Background: This descriptive study aimed to determine the serum level of alpha-1 antitrypsin (AAT) in patients with severe asthma. Materials and Methods: The serum level of AAT was determined in 43 patients with severe asthma. Pulmonary function tests were performed and data were analyzed by SPPS version 19 software. Result: The mean age of patients was 41±13.8 years (range 14 to 78 years). The AAT level was within the normal range (90–200 mg/dl) in 38 patients (88.4%) and less than normal in 2 patients (4.7%). Conclusion: No association was observed between the serum level of AAT and lung function in severe persistent asthmatic patients. The prevalence of AAT deficiency was low in patients with severe persistent asthma. These results must ...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
AbstractObjectiveTo explore the relations that exist between α1-antitrypsin deficiency (AATD) and as...
Background and Aims: Chronic obstructive pulmonary disease (COPD) is a kind of pulmonary diseases ch...
SummaryThis study was designed to determine the prevalence of asthma and atopy, in a large group of ...
Background: Although the etiology and disease mechanisms of asthma and alpha-1 antitrypsin deficienc...
SummaryBackgroundPersistent airflow limitation is common among patients with severe asthma, but its ...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
Background: The study of hematic concentrations of alpha1 antitrypsin (AAT) is currently one step in...
Abstract Background and objective Severe alpha1 antitrypsin deficiency has been clearly associated w...
Serum α(1)-Antitrypsin (α(1)-AT) and α(1)-Acid glycoprotein (α(1)-AG) levels were measured in 34 hea...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
[Background] Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults,...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
AbstractObjectiveTo explore the relations that exist between α1-antitrypsin deficiency (AATD) and as...
Background and Aims: Chronic obstructive pulmonary disease (COPD) is a kind of pulmonary diseases ch...
SummaryThis study was designed to determine the prevalence of asthma and atopy, in a large group of ...
Background: Although the etiology and disease mechanisms of asthma and alpha-1 antitrypsin deficienc...
SummaryBackgroundPersistent airflow limitation is common among patients with severe asthma, but its ...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
Background: The study of hematic concentrations of alpha1 antitrypsin (AAT) is currently one step in...
Abstract Background and objective Severe alpha1 antitrypsin deficiency has been clearly associated w...
Serum α(1)-Antitrypsin (α(1)-AT) and α(1)-Acid glycoprotein (α(1)-AG) levels were measured in 34 hea...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
[Background] Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults,...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...