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 15, 2011
Impact of the A (H1N1) pandemic influenza (season 2009-2010) on patients with cystic fibrosisLaura Viviani, Baroukh M Assael, Eitan Kerem, et al.Archives of Disease in Childhood|January 13, 2016
Sweat chloride and immunoreactive trypsinogen in infants carrying two <i>CFTR</i> mutations and not affected by cystic fibrosisCarlo Castellani, Gloria Tridello, Anna Tamanini, et al.Human Mutation|March 19, 2005
Identification of novel mutations in patients with Shwachman-Diamond syndromeElena Nicolis, Alberto Bonizzato, Baroukh M Assael, et al.European Journal of Clinical Pharmacology|March 9, 2004
Early antibiotic treatment of pseudomonas aeruginosa colonisation in cystic fibrosis: a critical review of the literatureFederico Marchetti, Luisella Giglio, Manila Candusso, et al.ERJ Open Research|April 26, 2018
Early diagnosis from newborn screening maximises survival in severe cystic fibrosisGloria Tridello, Carlo Castellani, Ilaria Meneghelli, et al.European Journal of Human Genetics : EJHG|March 3, 2005
Frequency of large CFTR gene rearrangements in Italian CF patientsCristina Bombieri, Alberto Bonizzato, Carlo Castellani, et al.Respiratory Care|September 29, 2006
Chest physiotherapy with positive airway pressure: a pilot study of short-term effects on sputum clearance in patients with cystic fibrosis and severe airway obstructionGiulia Placidi, Marta Cornacchia, Guido Polese, et al.Pediatric Pulmonology|October 1, 2015
Lung function comparison between two decades in cystic fibrosis children: A single centre studyGloria Tridello, Sonia Volpi, Baroukh M Assael, et al.BMC Medical Genetics|February 9, 2006
The GCC repeat length in the 5'UTR of MRP1 gene is polymorphic: a functional characterization of its relevance for cystic fibrosisElena Nicolis, Matteo Pasetto, Cristina Cigana, et al.Pageof 4