hereditary condition that is passed on from parents to their children through genes. This condition may result in serious lung disease in adults and/or liver disease in infants, children and adults. Alpha-1 occurs when there is a severe lack of a protein in the blood called alpha-1 antitrypsin (AAT) that is mainly produced by the liver. The main function of AAT is to protect the lungs from inflammation caused by infection and inhaled irritants such as tobacco smoke. The low level of AAT in the blood occurs because the AAT is abnormal and cannot be released from the liver at the normal rate. This leads to a build up o
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
AAT is a protease inhibitor targeting neutrophil elastase. It prevents the destruction of tissue, pa...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Although a less well-known consequence of alpha-1 antitrypsin deficiency (AATD) liver disease is the...
Alpha-1 antitrypsin (A1AT) is the most abundant serine protease inhibitor in human blood and exerts ...
SummaryObjectiveTo review the topic of alpha-1 antitrypsin (AAT) deficiency.MethodNarrative literatu...
OBJECTIVE: To review the topic of alpha-1 antitrypsin (AAT) deficiency. METHOD: Narrative literature...
Alpha1-antitrypsin deficiency (A1ATD) is an inherited cause of chronic liver disease. It is inherite...
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Introduction: Alpha1 antitrypsin deficiency (AATD), a common hereditary disorder affecting mainly lu...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
AAT is a protease inhibitor targeting neutrophil elastase. It prevents the destruction of tissue, pa...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Although a less well-known consequence of alpha-1 antitrypsin deficiency (AATD) liver disease is the...
Alpha-1 antitrypsin (A1AT) is the most abundant serine protease inhibitor in human blood and exerts ...
SummaryObjectiveTo review the topic of alpha-1 antitrypsin (AAT) deficiency.MethodNarrative literatu...
OBJECTIVE: To review the topic of alpha-1 antitrypsin (AAT) deficiency. METHOD: Narrative literature...
Alpha1-antitrypsin deficiency (A1ATD) is an inherited cause of chronic liver disease. It is inherite...
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Introduction: Alpha1 antitrypsin deficiency (AATD), a common hereditary disorder affecting mainly lu...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
AAT is a protease inhibitor targeting neutrophil elastase. It prevents the destruction of tissue, pa...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...