A Checoury

ASL mRNA-LNP Therapeutic for the Treatment of Argininosuccinic Aciduria Enables Survival Benefit in a Mouse Model

Teratogen update: Congenital rubella

Aicardi‐Goutières syndrome: An update and results of interferon‐α studies

Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

Citrulline as a biomarker of intestinal failure due to enterocyte mass reduction

Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy

Postabsorptive plasma citrulline concentration is a marker of absorptive enterocyte mass and intestinal failure in humans

Zika Virus and Birth Defects — Reviewing the Evidence for Causality

Arginine metabolism and nutrition in growth, health and disease

Trex1 Exonuclease Degrades ssDNA to Prevent Chronic Checkpoint Activation and Autoimmune Disease

Arginine remains an essential amino acid after liver transplantation in urea cycle enzyme deficiencies

Intestinal permeability – a new target for disease prevention and therapy

Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release

Complementation analysis of fatty acid oxidation disorders.

Adipocytes promote ovarian cancer metastasis and provide energy for rapid tumor growth

Liver Transplantation in Children with Urea Cycle Disorders: The Importance of Minimizing Waiting Time

Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.

Arginine metabolism: nitric oxide and beyond

Liver transplantation for ornithine transcarbamylase deficiency in a girl

Presence of an acid-labile alpha-interferon in sera from fetuses and children with congenital rubella

Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder