Chronic obstructive pulmonary disease (COPD) is the number one disease process treated in the Pulmonary Department at the Chalmers P. Wylie VA Ambulatory Care Center (VAACC). The medical staff includes doctors, nurses, and respiratory therapists. The team works together to ensure the veteran gets the best care available. Smoking is very popular in the military, and this puts veterans at a higher risk for COPD, compared to the general public. COPD can develop at a much younger age if the patient has alpha-1 antitrypsin deficiency (AATD). Janciauskiene, Ferrotti, Laenger, Jonigk, and Luisetti (2011) point out that patients who develop COPD with certain genotypes of AATD start showing severe signs of emphysema between the ages of thirty and fi...
Cigarette smoking and poor air quality are the greatest risk factors for developing chronic obstruct...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Alpha-1 antitrypsin (AAT) deficiency is an inherited disorder that causes low levels of, or no AAT i...
AbstractSettingAbout 1–3% of patients with diagnosed chronic obstructive pulmonary disease (COPD) is...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder that results in debilitating illnesses l...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Alpha-1 antitrypsin deficiency (AATD) is a hereditary, monogenic disorder with no unique clinical fe...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
BACKGROUND Alpha-1 antitrypsin deficiency (AATD) is a rare genetic condition predisposing individ...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
The ZZ genotype of alpha-1 antitrypsin deficiency (AATD) is strongly associated with COPD, even in n...
Background: Alpha-1-antitrypsin deficiency (AATD) is a rare inherited condition caused by mutations ...
Cigarette smoking and poor air quality are the greatest risk factors for developing chronic obstruct...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Alpha-1 antitrypsin (AAT) deficiency is an inherited disorder that causes low levels of, or no AAT i...
AbstractSettingAbout 1–3% of patients with diagnosed chronic obstructive pulmonary disease (COPD) is...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder that results in debilitating illnesses l...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
Alpha-1 antitrypsin deficiency (AATD) is a hereditary, monogenic disorder with no unique clinical fe...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
BACKGROUND Alpha-1 antitrypsin deficiency (AATD) is a rare genetic condition predisposing individ...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Background: Severe alpha-1-antitrypsin deficiency (AATD) is a genetic condition predisposing to chro...
The ZZ genotype of alpha-1 antitrypsin deficiency (AATD) is strongly associated with COPD, even in n...
Background: Alpha-1-antitrypsin deficiency (AATD) is a rare inherited condition caused by mutations ...
Cigarette smoking and poor air quality are the greatest risk factors for developing chronic obstruct...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...