Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria
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Elsevier BV
Reference27 articles.
1. New clinical phenotype of branched-chain acyl-CoA oxidation defect;Burlina;Lancet,1991
2. A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts;Burlina;J Pediatr,1994
3. Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency;García Silva;J Pediatr,1994
4. Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype;Garavaglia;J Inher Metab Dis,1994
5. Ethylmalonic aciduria: An organic acidemia with CNS involvement and vasculopathy;Ozand;Brain Dev,1994
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