(Q41934686)

English

Lactic acidaemia

scientific article published on January 1984

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Lactic acidaemia (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

author name string

B H Robinson

1

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

W G Sherwood

2

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

publication date

1 January 1984

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

7 Suppl 1

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

69-73

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

https://scigraph.springernature.com/pub.10.1007/bf03047378

0 references

Subdural empyema in infants, children and adults

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

A possible mechanism for selective cerebellar damage in partial pyruvate dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

Abnormal activation of pyruvate dehydrogenase in Leigh disease fibroblasts.

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03047378

21 January 2018

The Development of Pyruvate Dehydrogenase in the Subhuman Primate <i>Macaca mulatta</i>

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactic acidosis due to pyruvate carboxylase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of pyruvate dehydrogenase kinase and phosphatase by acetyl-CoA/CoA and NADH/NAD ratios

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin activation of carboxylase activity in cultured fibroblasts from a child with a combined carboxylase defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyruvate Dehydrogenase Phosphatase Deficiency: A Cause of Congenital Chronic Lactic Acidosis in Infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermittent ataxia with pyruvate-decarboxylase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyruvate carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Defect in Branched-Chain Amino Acid Metabolism in a Patient with Congenital Lactic Acidosis due to Dihydrolipoyl Dehydrogenase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thiamin-responsive maple-syrup-urine disease: decreased affinity of the mutant branched-chain alpha-keto acid dehydrogenase for alpha-ketoisovalerate and thiamin pyrophosphate

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyruvate Carboxylase and Phosphoenolpyruvate Carboxykinase Activity in Leukocytes and Fibroblasts from a Patient with Pyruvate Carboxylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The activity of pyruvate dehydrogenase in rat brain during postnatal development

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATP-dependent inactivation of heart muscle pyruvate dehydrogenase and reactivation by Mg(++)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactic acidosis, neurological deterioration and compromised cellular pyruvate oxidation due to a defect in the reoxidation of cytoplasmically generated NADH.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inborn errors of pyruvate metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Clinical and Biochemical Implications of Pyruvate Carboxylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6434848

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03047378

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Dimensions Publication ID

0 references

release_nyu77d6oa5dzbmuymijgnxarze

1 reference

https://api.fatcat.wiki/v0/release/nyu77d6oa5dzbmuymijgnxarze

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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