(Q81539367)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

Brad Angle

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Barbara K Burton

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

publication date

31 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

1

1 reference

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9 January 2020

page(s)

36-39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency

9 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Electron transfer flavoprotein deficiency: functional and molecular aspects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Decreased activity of respiratory-chain enzymes in glutaric aciduria type II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

Tandem mass spectrometry in newborn screening. American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

D,L-3-hydroxybutyrate treatment of multiple acyl-CoA dehydrogenase deficiency (MADD)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.09.015

10.1016/J.YMGME.2007.09.015

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17977044%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference