Clinical Consequences of Urea Cycle Enzyme Deficiencies and Potential Links to Arginine and Nitric Oxide Metabolism

Author:

Scaglia Fernando1,Brunetti-Pierri Nicola1,Kleppe Soledad1,Marini Juan2,Carter Susan13,Garlick Peter2,Jahoor Farook4,O'Brien William1,Lee Brendan13

Affiliation:

1. Department of Molecular and Human Genetics, Children's Nutrition Research Center, Baylor College of Medicine

2. Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801

3. Howard Hughes Medical Institute, Houston, TX 77030

4. Department of Pediatrics, Children's Nutrition Research Center, Baylor College of Medicine

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Reference77 articles.

1. Urea cycle enzymes;Brusilow,1995

2. Cerebral dysfunction in asymptomatic carriers of ornithine transcarbamylase deficiency;Batshaw;N. Engl. J. Med.,1980

3. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea cycle enzymopathies;Msall;N. Engl. J. Med.,1984

4. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency;Maestri;Medicine (Baltimore),1998

5. Urea cycle disorders: diagnosis, pathophysiology, and therapy;Brusilow;Adv. Pediatr.,1996

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