Results 191 to 200 of about 15,020 (214)
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Variants of SERPINA1 and the increasing complexity of testing for alpha-1 antitrypsin deficiency
Therapeutic Advances in Chronic Disease, 2021Kimberly Foil
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Galactosemia and Alpha-1- antitrypsin Deficiency
Clinical Pediatrics, 1985F, Taylor +4 more
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Testing Patterns and Disparities for Alpha-1 Antitrypsin Deficiency
American Journal of Medicine, 2023Leonard Riley +2 more
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Alpha-1-antitrypsin deficiency
2009Alpha 1 antitrypsin deficiency is a rare hereditary disease with gene mutation located on 14q31-32 chromosome. Alpha 1 antitrypsin is a glycoprotein mainly produced by synthesize in the liver. It inhibits proteolytic activity in serum and thus prevents tissue damage.
Peroš-Golubičić, Tatjana +3 more
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<p>Monocytes and Macrophages in Alpha-1 Antitrypsin Deficiency</p>
International Journal of COPD, 2020Kylie B R Belchamber +2 more
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Alpha 1-antitrypsin deficiency.
Gastroenterology nursing : the official journal of the Society of Gastroenterology Nurses and Associates, 1992alpha 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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Liver disease with unknown etiology – have you ruled out alpha-1 antitrypsin deficiency?
Therapeutic Advances in Chronic Disease, 2021Dhiren Patel, Jeffrey H Teckman
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The spectrum of clinical sequelae associated with alpha-1 antitrypsin deficiency
Therapeutic Advances in Chronic Disease, 2021Vickram Tejwani, James K Stoller
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