(Q71853077)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6894281%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

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

1 reference

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21 October 2019

B H Robinson

1 reference

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21 October 2019

J Taylor

series ordinal

1 reference

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21 October 2019

S G Kahler

series ordinal

1 reference

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21 October 2019

H N Kirkman

series ordinal

1 reference

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21 October 2019

publication date

1 March 1981

1 reference

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European Journal of Pediatrics

21 October 2019

published in

1 reference

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21 October 2019

volume

136

1 reference

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21 October 2019

issue

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21 October 2019

page(s)

35-39

1 reference

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

21 October 2019

cites work

1 reference

12 December 2020

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

1 reference

12 December 2020

Two cases of phosphoenolpyruvate carboxykinase deficiency

1 reference

12 December 2020

A simplified method for the preparation of 14 C-labelled branched-chain -oxo acids

1 reference

12 December 2020

Regulation of renal gluconeogenesis by calcium ions, hormones and adenosine 3':5'-cyclic monophosphate

1 reference

12 December 2020

Lipoamide dehydrogenase in cultured human skin fibroblasts

1 reference

12 December 2020

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

1 reference

12 December 2020

Phosphoenolpyruvate carboxykinase and pyruvate carboxylase in developing rat liver

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hepatic fructose-1,6-diphosphatase deficiency. A cause of lactic acidosis and hypoglycemia in infancy

1 reference

12 December 2020

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

1 reference

12 December 2020

Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid, and purine abnormalities

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings

1 reference

12 December 2020

Studies on the Mechanism of Activation of Adipose Tissue Pyruvate Dehydrogenase by Insulin

1 reference

12 December 2020

Biochemical Genetics of the -Keto Acid Dehydrogenase Complexes of Escherichia coli K12: Isolation and Biochemical Properties of Deletion Mutants

1 reference

12 December 2020

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

12 December 2020

Subacute necrotizing encephalomyelopathy in an infant

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00441708

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6894281%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference

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