Add to ORKGa1-Antitrypsin deficiency? 2: Genetic aspects of a1-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema ris
Lung cancer (LC) and chronic obstructive pulmonary lung diseases (COPDs; including emphysema and chr...
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
lpha1-antitrypsin (a1-AT) deficiency is a common genetic disorder, with homozygous genotype Z as the...
Emphysema is a chronic progressive lung disease characterised by abnormal permanent enlargement of a...
An association between a genetically determined deficiency of the serum enzyme al antitrypsin and pu...
Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which re...
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chr...
Alpha-1-antitrypsin deficiency is associated with variable development of airflow obstruction and em...
SummaryBackgroundAlpha-1 antitrypsin (AAT) deficiency is an autosomal-codominant disorder, caused by...
SUMMARY Deficiency of serum alphai anti-trypsin is inherited as an auto-somal recessive trait, with ...
SUMMARY A patient with a low serum concentration of a1-antitrypsin (0-1 g/l) but with an M-like phen...
α1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading ...
Fifty-one years ago, two scientists from the Malmö University, Carl Bertil Laurell and Sten Eriksson...
An increased risk for the development of emphysema occurs in all carriers of deficientvariantsofAlph...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Lung cancer (LC) and chronic obstructive pulmonary lung diseases (COPDs; including emphysema and chr...
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
lpha1-antitrypsin (a1-AT) deficiency is a common genetic disorder, with homozygous genotype Z as the...
Emphysema is a chronic progressive lung disease characterised by abnormal permanent enlargement of a...
An association between a genetically determined deficiency of the serum enzyme al antitrypsin and pu...
Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which re...
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chr...
Alpha-1-antitrypsin deficiency is associated with variable development of airflow obstruction and em...
SummaryBackgroundAlpha-1 antitrypsin (AAT) deficiency is an autosomal-codominant disorder, caused by...
SUMMARY Deficiency of serum alphai anti-trypsin is inherited as an auto-somal recessive trait, with ...
SUMMARY A patient with a low serum concentration of a1-antitrypsin (0-1 g/l) but with an M-like phen...
α1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading ...
Fifty-one years ago, two scientists from the Malmö University, Carl Bertil Laurell and Sten Eriksson...
An increased risk for the development of emphysema occurs in all carriers of deficientvariantsofAlph...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
Lung cancer (LC) and chronic obstructive pulmonary lung diseases (COPDs; including emphysema and chr...
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
lpha1-antitrypsin (a1-AT) deficiency is a common genetic disorder, with homozygous genotype Z as the...