(Q73079652)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

J L Van Hove

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

S G Kahler

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

M D Feezor

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J P Ramakrishna

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

P Hart

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

W R Treem

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J J Shen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

D Matern

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

D S Millington

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

publication date

1 September 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

1 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

571-582

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11032332%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1005673828469

1 November 2019

exact match

0 references

1 reference

12 December 2020

Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry

1 reference

12 December 2020

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

1 reference

12 December 2020

Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method.

1 reference

12 December 2020

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

1 reference

12 December 2020

Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

2 references

12 December 2020

Crossref

https://api.crossref.org/works/10.1023%2FA%3A1005673828469

7 January 2021

inferred from DOI database lookup

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

1 reference

12 December 2020

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

1 reference

12 December 2020

The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

1 reference

12 December 2020

Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometry

1 reference

12 December 2020

beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria

1 reference

12 December 2020

3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis.

1 reference

12 December 2020

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

1 reference

12 December 2020

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.

1 reference

12 December 2020

Quantitative acylcarnitine profiling in fibroblasts using [U-13C] palmitic acid: an improved tool for the diagnosis of fatty acid oxidation defects

1 reference

12 December 2020

Propionylcarnitine physiological variations in vivo

1 reference

12 December 2020

Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disorders

1 reference

12 December 2020

The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disorders

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

1 reference

12 December 2020

Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

1 reference

12 December 2020

Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient

1 reference

12 December 2020