SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-antitrypsin deficiency (AATD). Guidelines are available to address physicians towards subjects at high risk for AATD. We wanted to investigate the clinical characteristics of subjects enrolled in the programme, who result as not being affected by severe AATD; this information is not available in the present literature. We elaborated data contained in the questionnaires accompanying the samples of 2127 Italian subjects submitted for AATD detection in a period spanning 11 years (1996–2006).A total of 588 subjects were eligible to enter this study: PI*MM subjects and subjects with intermediate AATD, referred for lung disease, were characterised ...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Background Alpha-1 antitrypsin deficiency (AATD) is an under-recognised genetic cause of chronic obs...
Rationale and objectivesAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to a...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
Targeted detection programmes are recommended to identify subjects affected by severe alpha1-antitry...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is under-recognized, probably because many indi...
SummaryScreening studies reveal a much larger number of individuals expected to have alpha-1 antitry...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Abstractα1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels ...
Rationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads ...
Abstract Objectives Alpha1-antitrypsin deficienc...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Background Alpha-1 antitrypsin deficiency (AATD) is an under-recognised genetic cause of chronic obs...
Rationale and objectivesAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to a...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
Targeted detection programmes are recommended to identify subjects affected by severe alpha1-antitry...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is under-recognized, probably because many indi...
SummaryScreening studies reveal a much larger number of individuals expected to have alpha-1 antitry...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
Abstractα1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels ...
Rationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads ...
Abstract Objectives Alpha1-antitrypsin deficienc...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Background Alpha-1 antitrypsin deficiency (AATD) is an under-recognised genetic cause of chronic obs...
Rationale and objectivesAlpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to a...