Background and study objectives: 1-Antitrypsin (AAT) deficiency is common but underrecog-nized. A 1994 mail survey showed a long delay between the onset of symptoms and the initial diagnosis of AAT deficiency. In 2003, we carried out a similar mail survey of AAT-deficient individuals to determine whether any delay in diagnosis experienced by individuals with a more recent diagnosis had become shorter. We also determined whether individuals living near medical centers with an expressed interest in AAT deficiency experienced shorter diagnostic delays than those living at a distance. Methods: Results from mail surveys of two different cohorts were compared: a 1994 survey of 304 individuals with severe AAT deficiency and a 2003 survey of 1,953 ...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...
Background: Alpha-1 antitrypsin deficiency (AATD) is one of the most prevalent inherited diseases in...
Background: 1-Antitrypsin deficiency (AATD) is usually underrecognized, with only 5 % of cases being...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
This review summarizes the current research and outlooks regarding the obstacles to diagnosing and t...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Abstract Background Antiphospholipid Syndrome (APS) is a rare autoimmune disorder with an estimated ...
SummaryBackgroundAlpha-1-antitrypsin deficiency (AATD) is significantly underdiagnosed. The early de...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...
Background: Alpha-1 antitrypsin deficiency (AATD) is one of the most prevalent inherited diseases in...
Background: 1-Antitrypsin deficiency (AATD) is usually underrecognized, with only 5 % of cases being...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
This review summarizes the current research and outlooks regarding the obstacles to diagnosing and t...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Abstract Background Antiphospholipid Syndrome (APS) is a rare autoimmune disorder with an estimated ...
SummaryBackgroundAlpha-1-antitrypsin deficiency (AATD) is significantly underdiagnosed. The early de...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
Miriam Barrecheguren,1,2 Mónica Monteagudo,3 Pere Simonet,3–5 Carl Llor,6 Esther Rodrig...
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in ad...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
Abstract: This review summarizes the current research and outlooks regarding the obstacles to diagno...