Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
about
Life extension in Drosophila by feeding a drug.Advances in urea cycle neuroimaging: Proceedings from the 4th International Symposium on urea cycle disorders, Barcelona, Spain, September 2013Carcinogenic effects in a phenylketonuria mouse modelRapidly fatal hyperammonemic coma in adults. Urea cycle enzyme deficiencySelective growth arrest and phenotypic reversion of prostate cancer cells in vitro by nontoxic pharmacological concentrations of phenylacetate.Modifying histones to tame cancer: clinical development of sodium phenylbutyrate and other histone deacetylase inhibitors.Orthotopic liver transplantation for ornithine transcarbamylase deficiency with hyperammonemic encephalopathy.Orthotopic liver transplantation for urea cycle enzyme deficiencyIn vivo urea cycle flux distinguishes and correlates with phenotypic severity in disorders of the urea cycle.Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locusHepatocyte gene therapy in a large animal: a neonatal bovine model of citrullinemiaThe glycine deportation system and its pharmacological consequences.Profile of Circulatory Metabolites in a Relapsing-remitting Animal Model of Multiple Sclerosis using Global Metabolomics.In vivo nitrogen metabolism in ornithine transcarbamylase deficiency.Noncirrhotic hyperammonaemic encephalopathy.Starvation response in mouse liver shows strong correlation with life-span-prolonging processes.Biochemical relationships between Reye's and Reye's-like metabolic and toxicological syndromes.Nutritional therapy for selected inborn errors of metabolism.Effect of pantothenic acid on hippurate formation in sodium benzoate-treated HepG2 cells.Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review.Saline is as effective as nitrogen scavengers for treatment of hyperammonemia.Inhibition of estrogen-dependent breast cell responses with phenylacetate.Brain edema and intracranial hypertension in fulminant hepatic failure: pathophysiology and management.Phenylacetate pharmacokinetics based on iterative two-stage population analysis.Hepatic uptake and metabolism of benzoate: a multiple indicator dilution, perfused rat liver study.The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency.Disposition of phenylbutyrate and its metabolites, phenylacetate and phenylacetylglutamine.Lysine benzoylation is a histone mark regulated by SIRT2
P2860
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P2860
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
description
1984 nî lūn-bûn
@nan
1984 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@ast
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@en
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@nl
type
label
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@ast
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@en
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@nl
prefLabel
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@ast
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@en
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@nl
P2093
P1476
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis
@en
P2093
C McKeethren
L Levitsky
S W Brusilow
P304
P356
10.1056/NEJM198406213102503
P407
P577
1984-06-21T00:00:00Z