Alpha1-antitrypsin (AAT) deficiency, although largely under-diagnosed, is the underlying cause of approximately 1\% of COPD cases. Lack of awareness leads to long delays in diagnostic testing. Subsequently, lifestyle and treatment choices with potentially positive effects on prognosis may be postponed.Data on the testing and diagnostic practices for AAT deficiency were derived from the University of Pavia, Italy, and the University of Marburg, Germany. In addition, a survey of physicians was undertaken to explore their awareness and attitudes toward AAT deficiency.In Pavia and Marburg, 125 and 729 patients, respectively, were identified with severe AAT deficiency between July 2006 and June 2011. The median time interval between the onset of...
<div><p>Background</p><p>Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorde...
Tècniques de genotipat; Deficiència d'alfa-1 antitripsinaTécnicas de genotipado; Deficiencia de alfa...
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Background: determining physicians' awareness about alpha-1 antitrypsin (AAT) deficiency (AATD) may ...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
Despite recent improvements, alpha(1)-antitrypsin deficiency (AATD) remains a rarely diagnosed and t...
Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder that results in debilitating illnesses l...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Background: The European Respiratory Society recently published an important statement reviewing ava...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
AbstractObjectiveTo review the topic of alpha-1 antitrypsin (AAT) deficiency.MethodNarrative literat...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
<div><p>Background</p><p>Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorde...
Tècniques de genotipat; Deficiència d'alfa-1 antitripsinaTécnicas de genotipado; Deficiencia de alfa...
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...
Summary Background Alpha 1 -antitrypsin (AAT) deficiency, although largely under-diagnosed, is the u...
Background: determining physicians' awareness about alpha-1 antitrypsin (AAT) deficiency (AATD) may ...
AbstractAlpha-1-antitrypsin deficiency is a common genetic defect associated with the development of...
Despite recent improvements, alpha(1)-antitrypsin deficiency (AATD) remains a rarely diagnosed and t...
Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder that results in debilitating illnesses l...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
SummaryBackgroundAlpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients wit...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Background: The European Respiratory Society recently published an important statement reviewing ava...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
AbstractObjectiveTo review the topic of alpha-1 antitrypsin (AAT) deficiency.MethodNarrative literat...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
<div><p>Background</p><p>Alpha-1 antitrypsin deficiency (AATD) is the most common hereditary disorde...
Tècniques de genotipat; Deficiència d'alfa-1 antitripsinaTécnicas de genotipado; Deficiencia de alfa...
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...