Rare alpha-1-antitrypsin phenotypes and liver-test abnormalities during infancy

Acta Paediatrica, International Journal of Paediatrics

Volumn 90, Issue 4, 2001, Pages 406-408

  Pittschieler, K ^a  

^a Regional Hospital   (Italy)

Author keywords

Emphysema; Hepatic dysfunction; 1 Antitrypsin deficiency

Indexed keywords

ALANINE AMINOTRANSFERASE; ALPHA 1 ANTITRYPSIN; GAMMA GLUTAMYLTRANSFERASE;

ALLELE; ARTICLE; CLINICAL TRIAL; DISEASE PREDISPOSITION; HUMAN; INFANT; ISOELECTRIC FOCUSING; ITALY; LIVER DISEASE; LUNG EMPHYSEMA; MAJOR CLINICAL STUDY; NEWBORN SCREENING; PHENOTYPE; PRIORITY JOURNAL; SMOKING;

EID: 0035055789     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2001.tb00440.x     Document Type: Article

References (9)

1. Heterozygotes and liver involvement
2. 1-antitrypsin deficiency
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4. 1-antitrypsin typing test evaluated
5. Cirrhosis associated with alpha-1-antitrypsin deficiency: A previously unrecognized inherited disorder
6. 1-antitrypsin deficiency
7. 1-antitrypsin deficiency
8. 1-antitrypsin deficiency, emphysema, and liver disease
9. Primary prevention in a high-risk group: Smoking habits in adolescents with homozygous alpha-1-antitrypsin deficiency (ATD)