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Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia
(SPRINGER/PLENUM PUBLISHERS, 2011)
Methylmalonic acidemia is one of the most prevalent inherited metabolic disorders involving neurological deficits. In vitro experiments, animal model studies and tissue analyses from human patients suggest extensive ...
Papel da óxido nítrico sintase induzível no córtex cerebral de modelos experimentais da acidemia metilmalônica
(Universidade Federal de Santa MariaBRBioquímicaUFSMPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica, 2012-12-15)
Methylmalonic acidemia is an inborn error of metabolism characterized clinically and biochemically by
tissue accumulation of methylmalonic acid (MMA) and neurological dysfunction, including convulsion.
Furthermore, ...
llex paraguariensis e seus componentes majoritários atenuam as alterações comportamentais, mortalidade e nos parâmetros bioquímicos associados a exposição ao malonato ou metilmalonato em Drosophila melonogasterllex paraguariensis and major components attenuate behavioral changes, mortality and biochemical parameters associated with exposure to malonate or methylmalonate in Drosophila melanogaster
(Universidade Federal do PampaUNIPAMPADoutorado em BioquímicaBrasilCampus Uruguaiana, 2021)
Acidemia Metilmalónica: presentación de un caso y revisión de la literatura científica
(Universidad Militar Nueva Granada, 2014)
Lactate dehydrogenase activity is inhibited by methylmalonate in vitro
(Springer/plenum PublishersNew YorkEUA, 2006)
Dificuldades no diagnostico e manejo da acidemia metilmalônica - relato de caso sugestivoDifficulties in diagnosis and treatment of methylmalonic aciduria - suggestive case report
(Sociedade de Pediatria do Estado do Rio de Janeiro, 2015)
Acidemia Metilmalónica: presentación de un caso y revisión de la literatura científica
(Universidad Militar Nueva Granada, 2014)