Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results

Cystic fibrosis (CF; OMIM 219700) is a rare genetic disorder caused by a chloride channel defect, resulting in lung disease, pancreas insufficiency and liver impairment. Altered L-arginine (Arg)/nitric oxide (NO) metabolism has been observed in CF patients’ lungs and in connection with malnutrition....

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Detalles Bibliográficos
Autores principales: Brinkmann, Folke, Hanusch, Beatrice, Ballmann, Manfred, Mayorandan, Sebene, Bollenbach, Alexander, Chobanyan-Jürgens, Kristine, Jansen, Kathrin, Schmidt-Choudhury, Anjona, Derichs, Nico, Tsikas, Dimitrios, Lücke, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356307/
https://www.ncbi.nlm.nih.gov/pubmed/32604946
http://dx.doi.org/10.3390/jcm9062012

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