(Q43697393)

26 November 2017

title

Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementation (English)

1 reference

medium chain acyl-CoA dehydrogenase deficiency

26 November 2017

main subject

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author name string

W R Treem

series ordinal

1

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26 November 2017

C A Stanley

series ordinal

2

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26 November 2017

S I Goodman

series ordinal

3

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26 November 2017

publication date

1 January 1989

1 reference

Journal of Inherited Metabolic Disease

26 November 2017

published in

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26 November 2017

volume

12

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26 November 2017

issue

2

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26 November 2017

page(s)

112-119

1 reference

https://scigraph.springernature.com/pub.10.1007/bf01800712

26 November 2017

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800712

Carnitine deficiency, organic acidemias, and Reye's syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800712

Enzymic determination of D(-)-beta-hydroxybutyric acid and acetoacetic acid in blood

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800712

Hyperinsulinism in infancy: diagnosis by demonstration of abnormal response to fasting hypoglycemia

21 January 2018

1 reference

12 December 2020

L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Intracranial Pressure Elevations During Octanoate Infusion in Rabbits: an Experimental Model of Reye's Syndrome

1 reference

12 December 2020

COLORIMETRIC ULTRAMICRO METHOD FOR THE DETERMINATION OF FREE FATTY ACIDS

1 reference

12 December 2020

An improved and simplified radioisotopic assay for the determination of free and esterified carnitine

1 reference

12 December 2020

Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome.

1 reference

12 December 2020

Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.

1 reference

12 December 2020

Primary systemic carnitine deficiency. II. Renal handling of carnitine

1 reference

12 December 2020

Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.

1 reference

12 December 2020

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

1 reference

12 December 2020

L-carnitine therapy in isovaleric acidemia

1 reference

12 December 2020

Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts

1 reference

12 December 2020

Identification of long chain dicarboxylic acids in the serum of two patients with Reye's syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800712

1 reference

Dimensions Publication ID

26 November 2017

1049115168

0 references

1 reference