Santillán-Aguayo E, Revilla-Estivil N, LBelmont-Martínez L, Fernández-Lainez C, Guillén-López S, Ibarra-González I, Monroy-Santoyo S, Rodríguez-Schmidt R, Vela-Amieva M

Language: Spanish
References: 5
Page: 48-51
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REFERENCES

1. Fenton WA, Gravel RA, Rosenblatt DS. Disorders of Propionate and Methylmalonate Metabolism. En: Scriver CR, Beaudet AL, Sly WS, Valle D. The Metabolic & Molecular Bases of Inherited Disease, 8a Ed. USA: McGraw-Hill; 2001. p. 2165-93.

2. Wendel U, Ogier de Baulny H. Branched-Chain Organic Acidurias/ Acidemias. En: Fernandes J, Saudubray JM, Van den Berghe G, Walter JH. Inborn Metabolic Diseases, Diagnosis and Treatment, 4a Ed. Germany: Springer; 2006. p. 245-62.

3. Yannicelli S. Nutrition management of patients with inherited disorders of organic acid metabolism. En: Acosta P, Nutrition management of patients with inherited Metabolic Disorders. 1a. Ed. Sudbury MA: Jones and Bartlett Publishers; 2010. p. 283-308.

4. Deodato F, Boenzi S, Santorelli F, Dionisivici C. Methylmalonic and Propionic Aciduria. Am J Med Gen Part C 2006;142C:104-22.

5. Melo DR, Kowaltowski AJ, Wajner M, Castilho RF. Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia. J Bioenerg Biomembr 2011;43(1):39-46.