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The Journal of Pediatrics, 1981
PRIMARY LACTIC ACIDOSIS/LACTIC ACIDURIA occurs in patients with a deficiency of specific enzymes involved in the metabolism of pyruvate, such as pyruvate carboxylase, pyruvate dehydrogenase, and phosphoenolpyruvate carboxykinase, and in other metabolic disorders such as type 1 glycogen storage disease, hereditary fructose intolerance, and disorders of ...
J G, Rogers +3 more
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PRIMARY LACTIC ACIDOSIS/LACTIC ACIDURIA occurs in patients with a deficiency of specific enzymes involved in the metabolism of pyruvate, such as pyruvate carboxylase, pyruvate dehydrogenase, and phosphoenolpyruvate carboxykinase, and in other metabolic disorders such as type 1 glycogen storage disease, hereditary fructose intolerance, and disorders of ...
J G, Rogers +3 more
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Endocrinology and Metabolism Clinics of North America, 1993
Lactic acidosis is the most common metabolic acidosis. At clinical presentation, several causes usually can be identified. The liver is a major site of removal of lactate and hydrogen ions, and abnormalities in the aerobic metabolism of lactate by mitochondria in hepatocytes and other cells may contribute to many clinical conditions in which ...
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Lactic acidosis is the most common metabolic acidosis. At clinical presentation, several causes usually can be identified. The liver is a major site of removal of lactate and hydrogen ions, and abnormalities in the aerobic metabolism of lactate by mitochondria in hepatocytes and other cells may contribute to many clinical conditions in which ...
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Disease-a-Month, 1989
An understanding of the pathophysiology of lactic acidosis is crucial in facilitating the optimal care of critically ill patients. The relevant biochemistry of lactic acidosis is reviewed, and the more controversial aspects relating to the genesis of the acidosis are highlighted.
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An understanding of the pathophysiology of lactic acidosis is crucial in facilitating the optimal care of critically ill patients. The relevant biochemistry of lactic acidosis is reviewed, and the more controversial aspects relating to the genesis of the acidosis are highlighted.
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Annals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1989
About ten years ago, Zilva' argued that there is a fundamental difference between hydrolysis of adenosine triphosphate (ATP) under aerobic and anaerobic conditions: 'H+ produced by hydrolysis of ATp4yielded by anaerobic glycolysis is only significant because it is not used in resynthesis' (of ATP presumably).
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About ten years ago, Zilva' argued that there is a fundamental difference between hydrolysis of adenosine triphosphate (ATP) under aerobic and anaerobic conditions: 'H+ produced by hydrolysis of ATp4yielded by anaerobic glycolysis is only significant because it is not used in resynthesis' (of ATP presumably).
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Annals of Internal Medicine, 1970
Excerpt To the editor: A case of lactic acidosis is described in the September issue (OLIVAPP, SCHWARTZHA: Survival of a patient with spontaneous lactic acidosis).
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Excerpt To the editor: A case of lactic acidosis is described in the September issue (OLIVAPP, SCHWARTZHA: Survival of a patient with spontaneous lactic acidosis).
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Nutrition in Clinical Practice, 2005
d‐Lactic acidosis, also referred to as d‐lactate encephalopathy, is a rare neurologic syndrome that occurs in individuals with short bowel syndrome or following jejuno‐ileal bypass surgery. Symptoms typically present after the ingestion of high‐carbohydrate feedings.
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d‐Lactic acidosis, also referred to as d‐lactate encephalopathy, is a rare neurologic syndrome that occurs in individuals with short bowel syndrome or following jejuno‐ileal bypass surgery. Symptoms typically present after the ingestion of high‐carbohydrate feedings.
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Acid-Base Disorders, 2008