(Q37487716)

20 August 2017

Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop (English)

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20 August 2017

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Matthias R Baumgartner

5

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20 August 2017

U Spiekerkoetter

1

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20 August 2017

M Lindner

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20 August 2017

R Santer

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20 August 2017

M Grotzke

4

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20 August 2017

H Boehles

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20 August 2017

A Das

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20 August 2017

C Haase

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20 August 2017

J B Hennermann

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20 August 2017

D Karall

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20 August 2017

H de Klerk

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20 August 2017

I Knerr

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20 August 2017

H G Koch

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20 August 2017

B Plecko

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20 August 2017

W Röschinger

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20 August 2017

K O Schwab

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20 August 2017

D Scheible

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20 August 2017

F A Wijburg

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20 August 2017

J Zschocke

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20 August 2017

E Mayatepek

20

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20 August 2017

U Wendel

21

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20 August 2017

language of work or name

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28 April 2009

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Journal of Inherited Metabolic Disease

20 August 2017

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20 August 2017

32

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20 August 2017

4

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20 August 2017

498-505

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https://scigraph.springernature.com/pub.10.1007/s10545-009-1126-8

20 August 2017

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cites work

Management of fatty acid oxidation disorders: a survey of current treatment strategies

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12 December 2020

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

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12 December 2020

Screening newborns for inborn errors of metabolism by tandem mass spectrometry

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12 December 2020

Carnitine supplementation induces long-chain acylcarnitine production--studies in the VLCAD-deficient mouse

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12 December 2020

Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy

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12 December 2020

Carnitine supplementation induces acylcarnitine production in tissues of very long-chain acyl-CoA dehydrogenase-deficient mice, without replenishing low free carnitine

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12 December 2020

Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency

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12 December 2020

Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.

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12 December 2020

Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein.

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12 December 2020

MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency

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12 December 2020

Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship

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12 December 2020

Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency

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12 December 2020

Fuel utilization in patients with very long-chain acyl-coa dehydrogenase deficiency.

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12 December 2020

Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships

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12 December 2020

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

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12 December 2020

Effects of a fat load and exercise on asymptomatic VLCAD deficiency

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12 December 2020

Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

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12 December 2020

10.1007/S10545-009-1126-8

Identifiers

DOI

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20 August 2017

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