Background: Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is associated with increased risk of liver disease and chronic obstructive pulmonary disease (COPD), but the risk of venous thromboembolism (VTE) is unknown. Our aim was to evaluate the risk of VTE in individuals with severe AATD compared with control subjects from the general population. Methods: Individuals with severe AATD (n = 1577) were recruited from the Swedish national AATD register. Control subjects (n = 5969) were selected from the OLIN (Obstructive Lung Disease in Northern Sweden) studies, that include a random general population sample. Longitudinal data on VTE and diagnoses were obtained from the Swedish National Patient Registry. Associations were analyz...
BACKGROUND: Previous studies of non-smoking individuals with severe alpha-1-antitrypsin deficiency (...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
Background: Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is associated with increas...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is an established risk factor for chronic o...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is an established risk factor for chronic o...
Background Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is a risk factor for pulmon...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Background Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is a risk factor for pulmon...
Background: Severe alpha 1-antitrypsin deficiency (PiZZ) predisposes to morbidity and mortality due ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
Background: The proportion of adults with liver disease due to severe alpha-1-antitrypsin deficiency...
Background: Previous studies of the natural history of alpha-1-antitrypsin (AAT) deficiency are most...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
Homozygous alpha-1-antitrypsin (AAT)deficiency (PiZZ) is known to predispose to emphysema and chroni...
BACKGROUND: Previous studies of non-smoking individuals with severe alpha-1-antitrypsin deficiency (...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...
Background: Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is associated with increas...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is an established risk factor for chronic o...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is an established risk factor for chronic o...
Background Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is a risk factor for pulmon...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Background Severe alpha-1-antitrypsin deficiency (AATD), phenotype PiZZ, is a risk factor for pulmon...
Background: Severe alpha 1-antitrypsin deficiency (PiZZ) predisposes to morbidity and mortality due ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
Background: The proportion of adults with liver disease due to severe alpha-1-antitrypsin deficiency...
Background: Previous studies of the natural history of alpha-1-antitrypsin (AAT) deficiency are most...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
Homozygous alpha-1-antitrypsin (AAT)deficiency (PiZZ) is known to predispose to emphysema and chroni...
BACKGROUND: Previous studies of non-smoking individuals with severe alpha-1-antitrypsin deficiency (...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an autosomal co-dominant condition that predisposes t...