Background: Although bronchiectasis has been recognised as a feature of some patients with Alpha1-Antitrypsin deficiency the prevalence and characteristics are not widely known. We wished to determine the prevalence of bronchiectasis and patient characteristics. The first cohort of patients recruited to the EARCO (European Alpha1 Research Collaboration) International Registry data base by the end of 2021 was analysed for radiological evidence of both emphysema and bronchiectasis as well as baseline demographic features. Results: Of the first 505 patients with the PiZZ genotype entered into the data base 418 (82.8%) had a reported CT scan. There were 77 (18.4%) with a normal scan and 38 (9.1%) with bronchiectasis alone. These 2 groups wer...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Bronchiectasis is a condition of increasing incidence and prevalence around the world. Many differen...
Background: Although bronchiectasis has been recognised as a feature of some patients with Alpha1-An...
Alpha-1-antitrypsin deficiency (AATd) is a hereditary disease, mainly characterized by early onset a...
Alpha-1 antitrypsin deficiency (AATD) is a cause of bronchiectasis. Guidelines for bronchiectasis fr...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Setting: It is important to identify manifestations of alpha1-antitrypsin deficiency (A1ATD) in bron...
AbstractSettingIt is important to identify manifestations of alpha1-antitrypsin deficiency (A1ATD) i...
Rationale and objectivesAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to a...
Rationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads ...
Background: Alpha-1-antitrypsin deficiency (AATD) is a rare inherited condition caused by mutations ...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Bronchiectasis is a condition of increasing incidence and prevalence around the world. Many differen...
Background: Although bronchiectasis has been recognised as a feature of some patients with Alpha1-An...
Alpha-1-antitrypsin deficiency (AATd) is a hereditary disease, mainly characterized by early onset a...
Alpha-1 antitrypsin deficiency (AATD) is a cause of bronchiectasis. Guidelines for bronchiectasis fr...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Setting: It is important to identify manifestations of alpha1-antitrypsin deficiency (A1ATD) in bron...
AbstractSettingIt is important to identify manifestations of alpha1-antitrypsin deficiency (A1ATD) i...
Rationale and objectivesAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to a...
Rationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads ...
Background: Alpha-1-antitrypsin deficiency (AATD) is a rare inherited condition caused by mutations ...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Bronchiectasis is a condition of increasing incidence and prevalence around the world. Many differen...