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Publications by Ilana Nissim

Detecting Heterozygotes for Ornithine Transcarbamylase Deficiency: Comparison of Allopurinol Loading Test With 15NH4 Loading Study† 744

Pediatric Research

English

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Family Studies in Ornithine Transcarbamylase Deficiency.

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Orthotopic Liver Transplantation for Ornithine Transcarbamylase Deficiency With Hyperammonemic Encephalopathy

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Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

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803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)

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

Nuclear Medicine

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

Russkii Zhunal Detskoi Nevrologii

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Molecular Study of Ornithine Transcarbamylase: Otc Deficiency and Analysis of Mitochondrial Targeting of the Otc Precursor

Pediatric Research

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