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| Chacko A, Moss RB. (2020) Manifestations of pulmonary aspergillosis in pediatrics. Current Opinion in Pediatrics. 32: 389-394 |
| Robinson TE, Goris ML, Moss RB, et al. (2020) Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease. Pediatric Pulmonology |
| Nichols DP, Moss RB. (2020) Early Aspergillosis in Cystic Fibrosis and Air Trapping: Guilt by Association? American Journal of Respiratory and Critical Care Medicine |
| Kim J, Farahmand M, Dunn C, et al. (2018) Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults. Scientific Reports. 8: 16233 |
| Tracy MC, Moss RB. (2018) The myriad challenges of respiratory fungal infection in cystic fibrosis. Pediatric Pulmonology |
| Forrest OA, Chopyk DM, Gernez Y, et al. (2018) Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |
| Burgener EB, Moss RB. (2018) Cystic fibrosis transmembrane conductance regulator modulators: precision medicine in cystic fibrosis. Current Opinion in Pediatrics |
| Wagener JS, Millar SJ, Mayer-Hamblett N, et al. (2017) Lung function decline is delayed but not decreased in patients with cystic fibrosis and the R117H gene mutation. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |
| Sabino R, Carolino E, Moss RB, et al. (2017) Susceptibility of Candida albicans from Cystic Fibrosis Patients. Mycopathologia |
| Sawicki G, Konstan M, McKone E, et al. (2017) P255 Rate of lung function decline in patients with cystic fibrosis (cf) having a residual function gene mutation Thorax. 72 |