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Article

[Alpha 1-antitrypsin deficiency--a hereditary storage disease of the hepatic endoplasmic reticulum].

Ceskoslovenska pediatrie - 1 Oct 1993

Stejskal J, Pijácková A, Dolezel Z, Husek K

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PMID: 8269534

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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.

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

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[Alpha 1-antitrypsin deficiency--a hereditary storage disease of the hepatic endoplasmic reticulum].PMID 8269534Read ↗

Alpha1-antitrypsin deficiency: liver disease associated with retention of a mutant secretory glycoprotein in the endoplasmic reticulum.Semantic proximity Read ↗

Hepatic endoplasmic reticulum storage diseases.Semantic proximity Read ↗

Hepatic and Extrahepatic Sources and Manifestations in Endoplasmic Reticulum Storage Diseases.Semantic proximity Read ↗

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

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

Liver disease associated with alpha 1-antitrypsin deficiency.Semantic proximity Read ↗

[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 ↗

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

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