Work

A novel, noninvasive assay shows that distal airway oxygen tension is low in cystic fibrosis, but not in primary ciliary dyskinesia

Year: 2018

Type: article

Study design: Observational Study

Source: Pediatric Pulmonology

DOI: 10.1002/ppul.24192

Authors: Lori Mendelsohn, Christiaan Wijers, Ritika Gupta, Nadzeya Marozkina, Chun Li, Benjamin Gaston

Institutions: Rainbow Babies & Children's Hospital, Case Western Reserve University

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute

Awards: Cellular S-nitrosothiol signaling in respiratory biology, Clinical Centers for the NHLBI's Precision Interventions for Severe and/or Exacerbation Prone Asthma (PrecISE) Network (UG1), Personalized small molecule therapy for severe asthma and cystic fibrosis., Airway redox biochemistry as a deteriminant of asthma phenotype during adolescen*

OpenAlex ID: W2902953080

FWCI: 0.377

Cites: 30

Cited by: 7

Related to: 10