Alpha-1-antitrypsin deficiency (AATD) is an under-diagnosed condition in patients with chronic obstructive pulmonary disease (COPD). The aim of this study was to screen for AATD in Kazakh patients with COPD using dried blood spot specimens
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
OBJECTIVE: Alpha1-antitrypsin (AAT) deficiency is a recognized susceptible factor for chronic obstru...
Alpha-1-antitrypsin deficiency (AATD) is an under-diagnosed condition in patients with chronic obstr...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Background: Alphal-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chr...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
Background and Aims: Chronic obstructive pulmonary disease (COPD) is a kind of pulmonary diseases ch...
ABSTRACT: a1-Antitrypsin (a1-AT) deficiency is an underdiagnosed condition in patients with chronic ...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Setting: About 1–3% of patients with diagnosed chronic obstructive pulmonary disease (COPD) is predi...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
OBJECTIVE: Alpha1-antitrypsin (AAT) deficiency is a recognized susceptible factor for chronic obstru...
Alpha-1-antitrypsin deficiency (AATD) is an under-diagnosed condition in patients with chronic obstr...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Background: Alphal-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chr...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
Background and Aims: Chronic obstructive pulmonary disease (COPD) is a kind of pulmonary diseases ch...
ABSTRACT: a1-Antitrypsin (a1-AT) deficiency is an underdiagnosed condition in patients with chronic ...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Setting: About 1–3% of patients with diagnosed chronic obstructive pulmonary disease (COPD) is predi...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
OBJECTIVE: Alpha1-antitrypsin (AAT) deficiency is a recognized susceptible factor for chronic obstru...