RATIONALE: α1-Antitrypsin (AAT) deficiency is one of the commonest rare respiratory disorders worldwide. Diagnosis, assessment of risk for developing chronic obstructive pulmonary disease (COPD), and management of replacement therapy require the availability of precise and updated ranges for protein serum levels. OBJECTIVE: This paper aims to provide ranges of serum AAT according to the main genotype classes in the general population. METHODS: The authors correlated mean AAT serum levels with the main SERPINA1 variants (M1Ala/M1Val (rs6647), M3 (rs1303), M2/M4 (rs709932), S (rs17580) and Z (rs28929474)) in 6057 individuals enrolled in the Swiss Cohort Study on Air Pollution and Lung Diseases in Adults (SAPALDIA) cohort. RESULTS: The followi...
Alpha-1 antitrypsin deficiency (AATD) is characterised by deficiency of AAT, the primary inhibitor o...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
BACKGROUND: Individuals with severe deficiency in serum alpha(1)-antitrypsin (AAT) concentrations ar...
serum 1-antitrypsin (AAT) concentrations are at high risk for developing chronic obstructive pulmo-n...
Cristina Martinez-González,1 Ignacio Blanco,2 Isidro Diego,3 Patricia Bueno,4 Marc Miravitlles5 1Pul...
The alpha-1 antitrypsin (AAT) haplotype Pi*S, when inherited along with the Pi*Z haplotype to form a...
Alpha-1 antitrypsin deficiency (AATD) is the only readily identifiable monogenic cause of COPD. To d...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
Alpha1-antitrypsin deficiency (AATD) is a genetic disorder characterized by reduced serum levels of ...
Background: Our earlier publications have demonstrated that alpha-1 antitrypsin (AAT) deficiency is ...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Several infrequent genetic polymorphisms in the SERPINA1 gene are known to substantially reduce conc...
Journal Article;In alpha-1 antitrypsin deficiency (AATD), the Z allele is present in 98% of cases wi...
Alpha-1 antitrypsin deficiency (AATD) is characterised by deficiency of AAT, the primary inhibitor o...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
BACKGROUND: Individuals with severe deficiency in serum alpha(1)-antitrypsin (AAT) concentrations ar...
serum 1-antitrypsin (AAT) concentrations are at high risk for developing chronic obstructive pulmo-n...
Cristina Martinez-González,1 Ignacio Blanco,2 Isidro Diego,3 Patricia Bueno,4 Marc Miravitlles5 1Pul...
The alpha-1 antitrypsin (AAT) haplotype Pi*S, when inherited along with the Pi*Z haplotype to form a...
Alpha-1 antitrypsin deficiency (AATD) is the only readily identifiable monogenic cause of COPD. To d...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
Alpha1-antitrypsin deficiency (AATD) is a genetic disorder characterized by reduced serum levels of ...
Background: Our earlier publications have demonstrated that alpha-1 antitrypsin (AAT) deficiency is ...
α1-antitrypsin deficiency (AATD) is a significantly under-recognised autosomal genetic disorder with...
Several infrequent genetic polymorphisms in the SERPINA1 gene are known to substantially reduce conc...
Journal Article;In alpha-1 antitrypsin deficiency (AATD), the Z allele is present in 98% of cases wi...
Alpha-1 antitrypsin deficiency (AATD) is characterised by deficiency of AAT, the primary inhibitor o...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...