SummaryIntroductionIndividuals with severe alpha-1-antitrypsin (AAT) deficiency have a well-known risk of developing emphysema but it is not known at which age the first symptoms occur and lung function declines. The aim of this study was to examine the prevalence of smoking, respiratory symptoms and lung function at the age of 30 in AAT-deficient individuals (PiZ and PiSZ) identified by neonatal screening.Material and methodsOne hundred and seven PiZ, 45 PiSZ and 197 control subjects (PiMM) filled in a questionnaire regarding smoking habits and symptoms. Ninety PiZ, 40 PiSZ and 84 control subjects underwent spirometry including FEV1 and FVC.ResultsTwenty-one percent of PiZ, 23% of PiSZ and 34% of PiMM subjects had smoked at some time (p<0....
BACKGROUND: Severe alpha 1-antitrypsin (AAT) deficiency (PiZZ) is associated with an increased risk ...
Individuals identified in the Swedish neonatal alpha1-antitrypsin (AAT) screening study were followe...
Children with alpha 1-antitrypsin deficiency, screened at birth, were followed prospectively. At 16 ...
SummaryIntroductionIndividuals with severe alpha-1-antitrypsin (AAT) deficiency have a well-known ri...
Introduction: Individuals with severe alpha-1-antitrypsin (AAT) deficiency have a well-known risk of...
BACKGROUND: Alpha-1-antitrypsin (AAT) deficiency increases the risk of emphysema, especially in smok...
SummaryBackgroundAlpha-1-antitrypsin (AAT) deficiency increases the risk of emphysema, especially in...
Background: Severe alpha 1-antitrypsin (AAT) deficiency (genotype PiZZ) is a well-known risk factor ...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
SummaryBackgroundThe role of lung function monitoring in subjects identified as having asymptomatic ...
Background: Alpha-1-antitrypsin (AAT) deficiency is a hereditary disorder that predisposes to emphys...
Behrouz Mostafavi,1 Sandra Diaz,2 Eeva Piitulainen,1 Berend C Stoel,3 Per Wollmer,4 Hanan A Tanash1 ...
Abstract Alpha-1-antitrypsin (AAT) deficiency is a genetic risk factor for pulmonary emphysema. In 1...
Hereditary alpha1-antitrypsin (AAT) deficiency predisposes to liver disease and emphysema. The aims ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
BACKGROUND: Severe alpha 1-antitrypsin (AAT) deficiency (PiZZ) is associated with an increased risk ...
Individuals identified in the Swedish neonatal alpha1-antitrypsin (AAT) screening study were followe...
Children with alpha 1-antitrypsin deficiency, screened at birth, were followed prospectively. At 16 ...
SummaryIntroductionIndividuals with severe alpha-1-antitrypsin (AAT) deficiency have a well-known ri...
Introduction: Individuals with severe alpha-1-antitrypsin (AAT) deficiency have a well-known risk of...
BACKGROUND: Alpha-1-antitrypsin (AAT) deficiency increases the risk of emphysema, especially in smok...
SummaryBackgroundAlpha-1-antitrypsin (AAT) deficiency increases the risk of emphysema, especially in...
Background: Severe alpha 1-antitrypsin (AAT) deficiency (genotype PiZZ) is a well-known risk factor ...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
SummaryBackgroundThe role of lung function monitoring in subjects identified as having asymptomatic ...
Background: Alpha-1-antitrypsin (AAT) deficiency is a hereditary disorder that predisposes to emphys...
Behrouz Mostafavi,1 Sandra Diaz,2 Eeva Piitulainen,1 Berend C Stoel,3 Per Wollmer,4 Hanan A Tanash1 ...
Abstract Alpha-1-antitrypsin (AAT) deficiency is a genetic risk factor for pulmonary emphysema. In 1...
Hereditary alpha1-antitrypsin (AAT) deficiency predisposes to liver disease and emphysema. The aims ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
BACKGROUND: Severe alpha 1-antitrypsin (AAT) deficiency (PiZZ) is associated with an increased risk ...
Individuals identified in the Swedish neonatal alpha1-antitrypsin (AAT) screening study were followe...
Children with alpha 1-antitrypsin deficiency, screened at birth, were followed prospectively. At 16 ...