Ivacaftor improves rhinologic, psychologic, and sleep-related quality of life in G551D cystic fibrosis patients

Author:

McCormick Justin1,Cho Do-Yeon1,Lampkin Brooks2,Richman Joshua1,Hathorne Heather3,Rowe Steven M.45,Woodworth Bradford A.1

Affiliation:

1. Department of Otolaryngology-Head and Neck Surgery; University of Alabama at Birmingham; Birmingham AL

2. College of Medicine; University of South Alabama; Mobile AL

3. Department of Pediatrics; University of Alabama at Birmingham; Birmingham AL

4. Department of Medicine; University of Alabama at Birmingham; Birmingham AL

5. Gregory Fleming James Cystic Fibrosis Research Center; Birmingham AL

Funder

National Heart, Lung, and Blood Institute

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Otorhinolaryngology,Immunology and Allergy

Reference43 articles.

1. Evaluation of chronic rhinosinusitis management using the SNOT-22 in adult cystic fibrosis patients;Savastnao;Eur Rev Med Pharmacol Sci,2014

2. Cystic fibrosis: molecular biology and therapeutic implications;Collins;Science,1992

3. Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes;Ferril;Int Forum Allergy Rhinol,2014

4. Genetics of cystic fibrosis;Lommatzsch;Semin Respir Crit Care Med,2009

5. Breakthrough therapies: cystic fibrosis (CF) potentiators and correctors;Solomon;Pediatr Pulmonol,2015

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