Oral Health-related quality of life in pediatric patients with cystic fibrosis

Author:

Patrick Jonathan R. D.1,da Fonseca Marcio A.2,Kaste Linda M.3,Fadavi Shahrbanoo4,Shah Neal5,Sroussi Hervé6

Affiliation:

1. Pediatric Dentistry private practice; Houston Texas

2. Associate Professor and Head; Department of Pediatric Dentistry; College of Dentistry; University of Illinois at Chicago; Chicago Illinois

3. Associate Professor; Department of Pediatric Dentistry; College of Dentistry; University of Illinois at Chicago; Chicago Illinois

4. Professor, Department of Pediatric Dentistry, College of Dentistry; University of Illinois at Chicago; Chicago Illinois

5. Medical Student; St. Louis University School of Medicine; St. Louis Missouri

6. Associate Professor, Department of Oral Medicine and Diagnostic Sciences; College of Dentistry; University of Illinois at Chicago; Chicago Illinois

Funder

Ann & Robert H. Lurie Children's Hospital Clinical Research in Pulmonary Medicine, Chicago, IL

Publisher

Wiley

Subject

General Dentistry

Reference33 articles.

1. Cystic ­fibrosis;Rowe;N Engl J Med,2005

2. Cystic Fibrosis Foundation http://www.cff.org/ 2015

3. Clinical review of cystic fibrosis;Davies;BMJ,2007

4. Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines;LeGrys;J Pediatr,2007

5. Mucin-pseudomonas aeruginosa interactions promote biofilm formation and antibiotic resistance;Landry;Mol Microbiol,2006

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