ARGININOSUCCINICACIDURIA: CLINICAL, METABOLIC AND DIETARY STUDY-Reference-Cited by-同舟云学术

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ARGININOSUCCINICACIDURIA: CLINICAL, METABOLIC AND DIETARY STUDY

Published:2008-06-28 Issue:1 Volume:18 Page:1-13
ISSN:0964-2633
Container-title:Journal of Intellectual Disability Research
language:en
Short-container-title:

Author:

BRENTON D. P.,CUSWORTH D. C.,HARTLEY SANDRA,LUMLEY SUSAN,KUZEMKO J. A.

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Neurology,Neurology,Arts and Humanities (miscellaneous),Rehabilitation

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.1974.tb01213.x/fullpdf

Reference13 articles.

1. A disease, probably hereditary, characterised by severe mental deficiency and a constant gross abnormality of amino acid metabolism;Allan;Lancet,1958

2. Renal clearances of amino acids in normal adults and in patients with aminoaciduria;Cusworth;Biochem. J.,1960

3. Determination of argininosuccinic acid by ion-exchange chromatography;Cusworth;Nature,1961

4. Improved method for the estimation of plasma ammonia by ion exchange;Fenton;J. Clin. Path.,1968

5. Argininosuccinic aciduria: an inborn error of amino acid metabolism;Levin;Arch. Dis. Childh.,1961

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