(Q41896512)

English

Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: effect of metabolic state and L-carnitine therapy

scientific article published on October 1989

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scholarly article

1 reference

Europe PubMed Central

13 October 2017

Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: effect of metabolic state and L-carnitine therapy (English)

1 reference

Europe PubMed Central

13 October 2017

author name string

Schmidt-Sommerfeld E

1

1 reference

Europe PubMed Central

13 October 2017

Penn D

2

1 reference

Europe PubMed Central

13 October 2017

Kerner J

3

1 reference

Europe PubMed Central

13 October 2017

Bieber LL

4

1 reference

Europe PubMed Central

13 October 2017

Rossi TM

5

1 reference

Europe PubMed Central

13 October 2017

Lebenthal E

6

1 reference

Europe PubMed Central

13 October 2017

language of work or name

0 references

publication date

1 October 1989

1 reference

Europe PubMed Central

13 October 2017

The Journal of Pediatrics

1 reference

Europe PubMed Central

13 October 2017

115

1 reference

Europe PubMed Central

13 October 2017

577-582

1 reference

Europe PubMed Central

13 October 2017

4

1 reference

Europe PubMed Central

13 October 2017

In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

A radioisotopic-exchange method for quantitation of short-chain (acid-soluble) acylcarnitines

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Hypoketosis as a cause of symptoms in childhood hypoglycemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Carnitine plasma concentrations in 353 metabolically healthy children.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Analysis of acylcarnitines in normal human urine with the radioisotopic exchange-high performance liquid chromatography (HPLC) method

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Short-chain acylcarnitines: identification and quantitation

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Primary systemic carnitine deficiency. II. Renal handling of carnitine

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

Isolation and identification of alpha-methyloctanylcarnitines from human urine

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Propionylcarnitine physiological variations in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980284-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0022-3476(89)80284-7

1 reference

Europe PubMed Central

13 October 2017

1 reference

Europe PubMed Central

13 October 2017

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