Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency (Q68276775)

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23 September 2019

title

Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3346778%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

author name string

Y Ohtani

1

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23 September 2019

K Ohyanagi

2

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23 September 2019

S Yamamoto

3

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23 September 2019

I Matsuda

4

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23 September 2019

language of work or name

English

0 references

publication date

1 March 1988

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The Journal of Pediatrics

23 September 2019

published in

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23 September 2019

volume

112

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23 September 2019

page(s)

409-414

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23 September 2019

issue

3

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Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion

23 September 2019

cites work

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

7 January 2021

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Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency

7 January 2021

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Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency.

7 January 2021

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Partial ornithine transcarbamylase deficiency simulating Reye syndrome

7 January 2021

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Biochemical heterogeneity of ornithine carbamoyl transferase(OCT) in patients with OCT deficiency

7 January 2021

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Carnitine metabolism and inborn errors

7 January 2021

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Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine

7 January 2021

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Carnitine deficiency, organic acidemias, and Reye's syndrome

7 January 2021

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Carnitine status in Reye and Reye-like syndromes

7 January 2021

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Renal handling of carnitine in children with carnitine deficiency and hyperammonemia associated with valproate therapy

7 January 2021

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Application of high resolution fast atom bombardment and constant B/E ratio linked scanning to the identification and analysis of acylcarnitines in metabolic disease

7 January 2021

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Primary systemic carnitine deficiency. II. Renal handling of carnitine

7 January 2021

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Urea cycle regulation: I. Coupling of ornithine metabolism to mitochondrial oxidative phosphorylation

7 January 2021

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Sodium valproate and ornithine carbamyl transferase deficiency

7 January 2021

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Evidence of inherited urea cycle defect in a case of fatal valproate toxicity

7 January 2021

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Valproate toxicity and ornithine carbamoyltransferase deficiency

7 January 2021

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Inhibitory effects of sodium valproate on oxidative phosphorylation

7 January 2021

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Carnitine deficiency and hyperammonemia associated with valproic acid therapy

7 January 2021

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Mitochondrial abnormalities of liver in primary ornithine transcarbamylase deficiency

7 January 2021

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Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups

7 January 2021

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Carnitine prevents Reye-like syndrome in atypical carnitine deficiency.

7 January 2021

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Effects of L-carnitine on urea synthesis following acute ammonia intoxication in mice

7 January 2021

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Protective effect of L-carnitine on hyperammonemia

7 January 2021

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Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

7 January 2021

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10.1016/S0022-3476(88)80321-4

7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3346778%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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