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Publications by C Partington

G389(P) a Case for Early Ammonia Testing in All Encephalopathic Patients: Female Patients With X-Linked Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

English

Related publications

1145 Ammonia Metabolism of a Patient With Ornithine Transcarbamylase Deficiency Detected by 15n Tracer Method

Pediatric Research

English

Family Studies in 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

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

English

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

Russkii Zhunal Detskoi Nevrologii

English

803 Identification of Heterozygosity for Ornithine Transcarbamylase Deficiency (Otcd)

Pediatric Research

English

Hiding in Plain Sight: A Case of Ornithine Transcarbamylase Deficiency Unmasked Post-Liver Transplantation

American Journal of Transplantation

Transplantation

English

Paternal Transmission and Slow Elimination of Mutant Alleles Associated With Late-Onset Ornithine Transcarbamylase Deficiency in Male Patients

Journal of Human Genetics

English