Discover Community Create You

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

[Congenital deficiency of alpha-1-antitrypsin. Long-term prognosis for the liver following neonatal cholestasis].

Acta gastro-enterologica Belgica - 1 Jan 2000

Nebbia G, Hadchouel M, Alagille D

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Age Factors
Share to alpha 1-Antitrypsin Deficiency
Share to Child, Preschool
Share to Cholestasis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Liver Diseases

Share to Prognosis

Source

Identifiers

PMID: 6333131

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Congenital deficiency of alpha-1-antitrypsin. Long-term prognosis for the liver following neonatal cholestasis].PMID 6333131Read ↗

[Neonatal cholestatic jaundice associated with alpha-1-antitrypsin deficiency].Semantic proximity Read ↗

[Neonatal cholestasis and deficiency of alpha-1-antitrypsin (author's transl)].Semantic proximity Read ↗

[alpha 1-antitrypsin deficiency and liver diseases].Semantic proximity Read ↗

Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominance.Semantic proximity Read ↗

[Hepatic involvement in hereditary alpha-1-antitrypsin deficiency].Semantic proximity Read ↗

Alpha-1-antitrypsin deficiency in children: clinical characteristics and diagnosis.Semantic proximity Read ↗

[Neonatal jaundice, hereditary hemolytic anemia].Semantic proximity Read ↗

Low Incidence of α-1 antitrypsin deficiency among babies with prolonged jaundice.Semantic proximity Read ↗

A Rare Phenotype of Alpha-1-Antitrypsin Deficiency Owing to PI*IS in a Newborn With Liver Disease.Semantic proximity Read ↗

[Cirrhosis in children and SZ phenotype alpha1-antitrypsin deficiency].Semantic proximity Read ↗

[Metabolic disorders of alpha 1-antitrypsin in primary liver cancer].Semantic proximity Read ↗

[Hereditary alpha 1-antitrypsin deficiency in children].Semantic proximity Read ↗

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