A rare inborn error of metabolism disorder with early-onset acute encephalopathic episodes (frequently triggered by viral infections) associated with lactic acidosis and alpha-ketoglutaric aciduria which typically manifest with variable degrees of at

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encéphalopathie de l'enfant par déficit en thiamine pyrophosphokinase

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sub-acute ruminal acidosis [ SARA | chronic acidosis | sub-clinical acidosis ]

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acidose ruminale chronique [ ARC | acidose ruminale subaiguë | acidose latente ]

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A rare inherited mitochondrial disorder due to a defect in mitochondrial protein synthesis. The disease has characteristics of intrauterine growth retardation, metabolic decompensation with recurrent vomiting, persistent severe lactic acidosis, encep

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hépatoencéphalopathie par déficit combiné de la phosphorylation oxydative de type 1

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congenital metabolic disease | inborn metabolic disease

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maladie métabolique congénitale

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Applied Physiology, Nutrition, and Metabolism [ Canadian Journal of Applied Physiology | Canadian Journal of Sport Sciences ]

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Physiologie appliquée, nutrition et métabolisme [ Revue canadienne de physiologie appliquée | Revue canadienne des sciences du sport | Journal canadien des sciences du sport ]

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Anderen hebben gezocht naar : applied physiology nutrition and metabolism canadian journal of applied physiology canadian journal of sport sciences late metabolic acidosis of newborn metabolic acidosis chronic acidosis congenital metabolic disease inborn metabolic disease sub-acute ruminal acidosis sub-clinical acidosis

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Date index: 2021-06-12