Improving Treatment of Guanidinoacetate Methyltransferase Deficiency: Reduction of Guanidinoacetic Acid in Body Fluids by Arginine Restriction and Ornithine Supplementation
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference23 articles.
1. Guanidinoacetate methyltransferase deficiency: The first inborn error of creatine metabolism in man;Stöckler;Am J Hum Genet,1996
2. Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: Diagnostic tools for a new inborn error of metabolism;Schulze;J Pediatr,1997
3. Creatine deficiency in the brain: A new, treatable inborn error of metabolism;Stöckler;Pediatr Res,1994
4. Guanidinoacetate methyltransferase deficiency: New clinical features;Ganesan;Pediatr Neurol,1997
5. Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism;Stöckler;Lancet,1996
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