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  2. Pyruvic acid - Wikipedia

    en.wikipedia.org/wiki/Pyruvic_acid

    Pyruvic acid (CH 3 COCOOH) is the simplest of the alpha-keto acids, with a carboxylic acid and a ketone functional group. Pyruvate , the conjugate base , CH 3 COCOO − , is an intermediate in several metabolic pathways throughout the cell.

  3. Urinalysis - Wikipedia

    en.wikipedia.org/wiki/Urinalysis

    Urine urobilinogen is increased in liver disease and hemolytic jaundice (jaundice due to increased destruction of red blood cells); in the latter case, urine bilirubin is typically negative. In bile duct obstruction, urine bilirubin increases but urobilinogen is normal or decreased, as bilirubin cannot reach the intestines to be converted to ...

  4. Alanine transaminase - Wikipedia

    en.wikipedia.org/wiki/Alanine_transaminase

    Alanine transaminase (ALT), also known as alanine aminotransferase (ALT or ALAT), formerly serum glutamate-pyruvate transaminase (GPT) or serum glutamic-pyruvic transaminase (SGPT), is a transaminase enzyme (EC 2.6.1.2) that was first characterized in the mid-1950s by Arthur Karmen and colleagues. [1]

  5. Urine test - Wikipedia

    en.wikipedia.org/wiki/Urine_test

    A urine test is any medical test performed on a urine specimen. The analysis of urine is a valuable diagnostic tool because its composition reflects the functioning of many body systems, particularly the kidneys and urinary system , and specimens are easy to obtain. [ 1 ]

  6. Reference ranges for urine tests - Wikipedia

    en.wikipedia.org/wiki/Reference_ranges_for_urine...

    Reference ranges for urine tests are described below: Measurement Lower limit Upper limit ... Red blood cells (RBCs) 0 [4] [2] 2 [2] - 3 [4] per High Power Field (HPF ...

  7. Pyruvate dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase...

    Pyruvate dehydrogenase deficiency (also known as pyruvate dehydrogenase complex deficiency or PDCD or PDH deficiency) is a rare neurodegenerative disorder associated with abnormal mitochondrial metabolism. PDCD is a genetic disease resulting from mutations in one of the components of the pyruvate dehydrogenase complex (PDC). [1]

  8. Maple syrup urine disease - Wikipedia

    en.wikipedia.org/wiki/Maple_syrup_urine_disease

    Maple syrup urine disease can be classified by its pattern of signs and symptoms or by its genetic cause. The most common and severe form of this disease is the classic type, which appears soon after birth, and as long as it remains untreated, gives rise to progressive and unremitting symptoms.

  9. Urine electrolyte levels - Wikipedia

    en.wikipedia.org/wiki/Urine_electrolyte_levels

    Urine electrolyte levels can be measured in a medical laboratory for diagnostic purposes. The urine concentrations of sodium , chlorine and potassium may be used to investigate conditions such as abnormal blood electrolyte levels, acute kidney injury , metabolic alkalosis and hypovolemia .