(Q46889879)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Metabolic changes associated with hyperammonemia in patients with propionic acidemia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

author name string

Heather R Filipowicz

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Sharon L Ernst

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Carrie L Ashurst

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Marzia Pasquali

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

publication date

10 January 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

15 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

page(s)

123-130

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16406646%20AND%20SRC:MED&resulttype=core&format=json

The glutamine paradox in a neonate with propionic acidaemia and severe hyperammonaemia

15 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Failure of the normal ureagenic response to amino acids in organic acid-loaded rats. Proposed mechanism for the hyperammonemia of propionic and methylmalonic acidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

N-carbamylglutamate enhances ammonia detoxification in a patient with decompensated methylmalonic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

N-carbamylglutamate protects patients with decompensated propionic aciduria from hyperammonaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Abnormal gene expression causing hyperammonemia in carnitine-deficient juvenile visceral steatosis (JVS) mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Carnitine deficiency and hyperammonemia associated with valproic acid therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

The effect of carnitine supplementation in valproate-induced hyperammonaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Quantification of physiological amino acids by gradient ion-exchange high-performance liquid chromatography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Delta1-pyrroline-5-carboxylate synthase deficiency: neurodegeneration, cataracts and connective tissue manifestations combined with hyperammonaemia and reduced ornithine, citrulline, arginine and proline

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

N-acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Hepatic glutamine synthetase deficiency in fatal hyperammonemia after lung transplantation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Fatal hyperammonemia after orthotopic lung transplantation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Congenital glutamine deficiency with glutamine synthetase mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Alternative pathway therapy for urea cycle disorders: twenty years later

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Studies of hepatic glutamine metabolism in the perfused rat liver with (15)N-labeled glutamine.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Role of the glutamate dehydrogenase reaction in furnishing aspartate nitrogen for urea synthesis: studies in perfused rat liver with 15N.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Interorgan ammonia metabolism in liver failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

Hepatocyte Heterogeneity in the Metabolism of Amino Acids and Ammonia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.016

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1016/J.YMGME.2005.11.016

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/x5clm6pi2fg6pdtaxl5hlfrru4

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_x5clm6pi2fg6pdtaxl5hlfrru4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/x5clm6pi2fg6pdtaxl5hlfrru4

30 July 2022

mapped directly with Wikidata item

https://api.fatcat.wiki/v0/release/x5clm6pi2fg6pdtaxl5hlfrru4

1 reference

30 July 2022