Background: determining physicians' awareness about alpha-1 antitrypsin (AAT) deficiency (AATD) may help to explain the discrepancy between the observed and expected number of patients diagnosed with this disease. This study was designed to assess the opinions on knowledge, practice pattern and attitude regarding AATD among physicians in Spain and Portugal. Methods: as online anonymous survey was performed on pulmonologists (n = 100), internal medicine specialists (IMS) (n = 100) and primary care physicians (PCP) (n = 176). Of the total number of physicians, 221 were from Spain, and 155 were from Portugal. Physicians answered 21 questions related to their personal and professional profile, knowledge regarding AATD and chronic obstructive pu...
BACKGROUND:Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, b...
Background: Alpha-1 antitrypsin deficiency (AATD) is one of the most prevalent inherited diseases in...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Background: determining physicians' awareness about alpha-1 antitrypsin (AAT) deficiency (AATD) may ...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Despite recent improvements, alpha(1)-antitrypsin deficiency (AATD) remains a rarely diagnosed and t...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
[Background] Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults,...
Background Augmentation therapy (AT) is the only specific treatment licensed for patients with al...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
BACKGROUND:Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, b...
Background: Alpha-1 antitrypsin deficiency (AATD) is one of the most prevalent inherited diseases in...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Background: determining physicians' awareness about alpha-1 antitrypsin (AAT) deficiency (AATD) may ...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Despite recent improvements, alpha(1)-antitrypsin deficiency (AATD) remains a rarely diagnosed and t...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
[Background] Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults,...
Background Augmentation therapy (AT) is the only specific treatment licensed for patients with al...
Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, but is under...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
BACKGROUND:Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorder in adults, b...
Background: Alpha-1 antitrypsin deficiency (AATD) is one of the most prevalent inherited diseases in...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...