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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, ...
Lactate dehydrogenase activity is inhibited by methylmalonate in vitro
(Springer/plenum PublishersNew YorkEUA, 2006)
Acidemia Metilmalónica: presentación de un caso y revisión de la literatura científica
(Universidad Militar Nueva Granada, 2014)
O papel da amônia sobre as alterações comportamentais, neuroinflamação e apoptose em um modelo experimental de acidemia metilmalônica.
(Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em FarmacologiaCentro de Ciências da Saúde, 2017-08-29)
Methylmalonic acidemia is an autosomal recessive metabolism biochemically characterized by
a deficiency in the activity of the mutase methylmalonyl-CoA and the tissue accumulation of
methylmalonate (MMA). In this acidemia, ...