(Q70644633)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6489380%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6489380%20AND%20SRC:MED&resulttype=core&format=json

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

12 October 2019

main subject

0 references

1 reference

1 reference

W G Wilson

1

1 reference

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12 October 2019

M B Cass

2

1 reference

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12 October 2019

O Søvik

3

1 reference

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12 October 2019

K M Gibson

4

1 reference

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12 October 2019

L Sweetman

5

1 reference

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12 October 2019

publication date

1 September 1984

1 reference

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European Journal of Pediatrics

12 October 2019

published in

1 reference

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12 October 2019

volume

142

1 reference

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12 October 2019

issue

4

1 reference

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12 October 2019

page(s)

289-291

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00540255

12 October 2019

exact match

0 references

cites work

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

1 reference

12 December 2020

Idiopathic acute pancreatitis in children. Association with a clinical picture resembling Reye syndrome

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

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

1 reference

12 December 2020

Encephalopathy of Reye's syndrome: a review of pathogenetic hypotheses

1 reference

12 December 2020

Pancreatitis and Reye's Syndrome

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

The ultrasonic and biochemical diagnosis of pancreatitis in children

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

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

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

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

1 reference

12 December 2020

Letter: Idiopathic acute pancreatitis in children

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

Acute hemorrhagic pancreatitis and other visceral changes associated with acute encephalopathy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00540255

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6489380%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference