MRI and Pulmonary Function Tests’ Results as Ventilation Inhomogeneity Markers in Children and Adolescents with Cystic Fibrosis

Magnetic resonance imaging (MRI) of the chest is becoming more available in the detection and monitoring of early changes in lung function and structure in patients with cystic fibrosis (CF). The aim of this study was to assess the relationship between pulmonary function tests (PFT) and perfusion de...

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Detalles Bibliográficos
Autores principales: Wojsyk-Banaszak, Irena, Więckowska, Barbara, Szczepankiewicz, Aleksandra, Stachowiak, Zuzanna, Andrzejewska, Marta, Juchnowicz, Jerzy, Kycler, Maciej, Famulska, Paulina, Osińska, Marta, Jończyk-Potoczna, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419458/
https://www.ncbi.nlm.nih.gov/pubmed/37568538
http://dx.doi.org/10.3390/jcm12155136

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419458/
https://www.ncbi.nlm.nih.gov/pubmed/37568538
http://dx.doi.org/10.3390/jcm12155136

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