(Q56688068)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

title

Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1 reference

N Amir

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

O N Elpeleg

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

R S Shalev

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

E Christensen

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

language of work or name

English

0 references

publication date

1 June 1989

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

4 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

volume

114

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

page(s)

983-989

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

Glutaric aciduria; A “new” disorder of amino acid metabolism

4 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria: Inherited deficiency of glutaryl-CoA dehydrogenase activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria: clinical and laboratory findings in two brothers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Intermittently Progressive Dyskinetic Syndrome in Glutaric Aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria type I presenting with hypoglycaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

L-carnitine treatment in glutaric aciduria type I.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria type 1: biochemical investigations and postmortem findings.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

A case of glutaric aciduria type I with unique abnormalities in the cerebral CT findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria: biochemical and morphologic considerations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Inhibition of brain glutamate decarboxylase by glutarate, glutaconate, and β-Hydroxyglutarate: Explanation of the symptoms in glutaric aciduria?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Lesions of the putamen: their relevance to dystonia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Evidence for transient perinatal glutamatergic innervation of globus pallidus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

A case of glutaric acidemia type I: effect of riboflavin and carnitine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Mitochondrial and peroxisomal metabolism of glutaryl-CoA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2889%2980442-1

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(89)80442-1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2723913%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1 reference