Publications

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.

Title	Author(s)
A Little CFTR Goes a Long Way: CFTR-Dependent Sweat Secretion from G551D and R117H-5T Cystic Fibrosis Subjects Taking Ivacaftor	Char, J. E., Wolfe, M. H., Cho, H., Park, I., Jeong, J. H., Frisbee, E., Dunn, C., Davies, Z., Milla, C., Moss, R. B., Thomas, E. A., Wine, J. J.
An amyloidogenic hexapeptide derived from amylin attenuates inflammation and acute lung injury in murine sepsis	Mahapatra S, Ying L, Ho PP, Kurnellas M, Rothbard J, Steinman L, Cornfield DN.
Anti-PcrV Antibody in Cystic Fibrosis: A Novel Approach Targeting Pseudomonas aeruginosa Airway Infection	Milla, C. E., Chmiel, J. F., Accurso, F. J., VanDevanter, D. R., Konstan, M. W., Yarranton, G., Geller, D. E.
Asthma, tobacco smoke and the indoor environment: a qualitative study of sheltered homeless families	Buu, M. C., Carter, L., Bruce, J. S., Baca, E. A., Greenberg, B., Chamberlain, L. J.
B1 subunit of the Calcium-sensitive K+ channel Modulates the Pulmonary Vascular Response to Hypoxia	Barnes, E.A, Barnes, S., Lee., L., Alvira, C.M., Cornfield, D.N.
Bronchiolitis: Doing less and still getting better	Cornfield, D.N.
Chest CT in Children: Anesthesia and Atelectasis	Newman, B., Krane, E. J., Holmes, T. R., Robinson, T. E.
Combining business training, microfinance and support group involvement improves economic status and decreases intimate partner violence in an unplanned settlement of Nairobi, Kenya	Sarnquist, C., Ouma, L., Lang’at, N., Lubanga, C., Sinclair, J., Baiocchi, M., Cornfield, D.N.
Complicated pneumonia: current concepts and state of the art	Tracy, M. C., Mathew, R.
Cutaneous squamous cell carcinoma in two pediatric lung transplant patients on prolonged voriconazole treatment	Wong, J. Y., Kuzel, P., Mullen, J., Lien, D., Mahmood, M., Conrad, C., Fiorillo, L.
Cystic fibrosis transmembrane conductance regulator modulators: precision medicine in cystic fibrosis	Burgener, E. B., Moss, R. B.
Differential sensitivity of outcome measures that assess progression of mild CF lung disease in school age children	Robinson, T.E., Goris, M.L., Moss, R.B., Tian, L., Kan, P., Yilma, M., McCoy, K.S., Newman, B., de Jong, P.A., Long, F.R., Brody, A.S., Behrje, R. Yates, D.P., Cornfield, D.N.
Developmental differences in focal adhesion kinase expression modulate pulmonary endothelial barrier function in response to inflammation	Ying L, Alvira CM, Cornfield DN.
Hemophagocytic lymphohistiocytosis associated with coccidiomycosis	Ramsi, M., Alvira, C.M., Cornfield, D.N.
In children with mild cystic fibrosis, specific radiologic parameters predict progression of lung disease over 2 years	Robinson, T.E., Goris, M.L., Moss, R.B., Holmes, T.H., Yilma, M., McCoy, K., Newman, B., deJong, P.A., Long, F.R., Brody, A.S., Behrje, R., Yates, D.P., Cornfield, D.N.
Interstitial lung disease in children	Kuo, C. S., Young, L. R.
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy	Shapiro, A. J., Davis, S. D., Ferkol, T., Dell, S. D., Rosenfeld, M., Olivier, K. N., Sagel, S. D., Milla, C., Zariwala, M. A., Wolf, W., Carson, J. L., Hazucha, M. J., Burns, K., Robinson, B., Knowles, M. R., Leigh, M. W.
Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)	McKone, E. F., Borowitz, D., Drevinek, P., Griese, M., Konstan, M. W., Wainwright, C., Ratjen, F., Sermet-Gaudelus, I., Plant, B., Munck, A., Jiang, Y., Gilmartin, G., Davies, J. C.
Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype	Knowles, M. R., Ostrowski, L. E., Leigh, M. W., Sears, P. R., Davis, S. D., Wolf, W. E., Hazucha, M. J., Carson, J. L., Olivier, K. N., Sagel, S. D., Rosenfeld, M., Ferkol, T. W., Dell, S. D., Milla, C. E., et al
Passive Nocturnal Physiologic Monitoring Predicts Exacerbations in Asthmatic Children	Huffaker, M., Carchia, M., Harris, B., Kethman, W., Murphy, T., Sakarovitch, C., Qin, F., Cornfield, D.N.
Patching the Pipeline: Creation and Retention of the next generation of Physician-Scientists for Child Health Research	Cornfield, D.N., Lane, R., Rosenblum, N., D., Hostetter, M., Jobe, A., Albertine, K., Aschner, J., Abman, S.H.
Pediatric lung transplantation: Promise being realized	Conrad, C., Cornfield, D.N.
Pediatric Pulmonary Medicine: At the nexus of care and discovery	Cornfield DN.
Pediatric Pulmonary Medicine: Progress at the Intersections	Cornfield, D.N.
Pulmonary artery endotheiial cell barrier function is developmentally regulated	Ying, L., Alvira, C.M., Cornfield, D.N.
Pulmonary artery smooth muscle cells HIF-1 limits endothelin expression via microRNA-543	Wang, C.C., Ying, L. Barnes, Adams, E.S., Kim, F.Y., Alvira, C.M., Cornfield, D.N.
Rape prevention through empowerment of adolescent girls	Sarnquist , C., Omondi, B., Sinclair, J., Gitau, C., Paiva, L., Mulinge, M., Cornfield, D.N., Maldonado, Y
The Effect of Combining Business Training, Microfinance, and Support Group Participation on Economic Status and Intimate Partner Violence in an Unplanned Settlement of Nairobi, Kenya	Sarnquist CC, Ouma L, Lang'at N, Lubanga C, Sinclair J, Baiocchi MT, Cornfield DN.
Treatment options in severe fungal asthma and allergic bronchopulmonary aspergillosis	Moss, R. B.
Use of an electronic medical record-enhanced checklist and electronic dashboard to decrease catheter associated blood stream infections	Pageler, N., Longhurst, C.A., Wood, M., Suermondt, J., Cornfield, D.N., Sharek, P.J., Franzon, D.

Title	Author(s)
Are Cystic Fibrosis Aspergillus fumigatus Isolates Different? Intermicrobial Interactions with Pseudomonas	Nazik, H., Moss, R. B., Karna, V., Clemons, K. V., Banaei, N., Cohen, K., Choudhary, V., Stevens, D. A.
Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): a phase 3, extension study	Konstan, M. W., McKone, E. F., Moss, R. B., Marigowda, G., Tian, S., Waltz, D., Huang, X., Lubarsky, B., Rubin, J., Millar, S. J., Pasta, D. J., Mayer-Hamblett, N., Goss, C. H., Morgan, W., Sawicki, G. S.
Autonomous sweat extraction and analysis applied to cystic fibrosis and glucose monitoring using a fully integrated wearable platform	Emaminejad, S., Gao, W., Wu, E., Davies, Z. A., Nyein, H. Y., Challa, S., Ryan, S. P., Fahad, H. M., Chen, K., Shahpar, Z., Talebi, S., Milla, C., Javey, A., Davis, R. W.
Bronchoscopy in children with tetralogy of fallot, pulmonary atresia, and major aortopulmonary collaterals	Sidell, D. R., Koth, A. M., Bauser-Heaton, H., McElhinney, D. B., Wise-Faberowski, L., Tracy, M. C., Hanley, F. L., Asija, R.
Children with Bronchiolitis on High Flow Nasal; To Feed or Not To Feed, That’s Not the Only Question	Tracy, M.C., Cornfield, D.N.
Corrections to an ATS Workshop Report on Multiple-Breath Washout Testing for Patients with Cystic Fibrosis	Subbarao, P., Milla, C. E., Morgan, W. J., Ratjen, F.
Hypoxia-inducible factor1 expression and activity is decreased in pulmonary artery smooth muscle cells in patients with pulmonary hypertension	Barnes, E.A., Chin, C-C, Sedan, O., L., Cornfield, D.N.
Lumacaftor/Ivacaftor in Patients Aged 6-11 Years with Cystic Fibrosis and Homozygous for F508del-CFTR	Milla, C. E., Ratjen, F., Marigowda, G., Liu, F., Waltz, D., Rosenfeld, M.
