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Publications by L G Svirklys

Family Studies in Ornithine Transcarbamylase Deficiency.

Archives of Disease in Childhood

English

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Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

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Ornithine Transcarbamylase Deficiency – The Real Cause of “Family Curse”. A Case Report

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Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis

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803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)

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Orthotopic Liver Transplantation for Ornithine Transcarbamylase Deficiency With Hyperammonemic Encephalopathy

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Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia

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Ornithine Transcarbamylase Deficiency With Persistent Abnormality in Cerebral Glutamate Metabolism in Adults

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Liver Peroxisome Damage During Acute Hepatic Failure in Partial Ornithine Transcarbamylase Deficiency

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Ornithine Transcarbamylase Deficiency Presenting as Encephalopathy During Adulthood Following Bariatric Surgery

Archives of Neurology

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