Results 171 to 180 of about 12,033 (186)

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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Alpha-Mannosidase-II Deficiency Results in Dyserythropoiesis and Unveils an Alternate Pathway in Oligosaccharide Biosynthesis

Cell, 1997
Hudson H Freeze, Kelley W Moremen
exaly  

Heterozygous and Homozygous Alpha1-Antitrypsin Deficiency in Patients with Pulmonary Emphysema

New England Journal of Medicine, 1969
exaly  

Hereditary Alpha1-Antitrypsin Deficiency

New England Journal of Medicine, 1968
exaly  

Heterozygous MZ Alpha1-Antitrypsin Deficiency in Adults with Chronic Active Hepatitis and Cryptogenic Cirrhosis

New England Journal of Medicine, 1981
exaly  

Alpha-1 Antitrypsin Deficiency

Gastroenterology Nursing, 2006
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Alpha1-Antitrypsin Deficiency — A Model for Conformational Diseases

New England Journal of Medicine, 2002
exaly  

Liver Transplantation for Advanced Liver Disease with Alpha-1antitrypsin Deficiency

New England Journal of Medicine, 1980
exaly  

HETEROZYGOUS ALPHA1-ANTITRYPSIN DEFICIENCY AND CIRRHOSIS IN ADULTS, A FORTUITOUS ASSOCIATION

Lancet, The, 1975
exaly  

[Alpha-1-antitrypsin deficiency].

Harefuah, 1980
G, Dinari, M, Nitzan
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