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Results 31 - 40 of 42 for AMMONIA OR BENZALKONIUM OR LIDOCAINE OR ASPIRIN
  1. UPB1 gene 
    ... down N-carbamyl-beta-alanine to beta-alanine, ammonia, and carbon dioxide. Both beta-aminoisobutyric acid and ...
    https://medlineplus.gov/genetics/gene/upb1 - Genetics
  2. OAT gene 
    ... which processes excess nitrogen (in the form of ammonia) that is generated when protein is broken down ...
    https://medlineplus.gov/genetics/gene/oat - Genetics
  3. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. The exact incidence of ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  4. Medium-chain acyl-CoA dehydrogenase deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. In the United States, ...
    https://medlineplus.gov/...m-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  5. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. The incidence of LCHAD ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  6. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... about half of individuals have an accumulation of ammonia in the blood. Buildup of these substances can ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  7. Mitochondrial trifunctional protein deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. Mitochondrial trifunctional protein deficiency ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  8. Short-chain acyl-CoA dehydrogenase deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections.In some people with ...
    https://medlineplus.gov/...t-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  9. Beta-ureidopropionase deficiency 
    ... down N-carbamyl-beta-alanine to beta-alanine, ammonia, and carbon dioxide. Both beta-aminoisobutyric acid and ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
  10. Dihydrolipoamide dehydrogenase deficiency 
    ... cardiomyopathy). Other features of this condition include excess ammonia in the blood (hyperammonemia), a buildup of molecules ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
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