Lung function decline is delayed but not decreased in patients with cystic fibrosis and the R117H gene mutation	Wagener, J. S., Millar, S. J., Mayer-Hamblett, N., Sawicki, G. S., McKone, E. F., Goss, C. H., Konstan, M. W., Morgan, W. J., Pasta, D. J., Moss, R. B.
Pediatric pulmonary medicine, Then and next	Cornfield, D.N.
Respiratory complications, management and treatments for neuromuscular disease in children	Buu, M. C.
Small Colony Variants of Pseudomonas aeruginosa Display Heterogeneity in Inhibiting Aspergillus fumigatus Biofilm	Anand, R., Moss, R. B., Sass, G., Banaei, N., Clemons, K. V., Martinez, M., Stevens, D. A.
Susceptibility of Candida albicans from Cystic Fibrosis Patients	Sabino, R., Carolino, E., Moss, R. B., Banaei, N., Verissimo, C., Stevens, D. A.
The evolution of disease: chronic lung disease of infancy and pulmonary hypertension	Tracy, M.C., Cornfield, D.N.
The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements	Char, J. E., Dunn, C., Davies, Z., Milla, C., Moss, R. B., Wine, J. J.

Title	Author(s)
Allergic Bronchopulmonary Aspergillosis	Tracy, M. C., Okorie, C. A., Foley, E. A., Moss, R. B.
Are Cystic Fibrosis Aspergillus fumigatus Isolates Different? Intermicrobial Interactions with Pseudomonas	Nazik, H., Moss, R. B., Karna, V., Clemons, K. V., Banaei, N., Cohen, K., Choudhary, V., Stevens, D. A.
Assessing Differences in Mortality Rates and Risk Factors Between Hispanic and Non-Hispanic Patients With Cystic Fibrosis in California	Buu, M. C., Sanders, L. M., Mayo, J. A., Milla, C. E., Wise, P. H.
Basophil activation test determination of CD63 combined with CD203c is not superior to CD203c alone in identifying allergic bronchopulmonary aspergillosis in cystic fibrosis	Gernez, Y., Waters, J., Tirouvanziam, R., Herzenberg, L., Moss, R.
Blood basophil activation is a reliable biomarker of allergic bronchopulmonary aspergillosis in cystic fibrosis	Gernez, Y., Walters, J., Mirkovic, B., Lavelle, G. M., Colleen, D. E., Davies, Z. A., Everson, C., Tirouvanziam, R., Silver, E., Wallenstein, S., Chotirmall, S. H., McElvaney, N. G., Herzenberg, L. A., Moss, R. B.
Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents	Leigh, M. W., Ferkol, T. W., Davis, S. D., Lee, H., Rosenfeld, M., Dell, S. D., Sagel, S. D., Milla, C., Olivier, K. N., Sullivan, K. M., Zariwala, M. A., Pittman, J. E., Shapiro, A. J., Carson, J. L., Krischer, J., Hazucha, M. J., Knowles, M. R.
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review	Shapiro, A. J., Zariwala, M. A., Ferkol, T., Davis, S. D., Sagel, S. D., Dell, S. D., Rosenfeld, M., Olivier, K. N., Milla, C., Daniel, S. J., Kimple, A. J., Manion, M., Knowles, M. R., Leigh, M. W.
Diagnostic Dilemma in the Treatment of a Fatal Case of Bloody Diarrhea	Mahaptra, S. Michie, S., Sylvester, K. Cornfield, D.N.
Earth Mover's Distance (EMD): A True Metric for Comparing Biomarker Expression Levels in Cell Populations	Orlova, D. Y., Zimmerman, N., Meehan, S., Meehan, C., Waters, J., Ghosn, E. E., Filatenkov, A., Kolyagin, G. A., Gernez, Y., Tsuda, S., Moore, W., Moss, R. B., Herzenberg, L. A., Walther, G.
Effect of Media Modified To Mimic Cystic Fibrosis Sputum on the Susceptibility of Aspergillus fumigatus, and the Frequency of Resistance at One Center	Stevens, D. A., Moss, R. B., Hernandez, C., Clemons, K. V., Martinez, M.
Evaporimeter and Bubble-Imaging Measures of Sweat Gland Secretion Rates	Kim, J., Farahmand, M., Dunn, C., Davies, Z., Frisbee, E., Milla, C., Wine, J. J.
