Errors of carbohydrate metabolism in infants and children: a survey

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Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy.

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Metabolic pathway profiling of mitochondrial respiratory chain mutants in C. elegans.

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Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency.

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Ketogenic diet, amino acid metabolism, and seizure control.

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N(epsilon)-(gamma-L-glutamyl)-L-lysine (GGEL) is increased in cerebrospinal fluid of patients with Huntington's disease.

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Child Opportunity Index: Paradoxical Risk of Pediatric Long COVID Cases.

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The effects of an integrated nutrition-sensitive WASH, gender and poultry-value chain intervention on enteropathogen carriage in Burkinabe children: A secondary outcome analysis of the SELEVER cluster-randomized trial.

The Journal of infectious diseases·2026

Gut microbiota-derived short-chain fatty acids in gallstones: mechanisms and intervention strategies.

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Errors of carbohydrate metabolism in infants and children: a survey

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Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic Acidosis.

Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy.

Metabolic pathway profiling of mitochondrial respiratory chain mutants in C. elegans.

Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency.

Ketogenic diet, amino acid metabolism, and seizure control.

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Child Opportunity Index: Paradoxical Risk of Pediatric Long COVID Cases.

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Glow-food illuminating nutritional value and enhancing taste in chronic kidney disease: a Mediterranean perspective.

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Errors of carbohydrate metabolism in infants and children: a survey

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