The management of life-threatening hyperammonemia: a comparison of several therapeutic modalities.

No abstract is available for this paper.

• Publication year

  1980

• Venue

  Jornal de Pediatria

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  DOI 10.1016/S0022-3476(80)80352-0PMID 7350296
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Comparison of exchange transfusion, peritoneal dialysis, and hemodialysis for the treatment of hyperammonemia in an anuric newborn infant.

  1979cited by this paper
• Two-point determination of plasma ammonia with the centrifugal analyzer.

  1978cited by this paper
• Transient hyperammonemia of the preterm infant.

  1978cited by this paper
• Peritoneal dialysis and exchange transfusion in a neonate with argininosuccinic aciduria.

  1976cited by this paper
• Long-Term Management of a Case of Carbamyl Phosphate Synthetase Deficiency Using Ketoanalogues and Hydroxyanalogues of Essential Amino Acids

  1976cited by this paper
• Long-term management of a case of carbamyl phosphate synthetase deficiency using ketanalogues and hydroxyanalogues of essential amino acids.

  1976cited by this paper
• Hemodialysis techniques for infants and children.

  1976cited by this paper
• The therapy of hyperammonemia due to ornithine transcarbamylase defiency in a male neonate.

  1975cited by this paper
• DEANOL IN SPONTANEOUS AND INDUCED DYSKINESIAS

  1975cited by this paper
• Inherited hyperammonemic syndromes.

  1974cited by this paper
• Inherited hyperammonemic syndromes.

  1974cited by this paper
• Charcoal haemoperfusion in the treatment of fulminant hepatic failure.

  1974cited by this paper
• In-Vivo Studies with a Cation Exchange Resin Mixture in the Removal of Excessive Ammonium from the Extracorporeal Circulation System.

  1971cited by this paper

• Treatment of Hyperammonemia Syndrome in Lung Transplant Recipients

  2023cites this paper
• Acute Fulminant Encephalopathy in an Adult due to Ornithine Transcarbamylase Deficiency

  2022cites this paper
• Peritoneal Dialysis in Children

  2021cites this paper
• Dialytic Therapy of Inborn Errors of Metabolism in Case of Acute Decompensation

  2021cites this paper
• Extracorporeal Ammonia Clearance for Hyperammonemia in Critically Ill Patients: A Scoping Review

  2020cites this paper
• Hyperammonemia, the Last Indication of High-Volume Hemodiafiltration in Adult and Children: A Structured Review

  2019cites this paper
• Chapter 27 – Amino Acids

  2018cites this paper
• Rapid Resolution of Hyperammonemia in Neonates Using Extracorporeal Membrane Oxygenation as a Platform to Drive Hemodialysis

  2017cites this paper
• Chapter 82 – Dialysis in Inborn Errors of Metabolism

  2017cites this paper
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• Hyperammonemia in Urea Cycle Disorders: Role of the Nephrologist

  2016cites this paper
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  2015cites this paper
• Short-term survival of hyperammonemic neonates treated with dialysis

  2015cites this paper
• Late Onset Ornithine Transcarbamylase Deficiency Accompanying Severe HyperammonemiaAfter Cesarean Section: Case Report

  2015cites this paper
• Utility of peritoneal dialysis in neonates affected by inborn errors of metabolism

  2014cites this paper
• Symptomatic hyperammonemia after lung transplantation: Lessons learnt

  2014cites this paper
• Ammonia clearance with haemofiltration in adults with liver disease

  2014influential citation
• Hyperammonemia due to urea cycle disorders: a potentially fatal condition in the intensive care setting

  2014influential citation
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  2014cites this paper
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  2012cites this paper
• Nonrenal indications for continuous renal replacement therapy: A report from the Prospective Pediatric Continuous Renal Replacement Therapy Registry Group

  2012cites this paper
• Hyperammonemia in a Patient with Late-Onset Ornithine Carbamoyltransferase Deficiency

  2012cites this paper
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  2011cites this paper
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  2011cites this paper
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  2010cites this paper
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  2009cites this paper
• Hyperammonemia from a Urea Cycle Disorder Presenting in Adulthood

  2009cites this paper
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  2009cites this paper
• Peritoneal dialysis in neonates with inborn errors of metabolism: is it really out of date?

