(Q41180841)

27 September 2017

1 reference

title

Metabolic intermediates in lactic acidosis: compounds, samples and interpretation (English)

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27 September 2017

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F Poggi-Travert

1

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27 September 2017

D Martin

2

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27 September 2017

T Billette de Villemeur

3

1 reference

27 September 2017

J P Bonnefont

4

1 reference

27 September 2017

A Vassault

5

1 reference

27 September 2017

D Rabier

6

1 reference

27 September 2017

C Charpentier

7

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27 September 2017

P Kamoun

8

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27 September 2017

A Munnich

9

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27 September 2017

J M Saudubray

10

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27 September 2017

publication date

1 January 1996

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Journal of Inherited Metabolic Disease

27 September 2017

published in

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27 September 2017

volume

19

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27 September 2017

issue

4

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27 September 2017

page(s)

478-488

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https://scigraph.springernature.com/pub.10.1007/bf01799109

27 September 2017

exact match

0 references

cites work

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

Crossref

https://api.crossref.org/works/10.1007%2FBF01799109

Blood sampling technique for lactate and pyruvate estimation in children

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01799109

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

21 January 2018

1 reference

12 December 2020

Oral glucose lactate stimulation test in mitochondrial disease

1 reference

12 December 2020

Clinical aspects of mitochondrial disorders

1 reference

12 December 2020

Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings

1 reference

12 December 2020

Hepatic phosphorylase deficiency: Its differentiation from other hepatic glycogenoses

1 reference

12 December 2020

Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis

1 reference

12 December 2020

The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe

1 reference

12 December 2020

Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome.

1 reference

12 December 2020

Fructose load test—an in vivo screening test designed to assess pyruvate dehydrogenase activity and interconversion

1 reference

12 December 2020

Dichloroacetate as treatment for congenital lactic acidosis

1 reference

12 December 2020

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

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

Glycemic thresholds for activation of glucose counterregulatory systems are higher than the threshold for symptoms

1 reference

12 December 2020

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

12 December 2020

Blood sampling techniques for lactate and pyruvate estimation: a reappraisal

1 reference

12 December 2020

Neural dysfunction during hypoglycaemia

1 reference

12 December 2020

The dietary treatment of hepatic glycogen synthetase deficiency

1 reference

12 December 2020

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

12 December 2020

Metabolic fuel utilization and pyruvate oxidation during the postnatal period

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799109

1 reference

Dimensions Publication ID

27 September 2017

1000305203

0 references

1 reference