(Q39592562)

13 September 2017

title

3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review (English)

1 reference

13 September 2017

S J Wysocki

1

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13 September 2017

R Hähnel

series ordinal

2

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13 September 2017

publication date

1 January 1986

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Journal of Inherited Metabolic Disease

13 September 2017

published in

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13 September 2017

volume

9

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13 September 2017

issue

3

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13 September 2017

page(s)

225-233

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Pyruvate Carboxylase Deficiency and Lactic Acidosis in a Retarded Child without Leigh's Disease

13 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01799652

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01799652

3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency: Postnatal management following prenatal diagnosis by analysis of maternal urine

21 January 2018

1 reference

12 December 2020

3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an infant with macrocephaly and mild metabolic acidosis

1 reference

12 December 2020

The consumption of fuels during prolonged starvation.

1 reference

12 December 2020

The determination of the biological value of dietary proteins. XVI. The minimum protein requirement of humans, tested with mixtures of whole egg plus potato and maize plus beans

1 reference

12 December 2020

Regulation of hepatic fatty acid oxidation and ketone body production

1 reference

12 December 2020

The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria

1 reference

12 December 2020

A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

Clinical and biochemical observations on a child with a deficiency of 3‐hydroxy‐3‐methylglutaryl coenzyme a lyase

1 reference

12 December 2020

3-Hydroxy-3-Methylglutaric, 3-Methylglutaconic and 3-Methylglutaric Acids can be Non-specific Indicators of Metabolic Disease

1 reference

12 December 2020

3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria

1 reference

12 December 2020

Patient with Defect in Leucine Metabolism

1 reference

12 December 2020

3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria

1 reference

12 December 2020

3-Hydroxy-3-methylglutaric aciduria: 3-hydroxy-3-methylglutaryl-coenzyme A lyase levels in leucocytes

1 reference

12 December 2020

Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousins

1 reference

12 December 2020

Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts

1 reference

12 December 2020

L-Carnitine Insufficiency in Disorders of Organic acid Metabolism: Response to L-Carnitine by Patients with Methylmalonic Aciduria and 3-Hydroxy-3-methylglutaric Aciduria

1 reference

12 December 2020

Brain Metabolism during Fasting*

1 reference

12 December 2020

3-Hydroxy-3-Methylglutaric Aciduria

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency. Follow-up of first described case

1 reference

12 December 2020

Hyperammonaemia and urinary organic acids

1 reference

12 December 2020

Amino Acid Metabolism in Man

1 reference

12 December 2020

beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome

1 reference

12 December 2020

3-Hydroxy-3-methylglutaric aciduria: deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase

1 reference

12 December 2020

Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799652

1 reference

release_jhul2knnifh6tbjanttxxejk6m

13 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jhul2knnifh6tbjanttxxejk6m

24 November 2022

mapped directly with Wikidata item

1 reference