Continuous arteriovenous hemodiafiltration in the acute treatment of hyperammonaemia due to ornithine transcarbamylase deficiency

Renal Failure

Volumn 22, Issue 6, 2000, Pages 823-836

  Chen, Chen Yin ^a   Chen, Yung Chang ^b   Fang, Ji Tseng ^b   Huang, Chiu Ching ^b  

^a CHANG GUNG CHILDREN S HOSPITAL   (Taiwan)

^b CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

Author keywords

Continuous arteriovenous hemofiltration; Hyperammonemia; Inborn errors; Ornithine transcarbamylase deficiency

Indexed keywords

AMMONIA; ORNITHINE CARBAMOYLTRANSFERASE;

AMMONIA BLOOD LEVEL; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; EXCHANGE BLOOD TRANSFUSION; HEMODIALYSIS; HUMAN; HYPERAMMONEMIA; MALE; NEWBORN; PERITONEAL DIALYSIS; PRIORITY JOURNAL; UREA CYCLE;

HEMODIAFILTRATION; HEMOFILTRATION; HUMANS; HYPERAMMONEMIA; INFANT, NEWBORN; MALE; ORNITHINE CARBAMOYLTRANSFERASE;

EID: 0033746338     PISSN: 0886022X     EISSN: None     Source Type: Journal    
DOI: 10.1081/JDI-100101968     Document Type: Article

References (23)

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8. Continuous venovenous hemofiltration in the acute treatment of inborn errors of metabolism
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17. Efficiency of hemodialysis therapy for a urea cycle defect in a neonale
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19. Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency
20. The addition of aminoacids and phosphate to hemodiafiltration solutions in newborns with hyperammonemic coma
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23. Liver transplantation for ornithine transcarbamylase deficiency in a girl