  2008cites this paper
• Hemodialysis for hyperammonemia associated with ornithine transcarbamylase deficiency

  2008cites this paper
• CHAPTER 95 – Dialysis in Inborn Errors of Metabolism

  2008cites this paper
• Fatal initial adult-onset presentation of urea cycle defect.

  2007cites this paper
• High-Volume Continuous Venovenous Hemofiltration as an Effective Therapy for Acute Management of Inborn Errors of Metabolism in Young Children

  2007cites this paper
• Current Status of Hyperammonemic Syndromes

  2007cites this paper
• Sodium Phenylacetate and Sodium Benzoate in the Treatment of Neonatal

  2006cites this paper
• Grundsätzliche und praktische Aspekte zur Hyperammonämie im Kindesalter

  2006cites this paper
• Pharmacology Review: Sodium Phenylacetate and Sodium Benzoate in the Treatment of Neonatal Hyperammonemia

  2006cites this paper
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  2006cites this paper
• Introduction to hyperammonemia and disorders of the urea cycle

  2005cites this paper
• Comparison of solute clearance in three modes of continuous renal replacement therapy

  2004cites this paper
• [Hyperammonemia: causes, diagnosis and therapy. 2. Symptoms and therapy].

  2004cites this paper
• Hyperammonämie: Ursachen, Diagnostik, Therapie

  2004cites this paper
• Dialytic management of inborn errors of metabolism

  2004cites this paper
• Clearance of amino acids by hemodialysis in argininosuccinate synthetase deficiency.

  2004cites this paper
• Emergency dialysis in neonatal metabolic crises.

  2002cites this paper
• Ammonia detoxification by continuous venovenous haemofiltration in an infant with urea cycle defect.

  2002cites this paper
• Heliox Use in the Treatment of Acute Hyperammonemia

  2001cites this paper
• Hyperammonemia in urea cycle disorders: role of the nephrologist.

  2001cites this paper
• Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicators

  2001influential citation
• Fatal new onset metabolic encephalopathy in a 14 year old boy

  2000cites this paper
• CONTINUOUS ARTERIOVENOUS HEMODIAFILTRATION IN THE ACUTE TREATMENT OF HYPERAMMONAEMIA DUE TO ORNITHINE TRANSCARBAMYLASE DEFICIENCY

  2000cites this paper
• Dialysis in neonates with inborn errors of metabolism.

  1999cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998influential citation
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  1998cites this paper
• Indications et résultats cliniques de l'épuration extrarénale continue chez l'enfant

  1998cites this paper
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  1997cites this paper
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  1997cites this paper
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  1996cites this paper
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  1996cites this paper
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  1995cites this paper
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  1994cites this paper
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  1994cites this paper
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  1993cites this paper
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  1992cites this paper
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  1992cites this paper
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  1990cites this paper
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  1990cites this paper
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  1989cites this paper
• When and How Should We Measure Plasma Ammonia?

  1988cites this paper
• Advances in Human Genetics 15

  1986cites this paper
• The human argininosuccinate synthetase locus and citrullinemia.

  1986cites this paper
• Severe Transient Neonatal Hyperammonemia

  1986cites this paper
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  1986cites this paper
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  1985cites this paper
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  1985cites this paper
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  1985cites this paper
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  1985cites this paper
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  1985cites this paper
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  1984cites this paper
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  1983cites this paper
• Disposition of sodium benzoate in newborn infants with hyperammonemia.

  1983cites this paper
• A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disorders.

  1982cites this paper
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  1981cites this paper
• The treatment of inborn errors of the urea cycle

  1981cites this paper
• New approaches to the diagnosis and treatment of inborn errors or urea synthesis.

  1981cites this paper
• Comments on Dialysis Solution Composition, Antibiotic Transport, Poisoning, and Novel Uses of Peritoneal Dialysis

  1981cites this paper
• Antenatal diagnosis of defects of ureagenesis.

  1981cites this paper
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  1981cites this paper
• Carrier detection of urea cycle disorders.

  1981cites this paper
• Experience in two patients

  1980cites this paper
• Treatment of hyperammonemic inborn errors of urea synthesis coma caused by

  1980cites this paper
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  1980cites this paper
• Techniques for use of charcoal hemoperfusion in infants: experience in two patients.

  1980cites this paper
• Treatment of hyperammonemic coma caused by inborn errors of urea synthesis.

  1980cites this paper