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170 results
  1. ... disorder. Learn more about the gene associated with Carnitine-acylcarnitine translocase deficiency SLC25A20 Inheritance This condition is ... condition. Other Names for This Condition CACT deficiency Carnitine acylcarnitine translocase deficiency Carnitine-acylcarnitine carrier deficiency Additional ...
  2. ... disorder. Learn more about the gene associated with Carnitine palmitoyltransferase II deficiency CPT2 Inheritance This condition is ...
  3. ... disorder. Learn more about the gene associated with Carnitine palmitoyltransferase I deficiency CPT1A Inheritance This condition is ...
  4. ... Learn more about the gene associated with Primary carnitine deficiency SLC22A5 Inheritance This condition is inherited in ...
  5. ... epoetin between the two groups 261 . (Level 1+) Carnitine Haemodialysis patients No differences were observed in any ... 13. Supplements of vitamin C, folic acid or carnitine should not be prescribed as adjuvants specifically for ...
  6. ... Download PDF (351K) N.4.2. Acetyl-L-carnitine versus placebo for attention deficit hyperactivity disorder Download PDF (419K) N.4.3. Acetyl-L-carnitine versus placebo for dementia Download PDF (406K) N. ...
  7. ... other tissues. Health Conditions Related to Genetic Changes Carnitine palmitoyltransferase I deficiency More than 20 mutations in the CPT1A gene have been found to cause carnitine palmitoyltransferase I (CPT I) deficiency. Most of these ...
  8. ... other tissues. Health Conditions Related to Genetic Changes Carnitine palmitoyltransferase II deficiency More than 70 mutations in the CPT2 gene have been found to cause carnitine palmitoyltransferase II (CPT II) deficiency. These mutations lead ...
  9. ... muscles. Health Conditions Related to Genetic Changes Primary carnitine deficiency Many variants (also called mutations) in the SLC22A5 gene have been found to cause primary carnitine deficiency. Some of these variants create a premature ...
  10. ... other tissues. Health Conditions Related to Genetic Changes Carnitine-acylcarnitine translocase deficiency At least 27 mutations in the SLC25A20 gene have been found to cause carnitine-acylcarnitine translocase (CACT) deficiency. Although these mutations change ...
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