Bronchi Cystic Fibrosis

Fully Automatic Assessment of Bronchus-Artery Dimensions and Ratios, Mucus Plugs, and Low Attenuation Regions in Cystic Fibrosis Patients Before and After Elexacaftor-Tezacaftor-Ivacaftor

Leyla Suleymanova2024-05-29T11:18:43+00:00

Fully Automatic Assessment of Bronchus-Artery Dimensions and Ratios, Mucus Plugs, and Low Attenuation Regions in Cystic Fibrosis Patients Before and After Elexacaftor-Tezacaftor-IvacaftorLeyla Suleymanova2024-05-29T11:18:43+00:00

Azithromycin reduces bronchial wall thickening in infants with cystic fibrosis

Leyla Suleymanova2024-05-07T12:21:50+00:00

Azithromycin reduces bronchial wall thickening in infants with cystic fibrosisLeyla Suleymanova2024-05-07T12:21:50+00:00

The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6–11 with cystic fibrosis in a real-world setting

Leyla Suleymanova2023-10-23T11:24:52+00:00

The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6–11 with cystic fibrosis in a real-world settingLeyla Suleymanova2023-10-23T11:24:52+00:00

Automatic Bronchus and Artery Analysis on Chest Computed Tomography to Evaluate the Effect of Inhaled Hypertonic Saline in Children Aged 3-6 Years With Cystic Fibrosis in a Randomized Clinical Trial

Leyla Suleymanova2023-10-23T11:24:56+00:00

Automatic Bronchus and Artery Analysis on Chest Computed Tomography to Evaluate the Effect of Inhaled Hypertonic Saline in Children Aged 3-6 Years With Cystic Fibrosis in a Randomized Clinical TrialLeyla Suleymanova2023-10-23T11:24:56+00:00

Sensitive automated airway-artery method to monitor progression of CF airway disease

Leyla Suleymanova2023-10-23T11:24:57+00:00

Sensitive automated airway-artery method to monitor progression of CF airway diseaseLeyla Suleymanova2023-10-23T11:24:57+00:00

Objective airway artery dimensions compared to CT scoring methods assessing structural cystic fibrosis lung disease

Leyla Suleymanova2023-10-23T11:34:53+00:00

Objective airway artery dimensions compared to CT scoring methods assessing structural cystic fibrosis lung diseaseLeyla Suleymanova2023-10-23T11:34:53+00:00