(Q51641826)

8 April 2018

title

Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities. (English)

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8 April 2018

author name string

M Duran

1

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8 April 2018

J B de Klerk

2

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8 April 2018

S K Wadman

3

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8 April 2018

H R Scholte

4

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8 April 2018

R P Beekman

5

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8 April 2018

F G Jennekens

6

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8 April 2018

publication date

1 August 1984

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8 April 2018

European Journal of Pediatrics

published in

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8 April 2018

volume

142

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8 April 2018

issue

3

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8 April 2018

page(s)

224-228

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8 April 2018

https://scigraph.springernature.com/pub.10.1007/bf00442456

exact match

0 references

cites work

Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to age.

1 reference

12 December 2020

Fatal cases of lipid storage myopathy with carnitine deficiency

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12 December 2020

Systemic carnitine deficiency simulating recurrent Reye syndrome.

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Gas chromatography of urinary N-phenylacetylglutamine

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12 December 2020

Multiple acyl-Co A dehydrogenation deficiency (MADD) in a boy with nonketotic hypoglycemia, hepatomegaly, muscle hypotonia and cardiomyopathy. Detection of N-isovalerylglutamic acid and its monoamide.

1 reference

12 December 2020

Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

1 reference

12 December 2020

Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase

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12 December 2020

Hypoketosis as a cause of symptoms in childhood hypoglycemia.

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12 December 2020

Medium-chain triglyceride medication as a pitfall in the diagnosis of non-ketotic C6-C10-dicarboxylic acidurias

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12 December 2020

Carnitine metabolism in normal-weight and obese human subjects during fasting

1 reference

12 December 2020

Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case

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12 December 2020

The syndrome of systemic carnitine deficiency: Clinical, morphologic, biochemical, and pathophysiologic features

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12 December 2020

Profiles in altered metabolism. II--(omega -- 1)-hydroxyacid excretion in a case of episodic hypoglycemia

1 reference

12 December 2020

C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects

1 reference

12 December 2020

Familial carnitine deficiency. A fatal case and subclinical state in a sister

1 reference

12 December 2020

Plasma and Urine Carnitine in Diabetic Ketosis

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12 December 2020

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats

1 reference

12 December 2020

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

12 December 2020

Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation.

1 reference

12 December 2020

An accurate and sensitive assay of long-chain fatty acid oxidation in human skeletal muscle

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00442456

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8 April 2018

PubMed ID

6468448

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8 April 2018