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Publications by Michael B Robinson

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

Pediatric Research

English

Gene Therapy in the Ornithine Transcarbamylase Deficient Mouse Prevents Clinical Sequelae of Nitrogen Challenge. ▴ 886

Pediatric Research

English

Related publications

Family Studies in Ornithine Transcarbamylase Deficiency.

Archives of Disease in Childhood

English

Orthotopic Liver Transplantation for Ornithine Transcarbamylase Deficiency With Hyperammonemic Encephalopathy

Journal of Pediatric Surgery

English

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

English

803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)

Pediatric Research

English

Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis

English

Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia

Pediatric Research

English

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

Nuclear Medicine

English

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

Russkii Zhunal Detskoi Nevrologii

English

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

Pediatric Research

English