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Publications by David L Valle

803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)

Pediatric Research

English

Related publications

Family Studies in Ornithine Transcarbamylase Deficiency.

Archives of Disease in Childhood

English

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

English

Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis

English

Orthotopic Liver Transplantation for Ornithine Transcarbamylase Deficiency With Hyperammonemic Encephalopathy

Journal of Pediatric Surgery

English

Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia

Pediatric Research

English

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

Russkii Zhunal Detskoi Nevrologii

English

Ornithine Transcarbamylase Deficiency Presenting as Encephalopathy During Adulthood Following Bariatric Surgery

Archives of Neurology

English

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

Nuclear Medicine

English

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

Pediatric Research

English