Clinical Features and Neurologic Progression of Hyperargininemia

Author:

Carvalho Daniel R.,Brum Jaime M.,Speck-Martins Carlos E.,Ventura Fabrício D.,Navarro Mônica M.M.,Coelho Kátia E.F.A.,Portugal Dalton,Pratesi Riccardo

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Argininemia: A treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: Case reports and literature review;Prasad;J Child Neurol,1997

2. Hyperargininemia due to liver arginase deficiency;Crombez;Mol Genet Metab,2005

3. Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency;Scaglia;Am J Med Genet [C] Semin Med Genet,2006

4. Hyperargininemia: A treatable inborn error of metabolism?;De Deyn,1997

5. Cederbaum SD, Crombez EA. Arginase deficiency. GeneReviews. Seattle: University of Washington. Available at: http://www.ncbi.nlm.nih.gov/pubmed/20301338. Updated October 5, 2010.

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