(Q67965469)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1886403%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

title

3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi Arabia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1886403%20AND%20SRC:MED&resulttype=core&format=json

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

20 September 2019

main subject

1 reference

1 reference

P T Ozand

1

1 reference

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20 September 2019

A al Aqeel

2

1 reference

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20 September 2019

G Gascon

3

1 reference

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20 September 2019

J Brismar

4

1 reference

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20 September 2019

E Thomas

5

1 reference

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20 September 2019

H Gleispach

6

1 reference

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20 September 2019

publication date

1 January 1991

1 reference

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Journal of Inherited Metabolic Disease

20 September 2019

published in

1 reference

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20 September 2019

volume

14

1 reference

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20 September 2019

issue

2

1 reference

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20 September 2019

page(s)

174-188

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01800590

20 September 2019

exact match

0 references

cites work

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

1 reference

12 December 2020

A double-isotope method for the measurement of ketone-body turnover in the rat. Effect of L-alanine

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-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patients

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new cases

1 reference

12 December 2020

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

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

Quantitative analysis for organic acids in biological samples: batch isolation followed by gas chromatographic-mass spectrometric analysis

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

3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review

1 reference

12 December 2020

Patient with Defect in Leucine Metabolism

1 reference

12 December 2020

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

1 reference

12 December 2020

CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients

1 reference

12 December 2020

A new case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency

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

Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800590

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1886403%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 September 2019

0 references

1 reference