(Q28328775)

3-ethyl-3-methylpyruvic acid

ChEBI release 2020-05-28

ChEBI ID

82956

1 reference

ChEBI release 2020-05-28

H. Przyrembel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A759179

26 July 2022

H. J. Bremer

2

1 reference

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26 July 2022

M. Duran

3

1 reference

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26 July 2022

L. Bruinvis

4

1 reference

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26 July 2022

D. Ketting

5

1 reference

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26 July 2022

S. K. Wadman

6

1 reference

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26 July 2022

R. Baumgartner

7

1 reference

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26 July 2022

U. Irle

8

1 reference

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26 July 2022

C. Bachmann

9

1 reference

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European Journal of Pediatrics

26 July 2022

language of work or name

English

0 references

publication date

18 January 1979

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published in

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volume

130

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page(s)

1-14

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issue

1

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cites work

Tiglicaciduria in propionicacidaemia

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00441893

Isolation and Identification of Methylcitrate, a Major Metabolic Product of Propionate in Patients with Propionic Acidemia

21 January 2018

1 reference

12 December 2020

A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiency

1 reference

12 December 2020

13CValine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate

1 reference

12 December 2020

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

1 reference

12 December 2020

Combined carboxylase defect: biotin-responsiveness in cultured fibroblasts

1 reference

12 December 2020

The variability of metabolite excretion in propionicacidaemia

1 reference

12 December 2020

Propionicacidemia, a New Inborn Error of Metabolism

1 reference

12 December 2020

A "new" disorder of isoleucine catabolism

1 reference

12 December 2020

Quantitative gaschromatographic determination of short chain aldehydes and ketones in the urine of infants

1 reference

12 December 2020

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

1 reference

12 December 2020

Enzymic carboxylation of butyryl coenzyme A

1 reference

12 December 2020

Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.

1 reference

12 December 2020

Acute Neonatal Nonketotic Hyperglycinemia: Normal Propionate and Methylmalonate Metabolism

1 reference

12 December 2020

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

1 reference

12 December 2020

2-Ethylhydracrylic acid: a newly described urinary organic acid

1 reference

12 December 2020

Excretion of tiglyglycine in propionic acidemia

1 reference

12 December 2020

Propionic acidemia in patients with ketotic hyperglycinemia

1 reference

12 December 2020

Biotin-responsive beta-methylcrotonylglycinuria

1 reference

12 December 2020

Idiopathic hyperglycinemia: isolation and identification of three previously undescribed urinary ketones

1 reference

12 December 2020

Excretion of Propionylglycine in Propionic Acidaemia

1 reference

12 December 2020

The distribution of 17 carbon fatty acids in the liver of a child with propionicacidaemia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome"

1 reference

12 December 2020

Propionyl holocarboxylase synthesis. I. Preparation and properties of the enzyme system

1 reference

12 December 2020

Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.

1 reference

12 December 2020

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

12 December 2020

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria

1 reference

12 December 2020

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

1 reference

12 December 2020

Dimensions Publication ID

Identifiers

DOI

10.1007/BF00441893

0 references

1036394127

0 references