(Q51568199)

7 April 2018

title

Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiency. (English)

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7 April 2018

author name string

Morris AA

1

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7 April 2018

Lascelles CV

2

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7 April 2018

Olpin SE

3

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7 April 2018

Lake BD

4

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7 April 2018

Leonard JV

5

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7 April 2018

Quant PA

6

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7 April 2018

language of work or name

English

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publication date

1 September 1998

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7 April 2018

published in

Pediatric Research

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7 April 2018

volume

44

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7 April 2018

issue

3

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7 April 2018

page(s)

392-396

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7 April 2018

https://scigraph.springernature.com/pub.10.1203/00006450-199809000-00021

exact match

0 references

cites work

Glucagon activates mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase in vivo by decreasing the extent of succinylation of the enzyme

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Amplification and direct sequencing of a cDNA encoding human cytosolic 3-hydroxy-3-methylglutaryl-coenzyme A synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Intercurrent illness in inborn errors of intermediary metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Treatment of rats with glucagon or mannoheptulose increases mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase activity and decreases succinyl-CoA content in liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Formation of ketone bodies by resting lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

Preferential utilization of ketone bodies for the synthesis of myelin cholesterol in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199809000-00021

10.1203/00006450-199809000-00021

21 January 2018

Identifiers

DOI

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7 April 2018

Dimensions Publication ID

1064213721

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1 reference

7 April 2018