Inherited Metabolic Disease in the Newborn: Approach to Diagnosis and Treatment-Reference-Cited by-同舟云学术

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Inherited Metabolic Disease in the Newborn: Approach to Diagnosis and Treatment

Published:1986 Issue:1 Volume:33 Page:197-223
ISSN:0065-3101
Container-title:Advances in Pediatrics
language:en
Short-container-title:Advances in Pediatrics

Author:

Goodman Stephen I.

Publisher

Elsevier BV

Reference62 articles.

1. GC-MS and the inherited organic acidemias;Goodman;Am J Hum Genet,1980

2. Neonatal hyperammonemic coma;Brusilow;Adv Pediatr,1982

3. Treatment of inborn errors of urea synthesis: Activation of alternative pathways of waste nitrogen synthesis and excretion;Batshaw;N Engl J Med,1982

4. Treatment of hyperammonemic coma caused by inborn errors of urea synthesis;Batshaw;J Pediatr,1980

5. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis;Brusilow;J Clin Invest,1984

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