Results 1 - 10 of 56 for "L-Carnitine"
  1. Primary carnitine deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). Carnitine, a natural substance acquired mostly through the diet, ...
  2. Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 2. This enzyme is essential for fatty ...
  3. Carnitine palmitoyltransferase I (CPT I) deficiency is a condition that prevents the body from using certain fats ... liver (hepatomegaly), liver malfunction, and elevated levels of carnitine in the blood. Carnitine, a natural substance acquired ...
  4. Carnitine-acylcarnitine translocase (CACT) deficiency is a condition that prevents the body from using certain fats for ... gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT). This protein is essential for ...
  5. ... gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT). This protein is essential for ... must be attached to a substance known as carnitine to enter mitochondria. Once these fatty acids are ...
  6. ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 1A, which is found in the liver. ... they are attached to a substance known as carnitine. Carnitine palmitoyltransferase 1A connects carnitine to long-chain ...
  7. ... membrane, where it transports a substance known as carnitine into the cell. Carnitine is mainly obtained from the diet and is ... SLC22A5 gene have been found to cause primary carnitine deficiency. Some of these mutations create a premature ...
  8. ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 2. This enzyme is essential for fatty ... must be attached to a substance known as carnitine to enter mitochondria. Once these fatty acids are ...
  9. Metabolic Diseases of Muscle (Muscular Dystrophy Association) - PDF  
    ... acid maltase deficiency; debrancher enzyme deficiency; Tarui disease; carnitine deficiency; carnitine palmityl transferase deficiency; Cori disease; Forbes ...
  10. Mitochondrial Myopathies (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscular Dystrophy Association ... PDF ... mitonchondrial ...
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