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Displaying results 11 - 14 of 14 in total
  1. Pathway

    Leigh Syndrome

    smpdb.ca/view/SMP0125770
    Disease

    Leigh Syndrome, also called Leigh Disease or infantile subacute necrotizing encephalopathy, is a rare inborn error of metabolism (IEM) and autosomal recessive disorder that is caused by a mutation of any one of 75 different genes. Disrup...

    Drugs: Pyruvic acid · Biotin · Adenosine phosphate · Glutathione · NADH · ATP +13 more
  2. Pathway

    Primary Hyperoxaluria II, PH2

    smpdb.ca/view/SMP0125773
    Disease

    Primary hyperolaria type 2 (PH2) is a rare condition resulting from glyoxylate reductase/hydroxypyruvate reductase (GR/HPR) enzyme deficiency. PH2 results in calcium oxalate (also known as oxalic acid) deposits and end-stage renal diseas...

    Drugs: Pyruvic acid · Biotin · Adenosine phosphate · Glutathione · NADH · ATP +13 more
  3. Pathway

    Fosphenytoin (Antiarrhythmic) Action Pathway

    smpdb.ca/view/SMP0000326
    Drug action

    Parenteral phenytoin sodium was originally prepared in 40% propylene glycol and 10% ethanol at pH 12.

    Drugs: ATP · Phenytoin · Fosphenytoin · Potassium cation · Calcium
  4. Pathway

    Fosphenytoin (Antiarrhythmic) Metabolism Pathway

    smpdb.ca/view/SMP0000618
    Drug metabolism

    Parenteral phenytoin sodium was originally prepared in 40% propylene glycol and 10% ethanol at pH 12.

    Drugs: Phenytoin · Fosphenytoin