Patients with decreased serum alpha^antitrypsin were designated as severely deficient ( 7 % to 15 % of normal) or intermediately deficient (30 % to 65 % of normal) by quantitative radial immunodiffusion. All severely deficient patients were symptomatic and had severe emphysema. Among intermediately deficient patients emphysema was clinically evident only after age 50. Younger subjects had significant loss of lung elastic recoil and hyperinflation without expiratory flow obstruction. Older patients with an intermediate deficiency had abnormalities that were radiographically and physiologically identical to those of younger severely deficient patients. Postmortem examination of the lung of two patients with severe deficiency and one patient w...
and severe (ZZ) a1-antitrypsin deficiency affects lung function in the population at large. Methods:...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
An association between a genetically determined deficiency of the serum enzyme al antitrypsin and pu...
SUMMARY Deficiency of serum alphai anti-trypsin is inherited as an auto-somal recessive trait, with ...
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chr...
a1-Antitrypsin deficiency? 2: Genetic aspects of a1-antitrypsin deficiency: phenotypes and genetic m...
Four clinical studies in subjects with alpha-1 antitrypsin deficiency were undertaken. The first exa...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
The aim of this study was to investigate a group of severe alpha 1-antitrypsin deficient subjects. O...
Hereditary alpha1-antitrypsin (AAT) deficiency predisposes to liver disease and emphysema. The aims ...
Abstract: Background: A congenital cause of emphysema resulting from alpha I-antitrypsin (AlAT) defi...
Alpha-1-antitrypsin deficiency was first identi-fied in 1963, together with its association with the...
Patients with homozygous alpha1 antitrypsin deficiency present a unique opportunity for evaluation o...
The current hypothesis of pulmonary emphysema is based on an alteration of the protease-antiprotease...
and severe (ZZ) a1-antitrypsin deficiency affects lung function in the population at large. Methods:...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
An association between a genetically determined deficiency of the serum enzyme al antitrypsin and pu...
SUMMARY Deficiency of serum alphai anti-trypsin is inherited as an auto-somal recessive trait, with ...
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chr...
a1-Antitrypsin deficiency? 2: Genetic aspects of a1-antitrypsin deficiency: phenotypes and genetic m...
Four clinical studies in subjects with alpha-1 antitrypsin deficiency were undertaken. The first exa...
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and i...
The aim of this study was to investigate a group of severe alpha 1-antitrypsin deficient subjects. O...
Hereditary alpha1-antitrypsin (AAT) deficiency predisposes to liver disease and emphysema. The aims ...
Abstract: Background: A congenital cause of emphysema resulting from alpha I-antitrypsin (AlAT) defi...
Alpha-1-antitrypsin deficiency was first identi-fied in 1963, together with its association with the...
Patients with homozygous alpha1 antitrypsin deficiency present a unique opportunity for evaluation o...
The current hypothesis of pulmonary emphysema is based on an alteration of the protease-antiprotease...
and severe (ZZ) a1-antitrypsin deficiency affects lung function in the population at large. Methods:...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...