A Belgian alpha-1-antitrypsin (AAT) deficiency registry has been established in 2003. Currently 55 patients are included. At the same time, a working group has been set up for publishing national guidelines. In 2014, several Belgian patients founded Alpha-1 Global. We hope that the integrated activities of all the stakeholders involved in AAT deficiency will permit a high quality care for all patients suffering from this disabling disease
In 1997, the World Health Organization recommended establishing an international registry of alpha(1...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
A Belgian alpha-1-antitrypsin (AAT) deficiency registry has been established in 2003. Currently 55 p...
A Belgian alpha-1-antitrypsin (AAT) deficiency registry has been established in 2003. Currently 55 p...
The Alpha One International Registry is a scientific foundation established to comply with a World H...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
alpha 1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels of ...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
Since the first American Thoracic Society statement regarding the diagnosis and management of sever...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
alpha(1)-Antitrypsin (AT) deficiency is a hereditary disorder that may lead to early-onset emphysema...
OBJECTIVE: To prepare new guidelines for the Canadian Thoracic Society (CTS) regarding severe alpha1...
In 1997, the World Health Organization recommended establishing an international registry of alpha(1...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...
A Belgian alpha-1-antitrypsin (AAT) deficiency registry has been established in 2003. Currently 55 p...
A Belgian alpha-1-antitrypsin (AAT) deficiency registry has been established in 2003. Currently 55 p...
The Alpha One International Registry is a scientific foundation established to comply with a World H...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
Alpha-1 antitrypsin (AAT) is a 52kDa glycosylated protein produced by the liver and secreted into th...
alpha 1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels of ...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1 antitrypsin deficiency (AATD) remains largely underdiagnosed despite recommendations of heal...
Since the first American Thoracic Society statement regarding the diagnosis and management of sever...
AbstractMost individuals with AAT deficiency have escaped detection by healthcare systems worldwide....
alpha(1)-Antitrypsin (AT) deficiency is a hereditary disorder that may lead to early-onset emphysema...
OBJECTIVE: To prepare new guidelines for the Canadian Thoracic Society (CTS) regarding severe alpha1...
In 1997, the World Health Organization recommended establishing an international registry of alpha(1...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Introduction: Alpha-1 antitrypsin deficiency (AATD) remains an underdiagnosed condition despite init...