Citrate therapy in argininosuccinate lyase deficiency

Author:

Iafolla A.K.,Gale D.S.,Roe C.R.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. New pathways of nitrogen excretion in inborn errors of urea synthesis;Brusilow;Lancet,1979

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

3. Therapy of urea cycle enzymopathies: three case studies;Batshaw;Johns Hopkins Med J,1981

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

5. Early dietary management of an infant with argininosuccinase deficiency: preliminary report;Shih;J Clin Invest,1972

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1. Anaplerotic therapy in propionic acidemia;Molecular Genetics and Metabolism;2017-09

2. Disorders of the Urea Cycle and Related Enzymes;Inborn Metabolic Diseases;2006

3. Considerations in the Difficult-to-Manage Urea Cycle Disorder Patient;Critical Care Clinics;2005-10

4. Management of Inherited Disorders of Ureagenesis;The Endocrinologist;2002-03

5. The nutritional management of urea cycle disorders;The Journal of Pediatrics;2001-01

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