(Q51666740)

9 April 2018

title

Dicarboxylic aminoaciduria: an inborn error of amino acid conservation. (English)

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9 April 2018

dicarboxylic aminoaciduria

main subject

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2

Dallaire L

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9 April 2018

Serge B. Melançon

1

object named as

Melançon SB

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9 April 2018

author name string

Lemieux B

3

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9 April 2018

Robitaille P

4

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9 April 2018

Potier M

5

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9 April 2018

language of work or name

English

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publication date

1 September 1977

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9 April 2018

The Journal of Pediatrics

published in

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9 April 2018

volume

91

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9 April 2018

issue

3

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9 April 2018

page(s)

422-427

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9 April 2018

Dicarboxylic aminoaciduria: an inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia.

cites work

1 reference

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Urinary phenolic acids in tyrosinemia. identification and quantitation by gas chromatographymass spectrometry

7 January 2021

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Branched-chain alpha-keto acids isolated as oxime derivatives: relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease

7 January 2021

1 reference

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A defect in pyruvate decarboxylase in a child with an intermittent movement disorder

7 January 2021

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Use of a "heparin lock" in the intermittent administration of intravenous drugs. A technical advance in intravenous therapy

7 January 2021

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The free amino acids of human spinal fluid determined by ion exchange chromatography.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

Effect of infusion of single amino acids upon excretion of other amino acids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

The Renal Clearance of Amino Acids in Cystinuria*

7 January 2021

1 reference

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Microinjections of L-leucine into tubules and peritubular capillaries of the rat. II. The maleic acid model

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

Metabolic Studies of a Family with Massive Formiminoglutamic Aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

A SEX-LINKED DISORDER WITH MENTAL AND PHYSICAL RETARDATION CHARACTERIZED BY CEREBROCORTICAL ATROPHY AND INCREASE OF GLUTAMIC ACID IN THE CEREBROSPINAL FLUID.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

Cystinuria: biochemical evidence for three genetically distinct diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2877%2981312-7

10.1016/S0022-3476(77)81312-7

7 January 2021

Identifiers

DOI

1 reference

9 April 2018

1 reference

9 April 2018