Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

End-stage liver disease in a 31-year-old man.

Seminars in liver disease - 1 Aug 1992

Sherman K E, Goodman Z D

Abstract excerpt

This is a case of decompensated chronic liver disease associated with FZ phenotype AAT deficiency. Histologic confirmation of the diagnosis was aided by immunostaining of the AAT globules. Liver transplantation was successful in reversing the disease process.

Topics

Adult
Diagnosis, Differential
Humans
Liver Cirrhosis
Liver Failure
Lung Diseases
Male
Phenotype
alpha 1-Antitrypsin
alpha 1-Antitrypsin Deficiency

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1439885
DOI: 10.1055/s-2008-1040403

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1439885-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

End-stage liver disease in a 31-year-old man.PMID 1439885Read ↗

Identification of PiZ gene products in liver tissue by a monoclonal antibody specific for the Z mutant of alpha 1-antitrypsin.Semantic proximity Read ↗

Heterozygous alpha 1-antitrypsin phenotypes in patients with end stage liver disease.Semantic proximity Read ↗

Severe alpha1-antitrypsin deficiency (PiZ homozygosity) with membranoproliferative glomerulonephritis and nephrotic syndrome, reversible after orthotopic liver transplantation.Semantic proximity Read ↗

Hepatocellular ubiquitin expression in alpha1-antitrypsin deficiency.Semantic proximity Read ↗

Liver cirrhosis associated with heterozygous alpha-1-antitrypsin deficiency type Pi MS and autoimmune features.Semantic proximity Read ↗

Heterozygous MZ alpha-1-antitrypsin deficiency in adults with chronic liver disease.Semantic proximity Read ↗

Alpha-1 antitrypsin deficiency-associated liver disease: From understudied disorder to the poster child of genetic medicineSemantic proximity Read ↗

Clinical and histologic features of adults with alpha-1 antitrypsin deficiency in a non-cirrhotic cohort.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.