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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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Alpha-1-Antitrypsin Deficiency and Viral Infections
Vox Sanguinis, 1993A, Montanelli +3 more
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alpha-1-Antitrypsin deficiency.
Hepatology (Baltimore, Md.), 1984Liver disease related to alpha-1-antitrypsin deficiency occurs only in Pi ZZ homozygous children. Eleven per cent of Pi ZZ infants present with prolonged neonatal cholestasis. In our group, 25 of 45 Pi ZZ infants with prolonged neonatal cholestasis presented with later cirrhosis.
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The Role of Neutrophils in Alpha-1 Antitrypsin Deficiency
Annals of the American Thoracic Society, 2016Emer P Reeves, Cormac Mccarthy
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Alpha-1 Antitrypsin Deficiency: Pathogenesis, Clinical Presentation, Diagnosis, and Treatment
American Journal of Medicine, 2008Thomas Köhnlein
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Alpha-1-Antitrypsin Deficiency and Bronchiectasis: A Concomitance or a Real Association?
International Journal of Environmental Research and Public Health, 2020Marialuisa Bocchino +2 more
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The Challenge of Detecting Alpha-1 Antitrypsin Deficiency
COPD: Journal of Chronic Obstructive Pulmonary Disease, 2013James Stoller, Mark Brantly
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