(Q69005857)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2443756%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

3-Hydroxy-3-methylglutaric aciduria: response to carnitine therapy and fat and leucine restriction (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2443756%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

author name string

M Dasouki

1

1 reference

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29 September 2019

D Buchanan

2

1 reference

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29 September 2019

N Mercer

3

1 reference

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29 September 2019

K M Gibson

4

1 reference

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29 September 2019

J Thoene

5

1 reference

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29 September 2019

publication date

1 January 1987

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2443756%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

29 September 2019

published in

1 reference

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29 September 2019

volume

10

1 reference

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29 September 2019

issue

2

1 reference

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29 September 2019

page(s)

142-146

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01800039

29 September 2019

exact match

0 references

cites work

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

1 reference

12 December 2020

Intracellular localization of the 3-hydroxy-3-methylglutaryl coenzme A cycle enzymes in liver. Separate cytoplasmic and mitochondrial 3-hydroxy-3-methylglutaryl coenzyme A generating systems for cholesterogenesis and ketogenesis

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

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

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

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

1 reference

12 December 2020

3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography

1 reference

12 December 2020

Patient with Defect in Leucine Metabolism

1 reference

12 December 2020

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

1 reference

12 December 2020

Diagnosis of organic acidemias by gas chromatography--mass spectrometry

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

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

3-Hydroxy-3-Methylglutaric Aciduria

1 reference

12 December 2020

Age-dependent excretion of 3-hydroxy-3-methylglutaric acid (HMG) and ketone bodies in the urine of full-term and pre-term newborns

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

Identifiers

DOI

10.1007/BF01800039

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2443756%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 September 2019

0 references

1 reference