Title Author(s)
3D Printing and the Cystic Fibrosis Lung Mirza AA, Robinson TE, Gifford K, Guo HH.
Absence of evidence that respiratory viral infections influence pediatric lung transplantation outcomes: Results of the CTOTC-03 study Sweet SC, Chin H, Conrad C, Hayes D Jr, Heeger PS, Faro A, Goldfarb S, Melicoff-Portillo E, Mohanakumar T, Odim J, Schecter M, Storch GA, Visner G, Williams NM, Kesler K, Danziger-Isakov L.
Approaching Clinical Trials in Childhood Interstitial Lung Disease and Pediatric Pulmonary Fibrosis Deterding RR, DeBoer EM, Cidon MJ, Robinson TE, Warburton D, Deutsch GH, Young LR.
Filamentous bacteriophages are associated with chronic Pseudomonas lung infections and antibiotic resistance in cystic fibrosis Burgener EB, Sweere JM, Bach MS, Secor PR, Haddock N, Jennings LK, Marvig RL, Johansen HK, Rossi E, Cao X, Tian L, Nedelec L, Molin S, Bollyky PL, Milla CE.
Editorial: Pediatric pulmonology, ever changing, but happily in the same, old boat Cornfield DN
Influence of Inspiratory/Expiratory CT Registration on Quantitative Air Trapping Weinheimer O, Hoff BA, Fortuna AB, Fernández-Baldera A, Konietzke P, Wielpütz MO, Robinson TE, Galbán CJ.
New Algorithm for the Integration of Ultrasound Into Cystic Fibrosis Liver Disease Screening Sellers ZM, Lee LW, Barth RA, Milla C.
Pediatric Integrative Medicine in Academia: Stanford Children's Experience Ramesh G, Gerstbacher D, Arruda J, Golianu B, Mark J, Yeh AM.
Pediatric Integrative Medicine in Residency Program: Relationship between Lifestyle Behaviors and Burnout and Wellbeing Measures in First-Year Residents McClafferty H, Brooks AJ, Chen MK, Brenner M, Brown M, Esparham A, Gerstbacher D, Golianu B, Mark J, Weydert J, Yeh AM, Maizes V.
Pediatric pulmonology, ever changing, but happily in the same, old boat Cornfield DN
Pneumonia Prevention Strategies for Children With Neurologic Impairment Lin JL, Van Haren K, Rigdon J, Saynina O, Song H, Buu MC, Thakur Y, Srinivas N, Asch SM, Sanders LM.
Proof of concept for identifying cystic fibrosis from perspiration samples Zhou Z, Alvarez D, Milla C, Zare RN.
Rare Pulmonary Neuroendocrine Cells Are Stem Cells Regulated by Rb, p53, and Notch. Ouadah Y, Rojas ER, Riordan DP, Capostagno S, Kuo CS, Krasnow MA.
Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function Forrest OA, Chopyk DM, Gernez Y, Brown MR, Conrad CK, Moss RB, Tangpricha V, Peng L, Tirouvanziam R.
Salivary Thiocyanate as a Biomarker of Cystic Fibrosis Transmembrane Regulator Function Malkovskiy AV, Yacob AA, Dunn CE, Zirbes JM, Ryan SP, Bollyky PL, Rajadas J, Milla CE.
The nocturnal-polysomnogram and "non-hypoxic sleep-disordered-breathing" in children Guilleminault C, Huang YS, Chin WC, Okorie C.