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Article

Early-onset hepatic fibrosis in lysinuric protein intolerance.

Journal of pediatric gastroenterology and nutrition - 1 Dec 2011

Shinawi Marwan, Dietzen Dennis J, White Frances V, Sprietsma Laurie, Weymann Alexander

Abstract excerpt

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Share to Amino Acid Metabolism, Inborn Errors
Share to Child, Preschool
Share to Citrulline
Share to Liver

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Liver Cirrhosis

Share to Lysine

Share to Mutation

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Source

Identifiers

PMID: 21716135
DOI: 10.1097/MPG.0b013e318227b02d

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Early-onset hepatic fibrosis in lysinuric protein intolerance.PMID 21716135Read ↗

Overview of symptoms and treatment for lysinuric protein intoleranceSemantic proximity Read ↗

Lysinuric protein intolerance: mechanisms of pathophysiology.Semantic proximity Read ↗

Metabolic liver disease in the young adult.Semantic proximity Read ↗

Update on Lysinuric Protein Intolerance, a Multi-faceted Disease Retrospective cohort analysis from birth to adulthood.Semantic proximity Read ↗

Lysinuric protein intolerance: one gene, many problems.Semantic proximity Read ↗

Cirrhotic Cardiomyopathy: A New Clinical Phenotype.Semantic proximity Read ↗

Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationSemantic proximity Read ↗

Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders.Semantic proximity Read ↗

Correction of aging phenotype in the liver.Semantic proximity Read ↗

CUGC for lysinuric protein intolerance (LPI).Semantic proximity Read ↗

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