Upper airway microbiota development in infants with cystic fibrosis diagnosed by newborn screen
J. Kirk Harris1, Brandie D. Wagner2, Charles E. Robertson3, Mark J. Stevens1, Conor Lingard4, Drucy Borowitz5, Daniel H. Leung6, Sonya L. Heltshe7,8, Bonnie W. Ramsey7,8, Edith T. Zemanick1
1Department of Pediatrics, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, 13123 E. 16th Ave, B-395, Aurora, CO 80045, USA
2Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, USA
3Department of Infectious Diseases, University of Colorado Anschutz Medical Campus, Aurora, CO, USA
4Spartanburg Regional Healthcare Systems, Spartanburg, SC, USA
5Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY, USA
6Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA
7Cystic Fibrosis Foundation Therapeutic Development Network Coordinating Center, Seattle Children's Research Institute, Seattle, WA, USA
8Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA
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Thông tin xuất bản
Journal of Cystic Fibrosis
Tập 22
644-651
Thông tin tác giả