Results 181 to 190 of about 30,835,118 (203)
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The spectrum of clinical sequelae associated with alpha-1 antitrypsin deficiency

Therapeutic Advances in Chronic Disease, 2021
James K Stoller, Vickram Tejwani
exaly  

Alpha-1 Antitrypsin Deficiency

The American Journal of Medicine, 2008
openaire   +2 more sources

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.
openaire   +1 more source

COPD: Journal of Chronic Obstructive Pulmonary Disease

COPD: Journal of Chronic Obstructive Pulmonary Disease, 2020
Ronald Reilkoff
exaly  

Alpha-1-Antitrypsin Deficiency and Viral Infections

Vox Sanguinis, 1993
A, Montanelli   +3 more
openaire   +2 more sources

Clinical and histologic features of adults with alpha-1 antitrypsin deficiency in a non-cirrhotic cohort

Journal of Hepatology, 2018
Jonathan Shuster   +2 more
exaly  

alpha-1-Antitrypsin deficiency.

Hepatology (Baltimore, Md.), 1984
Liver 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.
openaire   +1 more source

The Role of Neutrophils in Alpha-1 Antitrypsin Deficiency.

Annals of the American Thoracic Society, 2016
Emer P Reeves, Cormac McCarthy
exaly  

The Challenge of Detecting Alpha-1 Antitrypsin Deficiency

COPD: Journal of Chronic Obstructive Pulmonary Disease, 2013
James K Stoller, Mark Brantly
exaly  

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