(Q28332118)

1

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P M Coates

2

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D E Hale

3

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D S Millington

4

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R J Pollitt

5

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P Rinaldo

6

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C R Roe

7

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K Tanaka

Journal of Inherited Metabolic Disease

8

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language of work or name

English

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publication date

1990

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published in

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volume

13

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issue

5

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page(s)

707-15

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cites work

Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.

1 reference

12 December 2020

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.

1 reference

12 December 2020

Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine

1 reference

12 December 2020

The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Generalised dicarboxylic aciduria: a common finding in neonates

1 reference

12 December 2020

General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases

1 reference

12 December 2020

Application of fast atom bombardment with tandem mass spectrometry and liquid chromatography/mass spectrometry to the analysis of acylcarnitines in human urine, blood, and tissue

1 reference

12 December 2020

The incidence and presentation of dicarboxylic aciduria

1 reference

12 December 2020

Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death

1 reference

12 December 2020

Defects of metabolism of fatty acids in the sudden infant death syndrome

1 reference

12 December 2020

The enzymatic basis for the dehydrogenation of 3-phenylpropionic acid: in vitro reaction of 3-phenylpropionyl-CoA with various acyl-CoA dehydrogenases

1 reference

12 December 2020

Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome

1 reference

12 December 2020

Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes

1 reference

12 December 2020

Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring

1 reference

12 December 2020

Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

12 December 2020

Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver

1 reference

12 December 2020