(Q47757952)

5 February 2018

review article

1 reference

title

Alternative pathway therapy for urea cycle disorders (English)

1 reference

5 February 2018

author name string

F Feillet

series ordinal

1

1 reference

5 February 2018

J V Leonard

series ordinal

2

1 reference

5 February 2018

publication date

1 January 1998

1 reference

5 February 2018

Journal of Inherited Metabolic Disease

published in

1 reference

5 February 2018

volume

21 Suppl 1

1 reference

5 February 2018

page(s)

101-111

1 reference

5 February 2018

Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency

cites work

1 reference

12 December 2020

Increased tryptophan uptake into the brain in hyperammonemia

1 reference

12 December 2020

The biochemistry and toxicology of benzoic acid metabolism and its relationship to the elimination of waste nitrogen

1 reference

12 December 2020

Effect of single oral dose of sodium benzoate on ureagenesis in healthy men and two patients with late onset citrullinaemia

1 reference

12 December 2020

Effect of sodium benzoate on cerebral and hepatic energy metabolites in spf mice with congenital hyperammonemia

1 reference

12 December 2020

Brain uptake of tryptophan in urease-injected hyperammonemic rats after treatment with benzoate or hippurate

1 reference

12 December 2020

Inhibition of pyruvate carboxylase by sequestration of coenzyme A with sodium benzoate

1 reference

12 December 2020

Evidence of lack of toxicity of sodium phenylacetate and sodium benzoate in treating urea cycle enzymopathies

1 reference

12 December 2020

Effect of L-carnitine on cerebral and hepatic energy metabolites in congenitally hyperammonemic sparse-fur mice and its role during benzoate therapy

1 reference

12 December 2020

Carbamyl glutamate prevents the potentiation of ammonia toxicity by sodium benzoate

1 reference

12 December 2020

Disposition of Phenylbutyrate and its Metabolites, Phenylacetate and Phenylacetylglutamine

1 reference

12 December 2020

Urea cycle disorders: diagnosis, pathophysiology, and therapy.

1 reference

12 December 2020

Prospective treatment of urea cycle disorders.

1 reference

12 December 2020

Long-term treatment of girls with ornithine transcarbamylase deficiency

1 reference

12 December 2020

New pathways of nitrogen excretion in inborn errors of urea synthesis

1 reference

12 December 2020

The arginine requirement of the infant

1 reference

12 December 2020

Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia.

1 reference

12 December 2020

Waste nitrogen excretion via amino acid acylation: benzoate and phenylacetate in lysinuric protein intolerance

1 reference

12 December 2020

Sodium benzoate inhibits fatty acid oxidation in rat liver: effect on ammonia levels

1 reference

12 December 2020

Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis

1 reference

12 December 2020

Chronic benzoate therapy in a boy with partial ornithine transcarbamylase deficiency

1 reference

12 December 2020

Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy

1 reference

12 December 2020

Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis

1 reference

12 December 2020

Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies

1 reference

12 December 2020

Long-term survival of patients with argininosuccinate synthetase deficiency.

1 reference

12 December 2020

Phenylacetylglutamine May Replace Urea as a Vehicle for Waste Nitrogen Excretion

1 reference

12 December 2020

Arginine deficiency syndrome. Its occurrence in carbamyl phosphate synthetase deficiency

1 reference

12 December 2020

Amino acids in the rat liver and plasma and some metabolites in the liver after sodium benzoate treatment

1 reference

12 December 2020

Plasma glutamine concentration: A guide in the management of urea cycle disorders

1 reference

12 December 2020

Magnetic resonance spectroscopy shows increased brain glutamine in ornithine carbamoyl transferase deficiency

1 reference

12 December 2020

Behavior management of feeding disturbances in urea cycle and organic acid disorders

1 reference

12 December 2020

Hypocarnitinemia in patients affected by a primary defect of ammonia metabolism treated with sodium benzoate

1 reference

12 December 2020

Arginine therapy of argininosuccinase deficiency

1 reference

12 December 2020

Acute metabolic encephalopathy: a review of causes, mechanisms and treatment

1 reference

12 December 2020

Dose-dependent pharmacokinetics of benzoic acid following oral administration of sodium benzoate to humans

1 reference

12 December 2020

The potentiation of ammonia toxicity by sodium benzoate is prevented by L-carnitine

1 reference

12 December 2020

Effect of long-term administration of sodium benzoate to a patient with partial ornithine carbamoyl transferase deficiency

1 reference

12 December 2020

Availability of glycine and coenzyme A limits glycine conjugation in vivo

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005365825875

1 reference

5 February 2018

Dimensions Publication ID

1040689353

0 references

1 reference

5 February 2018