Disease | bronchiectasis |
Phenotype | C0010674|cystic fibrosis |
Sentences | 7 |
PubMedID- 24719116 | Atd should be considered in the differential diagnosis of bronchiectasis along with cystic fibrosis, primary immunodeficiency, allergic bronchopulmonary aspergillosis and disorders that affect ciliary function, such as primary ciliary dyskinesia. |
PubMedID- 20456672 | Early bronchiectasis in cystic fibrosis detected by surveillance ct. |
PubMedID- 21131649 | Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis. |
PubMedID- 22315518 | The target population had a diagnosis of copd (icd-9-cm codes 491.xx, 492.xx, 496.xx) in any field in the pre-index period or 60 days after the index date; absence of exclusionary comorbid conditions (respiratory cancer, cystic fibrosis, fibrosis due to tuberculosis, and bronchiectasis, pneumoconiosis, pulmonary fibrosis, pulmonary tuberculosis, sarcoidosis) during the 1 year pre-index or post-index (follow-up) periods; and an index date occurring during the enrollment period. |
PubMedID- 23692169 | Risk factors for bronchiectasis in children with cystic fibrosis. |
PubMedID- 22340019 | The following conditions occurring in the pre- or post-index period were reasons for exclusion: respiratory cancer, cystic fibrosis, fibrosis due to tuberculosis, bronchiectasis, pneumonoconiosis, pulmonary fibrosis, pulmonary tuberculosis. |
PubMedID- 25131052 | We report 4 cases found at this analyses: 3 in patients with cystic fibrosis and 1 in a patient with bronchiectasis due to kartagener syndrome. |
Page: 1