Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosis-Reference-Cited by-同舟云学术

Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosis

Published:2020-04-13 Issue:6 Volume:10 Page:748-754
ISSN:2042-6976
Container-title:International Forum of Allergy & Rhinology
language:en
Short-container-title:Int Forum Allergy Rhinol.

Author:

Dalesio Nicholas M.¹²^ORCID,Aksit Melis A.³,Ahn Kwangmi⁴,Raraigh Karen S.³,Collaco Joseph M.⁵,McGrath‐Morrow Sharon⁵,Zeitlin Pamela L.⁶,An Steven S.⁷⁸,Cutting Garry R.³

Affiliation:

1. Division of Pediatric Anesthesia/Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine Johns Hopkins University Baltimore MD

2. Department of Otolaryngology/Head & Neck Surgery Johns Hopkins University Baltimore MD

3. McKusick‒Nathans Institute of the Department of Genetic Medicine Johns Hopkins University Baltimore MD

4. Genetic Epidemiology Research Branch National Institute of Mental Health Bethesda MD

5. Department of Pediatric Pulmonology Johns Hopkins University Baltimore MD

6. Department of Pediatrics National Jewish Health Denver CO

7. Department of Pharmacology, Rutgers‐Robert Wood Johnson Medical School The State University of New Jersey Piscataway NJ

8. Rutgers Institute for Translational Medicine and Science New Brunswick NJ

Funder

Cystic Fibrosis Foundation

National Science Foundation

Publisher

Wiley

Subject

Otorhinolaryngology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/alr.22548

Reference34 articles.

1. Treatment and prognosis of nasal polyps in cystic fibrosis;Stern RC;Am J Dis Child,1982

2. Upper respiratory disease, sinusitis, and polyposis;King VV;Clin Rev Allergy,1991

3. Sinonasal Quality of Life in Children With Cystic Fibrosis

4. Contemporary management of rhinosinusitis and cystic fibrosis

5. Cystic Fibrosis—An Otolaryngologic Perspective

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