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Alpha-1-antitrypsin augmentation therapy for alpha-1-antitrypsin deficiency

The American Journal of Medicine, 1988
Alpha-1-antitrypsin (A1AT) deficiency is a genetic disorder characterized by low serum levels of A1AT and a high risk for the development of emphysema. A1AT is the principal inhibitor of neutrophil elastase, such that a deficiency of A1AT results in insufficient anti-elastase protection in the lower respiratory tract, thus allowing neutrophil elastase ...
R C, Hubbard, R G, Crystal
openaire   +2 more sources

[Alpha 1-antitrypsin deficiency].

Revue des maladies respiratoires, 2016
Pulmonary emphysema and liver disease are the clinical expressions of alpha 1-antitrypsin deficiency, an autosomal recessive genetic disease.Alpha 1-antitrypsin deficiency is usually associated with the homozygous Z variant of the SERPINA1 gene.
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Detecting Alpha-1 Antitrypsin Deficiency

Annals of the American Thoracic Society, 2016
Alpha-1 antitrypsin deficiency is a widely underrecognized condition, with evidence of persisting long diagnostic delays and patients' frequent need to see multiple physicians before initial diagnosis. Reasons for underrecognition include inadequate understanding of alpha-1 antitrypsin deficiency by physicians and allied health care providers; failure ...
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Deficiency of Alpha-1 Antitrypsin

Annals of Internal Medicine, 1973
Excerpt It is almost a decade since genetic deficiency of alpha-1 antitrypsin was discovered in Malmo, Sweden, by Laurell and Eriksson (1) and shown to be associated with a tendency to early-onset ...
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Alpha-1 antitrypsin deficiency

The Nurse Practitioner, 2014
Cathy R, Kessenich, Kathryn, Bacher
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MZ Alpha-1 Antitrypsin Deficiency

American Journal of Respiratory and Critical Care Medicine, 2022
Oliver J, McElvaney   +4 more
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SARS-CoV-2 variant biology: immune escape, transmission and fitness

Nature Reviews Microbiology, 2023
Alessandro Maria Carabelli   +2 more
exaly  

Alpha 1-antitrypsin deficiency.

Gastroenterology nursing : the official journal of the Society of Gastroenterology Nurses and Associates, 1992
alpha 1-Antitrypsin (AAT) is a polymorphic protein with many variants collectively known as the Pi system. The most common alleles are the M, S and Z, which are co-dominantly inherited. Infants with PiZZ have approximately 16% of the normal AAT serum concentration.
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