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Journal Abstract Search

109 related items for PubMed ID: 5101292

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  • 4. Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.
    Przyrembel H, Bremer HJ, Duran M, Bruinvis L, Ketting D, Wadman SK, Baumgartner R, Irle U, Bachmann C.
    Eur J Pediatr; 1979 Jan 18; 130(1):1-14. PubMed ID: 759179
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  • 14. Dysautonomia in an infant with secondary hyperammonemia due to propionyl coenzyme A carboxylase deficiency.
    Harris DJ, Yang BI, Wolf B, Snodgrass PJ.
    Pediatrics; 1980 Jan 18; 65(1):107-10. PubMed ID: 7355003
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  • 15. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
    Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA.
    Mol Genet Metab; 2006 Aug 18; 88(4):327-33. PubMed ID: 16697227
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  • 16. Propionate increases neuronal histone acetylation, but is metabolized oxidatively by glia. Relevance for propionic acidemia.
    Nguyen NH, Morland C, Gonzalez SV, Rise F, Storm-Mathisen J, Gundersen V, Hassel B.
    J Neurochem; 2007 May 18; 101(3):806-14. PubMed ID: 17286595
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  • 17. [Non-ketotic hyperglycinemia. Presentation of a case].
    Mignone F, Balbo L, Valpreda A, Sciolla N, Chiappo GF, Bonetti G.
    Minerva Pediatr; 1980 Jan 31; 32(2):111-7. PubMed ID: 7382930
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  • 19. Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment.
    Wolf B, Hsia YE, Sweetman L, Feldman G, Boychuk RB, Bart RD, Crowell DH, Di Mauro RM, Nyhan WL.
    Pediatrics; 1981 Jul 31; 68(1):113-8. PubMed ID: 6787561
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  • 20. Activation of propionyl-CoA carboxylase in skin fibroblasts from a patient with propionicacidemia.
    Wong PW, Justice P, Reyes L, Hsia DY.
    J Lab Clin Med; 1971 Dec 31; 78(6):1004. PubMed ID: 5131830
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