Liver disease in adults with α1-antitrypsin deficiency

BACKGROUND: The natural history of adult liver disease due to α1-antitrypsin deficiency (A1AD) remains poorly understood. OBJECTIVE: We investigated whether heterozygosity for the Z-allele predisposes for the development of clinically significant portal hypertension (CSPH). Moreover, we aimed to non...

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Pubblicato in:United European Gastroenterol J
Autori principali: Mandorfer, Mattias, Bucsics, Theresa, Hutya, Veronika, Schmid-Scherzer, Karin, Schaefer, Benedikt, Zoller, Heinz, Ferlitsch, Arnulf, Peck-Radosavljevic, Markus, Trauner, Michael, Ferenci, Peter, Kneussl, Meinhard, Reiberger, Thomas
Natura: Artigo
Lingua:Inglês
Pubblicazione: SAGE Publications 2018
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6068794/
https://ncbi.nlm.nih.gov/pubmed/30083333
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050640618764057
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