Argininosuccinic aciduria: Investigation of an affected family-Reference-Cited by-同舟云学术

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Argininosuccinic aciduria: Investigation of an affected family

Published:1974-01 Issue:1 Volume:84 Page:85-89
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Billmeier Gerard J.,Molinary Samuel V.,Wilroy R.S.,Duenas Danilo A.,Brannon M. Elizabeth

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver;Brown;J. Biol. Chem.,1959

2. Urea cycle disorders;Shih,1971

3. Argininosuccinic aciduria;Maagoe;Danish Med. Bull.,1969

4. Early dietary management in an infant with argininosuccinase dieficiency;Shih;J. Pediatr.,1972

5. Selected screening tests for genetic metabolic diseases;Howell,1969

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Aciduria argininosuccínica: informe de un caso de inicio neonatal;Archivos Argentinos de Pediatria;2021-10-01

2. Liver involvement in urea cycle disorders: a review of the literature;Journal of Inherited Metabolic Disease;2017-09-12

3. Argininosuccinic aciduria: from a monogenic to a complex disorder;Genetics in Medicine;2013-04

4. Optimizing therapy for argininosuccinic aciduria;Molecular Genetics and Metabolism;2012-09

5. Argininosuccinate lyase deficiency;Genetics in Medicine;2012-05

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