Background The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research Collaboration (EARCO) provides information about the characteristics of patients, in particular those with the PI*SZ genotype, which is frequent in Spain. Method Individuals with severe AATD defined as proteinase inhibitor (PI) genotypes PI*ZZ, PI*SZ and other rare deficient variants were included from February 1, 2020, to February 1, 2022. The analysis focused on a comparison of the characteristics of PI*ZZ and PI*SZ patients. Results 409 patients were included (53.8% men) with a mean±SD age of 53.5±15.9 years. Genotypes were PI*ZZ in 181 (44.7%), PI*SZ in 163 (40.2%), PI*SS in 29 (7.2%) and other in 32 (7.9%). 271 (67.4%)...
The alpha-1 antitrypsin (AAT) haplotype Pi*S, when inherited along with the Pi*Z haplotype to form a...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Alpha-1-antitrypsin (α1-AT) deficiency is mainly evaluated in the diagnostic process of chronic obst...
Spanish registry; Clinical characteristicsRegistre espanyol; Característiques clíniquesRegistro espa...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
With the aim of providing better clinical characterisation of patients with α1-antitrypsin deficienc...
Alpha-1 antitrypsin deficiency (AATD), mainly due to the PI*ZZ genotype in SERPINA1, is one of the m...
The percentage of α1-antitrypsin protease inhibitor ZZ (PiZZ) genotypes in patients with COPD is con...
AbstractThe aim of the present study was to review published surveys on allelic frequencies S and Z ...
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders in...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
SERPINA1, Epidemiologia genètica; Inhibidor de la proteasaSERPINA1; Epidemiología genética; Inhibido...
Cristina Martinez-González,1 Ignacio Blanco,2 Isidro Diego,3 Patricia Bueno,4 Marc Miravitlles5 1Pul...
Genetic epidemiological studies on the prevalence and numbers of individuals with α1-antitrypsin def...
The alpha-1 antitrypsin (AAT) haplotype Pi*S, when inherited along with the Pi*Z haplotype to form a...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Alpha-1-antitrypsin (α1-AT) deficiency is mainly evaluated in the diagnostic process of chronic obst...
Spanish registry; Clinical characteristicsRegistre espanyol; Característiques clíniquesRegistro espa...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
With the aim of providing better clinical characterisation of patients with α1-antitrypsin deficienc...
Alpha-1 antitrypsin deficiency (AATD), mainly due to the PI*ZZ genotype in SERPINA1, is one of the m...
The percentage of α1-antitrypsin protease inhibitor ZZ (PiZZ) genotypes in patients with COPD is con...
AbstractThe aim of the present study was to review published surveys on allelic frequencies S and Z ...
Background. AAT deficiency is not a rare disease, but one of the most common congenital disorders in...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
SERPINA1, Epidemiologia genètica; Inhibidor de la proteasaSERPINA1; Epidemiología genética; Inhibido...
Cristina Martinez-González,1 Ignacio Blanco,2 Isidro Diego,3 Patricia Bueno,4 Marc Miravitlles5 1Pul...
Genetic epidemiological studies on the prevalence and numbers of individuals with α1-antitrypsin def...
The alpha-1 antitrypsin (AAT) haplotype Pi*S, when inherited along with the Pi*Z haplotype to form a...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
Alpha-1-antitrypsin (α1-AT) deficiency is mainly evaluated in the diagnostic process of chronic obst...