Work

Urinary metabolomics reveals unique metabolic signatures in infants with cystic fibrosis

Year: 2018

Type: article

Source: Journal of Cystic Fibrosis

DOI: 10.1016/j.jcf.2018.10.016

Authors: B.T. Kopp, E. Joseloff, D. Goetz, B. Ingram, S.L. Heltshe, D.H. Leung, B.W. Ramsey, K. McCoy, D. Borowitz

Institutions: Nationwide Children's Hospital, Cystic Fibrosis Foundation, University at Buffalo, State University of New York, Metabolon (United States), University of Washington, Seattle Children's Research Institute, Baylor College of Medicine, Texas Children's Hospital

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: bronze

Funders: Cystic Fibrosis Foundation Therapeutics, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G2650868550, G308544354, Baby Observational and Nutritional Study of Cystic Fibrosis, G3991547501, Center for Cystic Fibrosis Translational Research in the Post-CFTR modulator Era

OpenAlex ID: W2901965835

FWCI: 1.521

Cites: 36

Cited by: 14

Related to: 10