(Q44536324)

3 December 2017

title

Adult presentation of MCAD deficiency revealed by coma and severe arrythmias (English)

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medium chain acyl-CoA dehydrogenase deficiency

3 December 2017

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author name string

F Feillet

1

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3 December 2017

G Steinmann

2

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3 December 2017

C Vianey-Saban

3

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3 December 2017

C de Chillou

4

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3 December 2017

N Sadoul

5

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3 December 2017

E Lefebvre

6

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3 December 2017

M Vidailhet

7

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3 December 2017

P E Bollaert

8

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3 December 2017

language of work or name

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1 August 2003

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3 December 2017

published in

Intensive Care Medicine

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3 December 2017

volume

29

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3 December 2017

issue

9

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3 December 2017

page(s)

1594-1597

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https://scigraph.springernature.com/pub.10.1007/s00134-003-1871-3

3 December 2017

exact match

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cites work

Oligodendrocytes use lactate as a source of energy and as a precursor of lipids

1 reference

12 December 2020

Relation between serum-free-fatty acids and arrhythmias and death after acute myocardial infarction

1 reference

12 December 2020

Ketogenic diet, amino acid metabolism, and seizure control

1 reference

12 December 2020

Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies

1 reference

12 December 2020

Postinfarction heart failure in rats is associated with upregulation of GLUT-1 and downregulation of genes of fatty acid metabolism.

1 reference

12 December 2020

Cross-sectional early mitral flow-velocity profiles from color Doppler in patients with mitral valve disease

1 reference

12 December 2020

Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in France

1 reference

12 December 2020

Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.

1 reference

12 December 2020

Physiological roles of ketone bodies as substrates and signals in mammalian tissues

1 reference

12 December 2020

Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis

1 reference

12 December 2020

A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evol

1 reference

12 December 2020

Metabolic disease and sudden, unexpected death in infancy

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12 December 2020

Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency

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12 December 2020

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

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12 December 2020

Brain Metabolism during Fasting*

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12 December 2020

Medium Chain Acyl-CoA Dehydrogenase Deficiency in Pennsylvania: Neonatal Screening Shows High Incidence and Unexpected Mutation Frequencies

1 reference

12 December 2020

[Model project for updating neonatal screening in Bavaria: concept and initial results]

1 reference

12 December 2020

Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman.

1 reference

12 December 2020

10.1007/S00134-003-1871-3

Identifiers

DOI

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3 December 2017

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