(Q54193853)

26 May 2018

title

Localisation of enzymic defect in propionicacidaemia. (English)

1 reference

26 May 2018

author name string

D Gompertz

1

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26 May 2018

C N Storrs

2

1 reference

26 May 2018

D C Bau

3

1 reference

26 May 2018

T J Peters

4

1 reference

26 May 2018

E A Hughes

5

1 reference

26 May 2018

language of work or name

English

0 references

publication date

1 May 1970

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26 May 2018

published in

The Lancet

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26 May 2018

volume

1

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26 May 2018

issue

7657

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26 May 2018

page(s)

1140-1143

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26 May 2018

Congenital methylmalonic acidemia: enzymatic evidence for two forms of the disease

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1 reference

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7 January 2021

Propionicacidemia, a New Inborn Error of Metabolism

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https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Isovaleric acidemia: a new genetic defect of leucine metabolism

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7 January 2021

The measurement of urinary methylmalonic acid by a combination of thin-layer and gas chromoatography

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7 January 2021

The intracellular and intramitochondrial distribution of malonyl-CoA decarboxylase and propionyl-CoA carboxylase in rat liver.

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7 January 2021

Methylmalonyl CoA as an abnormal substrate for δ-aminolevulinic acid synthetase

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7 January 2021

A versatile lithium buffer elution system for single column automatic amino acid chromatography

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7 January 2021

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

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7 January 2021

HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.

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7 January 2021

Human erythrocyte phosphoglycerides. I. Quantification of plasmalogens, fatty acids and fatty aldehydes

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https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

PHOSPHOLIPID AND FATTY ACID CHARACTERISTICS OF ERYTHROCYTES IN SOME CASES OF ANAEMIA.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Methylmalonic acidemia. A disorder associated with acidosis, hyperglycinemia, and hyperlactatemia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Observations on the coexistence of methylmalonic acidemia and glycinemia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Defective propionate carboxylation in ketotic hyperglycinaemia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

Aminoacetone formation by Staphylococcus aureus

1 reference

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7 January 2021

Fatty acid desaturase systems of hen liver and their inhibition by cyclopropene fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2870%2991216-X

7 January 2021

10.1016/S0140-6736(70)91216-X

Identifiers

DOI

1 reference

26 May 2018

1 reference

26 May 2018