HRCT in cystic fibrosis in patients with CFTR I1234V mutation: Assessment of scoring systems with low dose technique using multidetector system and correlation with pulmonary function tests

BACKGROUND AND AIMS: Pulmonary changes in patients with cystic fibrosis (CF) with CFTR I1234V mutation have not been extensively documented. Impact of geographic influence on phenotypical expression is largely unknown. This descriptive clinical study presents the high-resolution computed tomography...

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Detalles Bibliográficos
Autores principales: Bhat, Venkatraman, Wahab, Atiqa Abdul, Garg, Kailash C, Janahi, Ibrahim, Singh, Rajvir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Chest Radiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4329687/
https://www.ncbi.nlm.nih.gov/pubmed/25709165
http://dx.doi.org/10.4103/0971-3026.150144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4329687/
https://www.ncbi.nlm.nih.gov/pubmed/25709165
http://dx.doi.org/10.4103/0971-3026.150144

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