Alpha-1 antitrypsin deficiency (AATD) is an important risk factor for development of chronic obstructive pulmonary disease (COPD). Patients with AATD classically develop a different pattern of lung disease from those with usual COPD, decline faster and exhibit a range of differences in pathogenesis, all of which may be relevant to phenotype and/or impact of exacerbations. There are a number of definitions of exacerbation, with the main features being worsening of symptoms over at least 2 days, which may be associated with a change in treatment. In this article we review the literature surrounding exacerbations in AATD, focussing in particular on ways in which they may differ from such events in usual COPD, and the potential impact on clinic...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
BACKGROUND Alpha-1 antitrypsin deficiency (AATD) is a rare genetic condition predisposing individ...
Purpose: Alpha-1 antitrypsin deficiency is associated with the development of chronic obstructive pu...
SummaryBackgroundThe frequency, characteristics and impact of acute exacerbations in patients with a...
ABSTRACT: This study aimed to investigate the nature and effect of exacerbations in patients with a1...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
Patients with inherited alpha-1-antitrypsin (AAT) deficiency (ZZ-AATD) and severe chronic obstructiv...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Abstract Background The European Respiratory Society recently published an important statement revie...
Patients with inherited α1-antitrypsin (AAT) deficiency (ZZ-AATD) and severe chronic obstructive pul...
Management of lung disease in patients with alpha-1 antitrypsin deficiency (AATD) includes both non-...
Management of lung disease in patients with alpha-1 antitrypsin deficiency (AATD) includes both non-...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
BACKGROUND Alpha-1 antitrypsin deficiency (AATD) is a rare genetic condition predisposing individ...
Purpose: Alpha-1 antitrypsin deficiency is associated with the development of chronic obstructive pu...
SummaryBackgroundThe frequency, characteristics and impact of acute exacerbations in patients with a...
ABSTRACT: This study aimed to investigate the nature and effect of exacerbations in patients with a1...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
Patients with inherited alpha-1-antitrypsin (AAT) deficiency (ZZ-AATD) and severe chronic obstructiv...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Abstract Background The European Respiratory Society recently published an important statement revie...
Patients with inherited α1-antitrypsin (AAT) deficiency (ZZ-AATD) and severe chronic obstructive pul...
Management of lung disease in patients with alpha-1 antitrypsin deficiency (AATD) includes both non-...
Management of lung disease in patients with alpha-1 antitrypsin deficiency (AATD) includes both non-...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
BACKGROUND Alpha-1 antitrypsin deficiency (AATD) is a rare genetic condition predisposing individ...
Purpose: Alpha-1 antitrypsin deficiency is associated with the development of chronic obstructive pu...