Hypoxia enhances phosphate-induced vascular smooth muscle cell calcification	Mokas, S., Larivière, R. Cornfield, D.N., Agharazi, M., Richard, D.E
Invited commentary on Curley MA, et al. Protocolized Sedation vs Usual Care in Pediatric Patients Mechanically Ventilated for Acute Respiratory Failure: A Randomized Clinical Trial	Cornfield, D.N.
In hemolytic uremic syndrome more fluid is better: a focused clinical trial shifts the paradigm	Cornfield, D.N.
Lumacaftor/Ivacaftor in Patients Aged 6-11 Years With Cystic Fibrosis Homozygous for F508del-CFTR	Milla, C. E., Ratjen, F., Marigowda, G., Liu, F., Waltz, D., Rosenfeld, M.
Pulmonary hypertension in the premature infant: a challenging comorbidity in a vulnerable popula	O’Connor, M.G. Cornfield, D.N., Austin, E.
RASA1 somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome	Macmurdo, C. F., Wooderchak-Donahue, W., Bayrak-Toydemir, P., Le, J., Wallenstein, M. B., Milla, C., Teng, J. M., Bernstein, J. A., Stevenson, D. A.
Respiratory System Involvement in Costello Syndrome	Gomez-Ospina, N., Kuo, C., Ananth, A. L., Myers, A., Brennan, M., Stevenson, D. A., Bernstein, J. A., Hudgins, L.
Sweat chloride testing: controversies and issues	Kharrazi, M., Milla, C., Wine, J.
The basophil surface marker CD203c identifies Aspergillus species sensitization in patients with cystic fibrosis	Mirkovic, B., Lavelle, G. M., Azim, A. A., Helma, K., Gargoum, F. S., Molloy, K., Gernez, Y., Dunne, K., Renwick, J., Murphy, P., Moss, R. B., Greene, C. M., Gunaratnam, C., Chotirmall, S. H., McElvaney, N. G.
The evolving spectrum of ciliopathies and respiratory disease	Milla, C. E.
There is no ‘I’ in team: New challenges for Career Development in the Era of Team Science	Libby, A., Cornfield, D.N., Abman, S.H.
Treating allergic bronchopulmonary aspergillosis: the way forward	Moss, R. B.
Unique aspects of the Developing Lung Circulation: circulation: structural development and regulation of vasomotor tone	Gao, Y., Cornfield, D.N., Thebaud, B., Stenmark, K.R., Abman, S.H., Raj, J.U.
With Thin Phenotyping and Deep Genotyping, Knowledge is Power	Cornfield, D.N.

Title	Author(s)
Cellular mechanisms of alveolar pathology in childhood interstitial lung diseases: current insights from mouse genetics	Kuo, C. S., Desai, T. J.
Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype	Davis, S. D., Ferkol, T. W., Rosenfeld, M., Lee, H., Dell, S. D., Sagel, S. D., Milla, C., Zariwala, M. A., Pittman, J. E., Shapiro, A. J., Carson, J. L., Krischer, J. P., Hazucha, M. J., Cooper, M. L., Knowles, M. R., Leigh, M. W.
Complementary and alternative medicine in pulmonology	Mark, J. D., Chung, Y.
Current State of Pediatric Lung Transplantation	Hayes, D., Benden, C., Sweet, S. C., Conrad, C. K.
Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial	Moss, R. B., Flume, P. A., Elborn, J. S., Cooke, J., Rowe, S. M., McColley, S. A., Rubenstein, R. C., Higgins, M.
Formation of a Neurosensory Organ by Epithelial Cell Slithering	Kuo, C. S., Krasnow, M. A.
Fungi in Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis	Moss, R. B.
Influence of radiation dose and reconstruction algorithm in MDCT assessment of airway wall thickness: A phantom study	Gomez-Cardona, D., Nagle, S. K., Li, K., Robinson, T. E., Chen, G.
Inhaled B2 agonist therapy increases functional residual capacity in mechanically ventilated children with respiratory failure	Ramsi, M.A., Henry, M., Milla, C.E., Cornfield, D.N.
Inhibition of Aspergillus fumigatus and Its Biofilm by Pseudomonas aeruginosa Is Dependent on the Source, Phenotype and Growth Conditions of the Bacterium	Ferreira, J. A., Penner, J. C., Moss, R. B., Haagensen, J. A., Clemons, K. V., Spormann, A. M., Nazik, H., Cohen, K., Banaei, N., Carolino, E., Stevens, D. A.
