(Q52262628)

28 April 2018

title

Lacticacidaemia due to pyruvate dehydrogenase deficiency, with evidence of protein polymorphism in the alpha-subunit of the enzyme. (English)

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28 April 2018

author name string

N McKay

1

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28 April 2018

R Petrova-Benedict

2

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28 April 2018

J Thoene

3

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28 April 2018

B Bergen

4

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28 April 2018

W Wilson

5

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28 April 2018

B Robinson

6

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28 April 2018

publication date

1 February 1986

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28 April 2018

European Journal of Pediatrics

published in

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28 April 2018

volume

144

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28 April 2018

page(s)

445-450

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28 April 2018

issue

5

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28 April 2018

https://scigraph.springernature.com/pub.10.1007/bf00441736

exact match

0 references

cites work

Regulation of mammalian pyruvate dehydrogenase complex by a phosphorylation-dephosphorylation cycle

1 reference

12 December 2020

Spectrophotometric measurement of pyruvate dehydrogenase complex activity in cultured human fibroblasts

1 reference

12 December 2020

Phosphoenolpyruvate carboxykinase and pyruvate carboxylase in developing rat liver

1 reference

12 December 2020

Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

1 reference

12 December 2020

A defect in pyruvate decarboxylase in a child with an intermittent movement disorder

1 reference

12 December 2020

Intermittent ataxia with pyruvate-decarboxylase deficiency.

1 reference

12 December 2020

Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis

1 reference

12 December 2020

Pyruvate dehydrogenase complex activity in normal and deficient fibroblasts

1 reference

12 December 2020

Alpha-keto acid dehydrogenase complexes. XI. Comparative studies of regulatory properties of the pyruvate dehydrogenase complexes from kidney, heart, and liver mitochondria

1 reference

12 December 2020

The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis

1 reference

12 December 2020

Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase

1 reference

12 December 2020

The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency.

1 reference

12 December 2020

A kinetic study of dihydrolipoyl transacetylase from bovine kidney

1 reference

12 December 2020

Revised assays for the investigation of congenital lactic acidosis using 14C keto acids, eliminating problems associated with spontaneous decarboxylation

1 reference

12 December 2020

Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (leigh disease)

1 reference

12 December 2020

Enzymologic studies and therapy of Leigh's disease associated with pyruvate decarboxylase deficiency.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00441736

1 reference

28 April 2018

release_55uorcwqiffn3mpgqpqgaumrm4

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/55uorcwqiffn3mpgqpqgaumrm4

24 November 2022

mapped directly with Wikidata item

PubMed ID

3082638

1 reference

28 April 2018