Alpha-1-Antitrypsin (AAT) deficiency (AATD) is a hereditary disorder that manifests primarily as pulmonary emphysema and liver cirrhosis. The clinically most relevant mutation causing AATD is a single nucleotide polymorphism Glu342Lys (Z-mutation). Despite the recommendation to test every COPD patient, the condition remains severely underdiagnosed with a delay of several years between first symptoms and diagnosis. The Grifols' AlphaKit® QuickScreen is a novel qualitative point-of-care (POC) in vitro screening test developed for the detection of the Z AAT protein in capillary whole blood. The objective of this prospective, international, multi-center, diagnostic, interventional real-world study was to assess the performance of this device fo...
Purpose/Aims: The American Thoracic Society (ATS) published recommendations for alpha-1 antitrypsin ...
Background: Alpha-1 antitrypsin (A1AT) is a protease inhibitor that protects the tissues from degrad...
Objective: Primary care provides the main route for access to health care for patients with common c...
Abstract Background Alpha-1-Antitrypsin (AAT) deficiency (AATD) is a hereditary disorder that manife...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Introduction: Alpha-1-antitrypsin deficiency (AATD), genetic risk factor for premature chronic obstr...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
Background: Alphal-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chr...
Introduction: Alpha-1-antitrypsin deficiency (AATD), genetic risk factor for premature chronic obstr...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Alpha-1 antitrypsin (A1AT or AAT) is a serine protease inhibitor (PI) which, when present at low lev...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is under-recognized, probably because many indi...
ABSTRACT: a1-Antitrypsin (a1-AT) deficiency is an underdiagnosed condition in patients with chronic ...
Purpose/Aims: The American Thoracic Society (ATS) published recommendations for alpha-1 antitrypsin ...
Background: Alpha-1 antitrypsin (A1AT) is a protease inhibitor that protects the tissues from degrad...
Objective: Primary care provides the main route for access to health care for patients with common c...
Abstract Background Alpha-1-Antitrypsin (AAT) deficiency (AATD) is a hereditary disorder that manife...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Introduction: Alpha-1-antitrypsin deficiency (AATD), genetic risk factor for premature chronic obstr...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
Background: Alphal-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chr...
Introduction: Alpha-1-antitrypsin deficiency (AATD), genetic risk factor for premature chronic obstr...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Alpha-1 antitrypsin (A1AT or AAT) is a serine protease inhibitor (PI) which, when present at low lev...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is under-recognized, probably because many indi...
ABSTRACT: a1-Antitrypsin (a1-AT) deficiency is an underdiagnosed condition in patients with chronic ...
Purpose/Aims: The American Thoracic Society (ATS) published recommendations for alpha-1 antitrypsin ...
Background: Alpha-1 antitrypsin (A1AT) is a protease inhibitor that protects the tissues from degrad...
Objective: Primary care provides the main route for access to health care for patients with common c...