Long-term treatment with oral N-acetylcysteine: Affects lung. function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial	Conrad, C., Lymp, J., Thompson, V., Dunn, C., DAVIES, Z., CHATFIELD, B., Nichols, D., Clancy, J., Vender, R., Egan, M. E., Quittell, L., Michelson, P., Antony, V., Spahr, J., Rubenstein, R. C., Moss, R. B., Herzenberg, L. A., Goss, C. H., Tirouvanziam, R.
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR	Wainwright, C. E., Elborn, J. S., Ramsey, B. W., Marigowda, G., Huang, X., Cipolli, M., Colombo, C., Davies, J. C., De Boeck, K., Flume, P. A., Konstan, M. W., McColley, S. A., McCoy, K., McKone, E. F., Munck, A., Ratjen, F., Rowe, S. M., Waltz, D., Boyle, M. P.
Lung matrix and vascular remodeling in mechanically ventilated elastin haploinsufficient newborn mice	Hilgendorff, A., Parai, K., Ertsey, R., Navarro, E., Jain, N., Carandang, F., Peterson, J., Mokres, L., Milla, C., Preuss, S., Alcazar, M. A., Khan, S., Masumi, J., Ferreira-Tojais, N., Mujahid, S., Starcher, B., Rabinovitch, M., Bland, R.
Molecular epidemiology of Aspergillus collected from cystic fibrosis patients	Sabino, R., Ferreira, J. A., Moss, R. B., Valente, J., Verissimo, C., Carolino, E., Clemons, K. V., Everson, C., Banaei, N., Penner, J., Stevens, D. A.
Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report	Subbarao, P., Milla, C., Aurora, P., Davies, J. C., Davis, S. D., Hall, G. L., Heltshe, S., Latzin, P., Lindblad, A., Pittman, J. E., Robinson, P. D., Rosenfeld, M., Singer, F., Starner, T. D., Ratjen, F., Morgan, W.
Non-invasive monitoring of infection and rejection after lung transplantation	De Vlaminck, Martin, L., Kertesz, M., Patel, K., Kowarsky, M., Strehl, C., Cohen, G., I., Luikart, H., Neff, N., Okamoto, J., Nicolls, M.R., Cornfield, D.N., Weill, Valentine, H.A., Khush, K.K., Quake, S.R.
Pediatric Integrative Medicine in Residency (PIMR): Description of a New Online Educational Curriculum	McClafferty, H., Dodds, H., Mark, J., et al
Pediatric Pulmonary Hypertension: Guidelines from the American Heart Association and American Thoracic Society	Abman S.H., Hansmann G., Archer S.L., Ivy D.D., Adatia I., Chung W.K. Hanna B.D., Rosenzweig E.B., Raj J.U., Cornfield D.,et al
Progress in pediatric pulmonary medicine: incremental and exponential	Cornfield, D.N.
Pulmonary artery smooth muscle cell endothelin-1 modulates the pulmonary vascular response to hypoxia	Kim, F.Y., Barnes, E.A., Lee, L., Chin, C., Alvira, C.M., and Cornfield, D.N.
Pulmonary nocardiosis in an immunocompetent patient with cystic fibrosis	Schoen, L., Santoro, J. D., Milla, C., Bhargava, S.
Recent advances in cystic fibrosis	Milla, C. E., Moss, R. B.
Sleep medicine: Pediatric polysomnography revisited	Cornfield, D.N., Bhargava, S.
The basophil surface marker CD203c identifies Aspergillus species sensitization in patients with cystic fibrosis	Mirković, B., Lavelle, G. M., Azim, A. A., Helma, K., Gargoum, F. S., Molloy, K., Gernez, Y., Dunne, K., Renwick, J., Murphy, P., Moss, R. B., Greene, C. M., Gunaratnam, C., Chotirmall, S. H., McElvaney, N. G.
The pediatric microbiome and the lung	Tracy, M., Cogen, J., Hoffman, L. R.
The transient receptor potential vanilloid 4 channel modulates uterine tone during pregnancy	Ying, L., Becard, M., Iosef, C., Shortliffe, L. Han, X., Lyell, D. Alvira, C.M., Cornfield, D.N.

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