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Publications by Hilary Vernon
A New Mouse Model of Mild Ornithine Transcarbamylase Deficiency (Spf-J) Displays Cerebral Amino Acid Perturbations at Baseline and Upon Systemic Immune Activation
PLoS ONE
Multidisciplinary
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Family Studies in Ornithine Transcarbamylase Deficiency.
Archives of Disease in Childhood
Child Health
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Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency
Archives of Disease in Childhood
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Ornithine Transcarbamylase Deficiency With Persistent Abnormality in Cerebral Glutamate Metabolism in Adults
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Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis
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Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia
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803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)
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Ornithine Transcarbamylase Deficiency – The Real Cause of “Family Curse”. A Case Report
Russkii Zhunal Detskoi Nevrologii
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Perinatology
Acute Extrapyramidal Syndrome in Mild Ornithine Transcarbamylase Deficiency: Metabolic Stroke Involving the Caudate and Putamen Without Metabolic Decompensation
European Journal of Pediatrics
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Orthotopic Liver Transplantation for Ornithine Transcarbamylase Deficiency With Hyperammonemic Encephalopathy
Journal of Pediatric Surgery
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