(Q71228364)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

title

Glutaric acidemia type II: a form with deleterious intrauterine effects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference

S I Goodman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

M Reale

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

S Berlow

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

language of work or name

English

0 references

publication date

1 March 1983

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

17 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

volume

102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

page(s)

411-413

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

17 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Glutaric aciduria Type II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Glutaric acidemia type II: clinical, biochemical, and morphologic considerations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

New defect in fatty-acid metabolism with hypoglycemia and organic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Recurrent Hypoglycemia Associated with Glutaric Aciduria Type II in an Adult

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Organic aciduria in the riboflavin-deficient rat

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Mitochondrial proline dehydrogenase deficiency in hyperprolinemic PRO/Re mice: genetic and enzymatic analyses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980665-9

10.1016/S0022-3476(83)80665-9

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6681838%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference