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Prolonged N200 is the early neurophysiologic change in the patient with minimal hepatic encephalopathy
Hereditary diseases of coenzyme A thioester metabolism
Rizzon, P., Biasco, G., Di Biase, M., Boscia, F., Rizzo, U., Minafra, F., Bortone, A., Siliprandi, N., Procopio, A., Bagiella, E., and
Sima AAF, Calvani M, Mehra M, et al
Peebles et al., 2007) ayuda al embrin a utilizar esta fuente de energa
