This review seeks to give an overview of alpha-1 antitrypsin deficiency, including the different disease phenotypes that it encompasses. We then describe the different therapeutic endeavors that have been undertaken to address these different phenotypes. Lastly we discuss future potential therapeutics, such as genome editing, and how they may play a role in treating alpha-1 antitrypsin deficiency
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
Alpha-1 antitrypsin (AAT) deficiency is a hereditary condition characterized by low levels of AAT in...
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads ...
sema. This article will review the clinical features of 1-anti-trypsin deficiency, the genetic mut...
Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder associated with mutations in the SERPI...
In the last 13 years, three gene therapy trials for the treatment of alpha-1 antitrypsin deficiency ...
Alpha-1 antitrypsin (A1AT) is a 52 kDa serine protease inhibitor that is synthesized in and secreted...
Introduction: Alpha1 antitrypsin deficiency (AATD), a common hereditary disorder affecting mainly lu...
INTRODUCTION: As a common monogenic disease, alpha-1 antitrypsin (AAT) deficiency has undergone thor...
Intravenous infusion of alpha-1 antitrypsin (AAT) was approved by the United States Food and Drug Ad...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1-antitrypsin deficiency (AATD) is an autosomal recessive disorder characterised by low levels...
Alpha-1 antitrypsin deficiency (AATD) is caused by mutations in the SERPINA1 gene, which encodes the...
This review summarizes the current research and outlooks regarding the obstacles to diagnosing and t...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
Alpha-1 antitrypsin (AAT) deficiency is a hereditary condition characterized by low levels of AAT in...
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads ...
sema. This article will review the clinical features of 1-anti-trypsin deficiency, the genetic mut...
Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder associated with mutations in the SERPI...
In the last 13 years, three gene therapy trials for the treatment of alpha-1 antitrypsin deficiency ...
Alpha-1 antitrypsin (A1AT) is a 52 kDa serine protease inhibitor that is synthesized in and secreted...
Introduction: Alpha1 antitrypsin deficiency (AATD), a common hereditary disorder affecting mainly lu...
INTRODUCTION: As a common monogenic disease, alpha-1 antitrypsin (AAT) deficiency has undergone thor...
Intravenous infusion of alpha-1 antitrypsin (AAT) was approved by the United States Food and Drug Ad...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decrea...
Alpha-1-antitrypsin deficiency (AATD) is an autosomal recessive disorder characterised by low levels...
Alpha-1 antitrypsin deficiency (AATD) is caused by mutations in the SERPINA1 gene, which encodes the...
This review summarizes the current research and outlooks regarding the obstacles to diagnosing and t...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
Alpha-1 antitrypsin (AAT) deficiency is a hereditary condition characterized by low levels of AAT in...
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads ...