(Q70403389)

English

Compilation of gas chromatographic retention indices of 163 metabolically important organic acids, and their use in detection of patients with organic acidurias

scientific article published on 01 April 1982

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

Compilation of gas chromatographic retention indices of 163 metabolically important organic acids, and their use in detection of patients with organic acidurias (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

author name string

K Tanaka

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

D G Hine

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

publication date

1 April 1982

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

239

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

301-322

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7096501%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

Isovaleric acidemia: a new genetic defect of leucine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Jamaican vomiting sickness. Biochemical investigation of two cases

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The identification of tiglylglycine in the urine of a child with -methylcrotonylglycinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Identification of n-hexanoylglycine in urines from two patients with Jamaican vomiting sickness

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Identification of ethylmalonic acid in urine of two patients with the vomitting sickness of Jamaica

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

3-Hydroxypropionate: Significance of β-Oxidation of Propionate in Patients with Propionic Acidemia and Methylmalonic Acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Identification of β-hydroxyisovaleric acid in the urine of a patient with isovaleric acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The occurrence of β-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Gas chromatographic studies of twenty metabolically important acylglycines

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The identification of urinary acids by coupled gas chromatography-mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Quantitative analysis of branched-chain alpha-keto acids as their trimethylsilylated oximes

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Recurrent Hypoglycemia Associated with Glutaric Aciduria Type II in an Adult

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Clinical conditions associated with urinary excretion of 2-hydroxybutyric acid

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Metabolism of branched medium chain length fatty acid. I. Omega-oxidation of sodium dipropylacetate in rats

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Metabolism of branched medium chain length fatty acid. II--beta-oxidation of sodium dipropylacetate in rats

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Accumulation of 3-hydroxyisobutyric acid, 2-methyl-3-hydroxybutyric acid and 3-hydroxyisovaleric acid in ketoacidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Profiles in altered metabolism. I—The organic acids accumulating in acute non-diabetic ketoacidosis associated with alcoholism

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

A defect in l-isoleucine metabolism associated with alpha-methyl-beta-hydroxybutyric and alpha-methylacetoacetic aciduria: quantitative in vivo and in vitro studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

2-Ethylhydracrylic acid: a newly described urinary organic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Demonstration of a new mammalian isoleucine catabolic pathway yielding an Rseries of metabolites

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Human glycerol kinase deficiency with hyperglycerolemia and glyceroluria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Familial hyperglycerolemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Excretion of Propionylglycine in Propionic Acidaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

L-glyceric aciduria. A new genetic variant of primary hyperoxaluria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

D-Glyceric acidemia in a patient with chronic metabolic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Glutaric aciduria; presence of glutaconic and beta-hydroxyglutaric acids in urine

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The syndrome of systemic carnitine deficiency: Clinical, morphologic, biochemical, and pathophysiologic features

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The occurrence of adipic and suberic acid in urine from ketotic patients

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Pyroglutamic aciduria--a new inborn error of metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Increased pyroglutamic acid levels in patients on artificial diets

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Excretion of tiglyglycine in propionic acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

The identification and metabolic origin of 2-furoylglycine and 2,5-furandicarboxylic acid in human urine

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Alpha-ketoadipic aciduria: a description of a new metabolic error in lysine-tryptophan degradation

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

A gas-liquid-chromatographic procedure for separating a wide range of metabolites occuring in urine or tissue extracts

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9673%2800%2981990-1

7 January 2021

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q70403389&oldid=2176869618"