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Results 1 - 10 of 18 for melas
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  1. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a condition that affects many of the ... loss of intellectual function (dementia).Most people with MELAS have a buildup of lactic acid in their ...
  2. ... UCN)) gene detected in a family with MERRF/MELAS overlap syndrome. Biochem Biophys Res Commun. 1995 Sep ...
  3. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). This condition affects many of the body's ... myopathy). The MT-ND5 gene variants that cause MELAS alter single nucleotides in the gene. Most people ...
  4. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). This condition is characterized by recurrent severe headaches, ... described above) is the most common mutation in MELAS. It is responsible for about 80 percent of ...
  5. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) have a mutation in the MT-TH gene. ... combination of signs and symptoms is called MERRF/MELAS overlap syndrome.MT-TH gene mutations that cause ...
  6. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). Some of these genes provide instructions for making ... more than 80 percent of all cases of MELAS. This mutation, written as A3243G, replaces the nucleotide ...
  7. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). These affected individuals are said to have MERRF/MELAS overlap syndrome. Additional signs and symptoms of this ...
  8. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). Most cases of MELAS are caused by mutations in other mitochondrial genes, ...
  9. ... mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). Most cases of MELAS are caused by mutations in other mitochondrial genes, ...
  10. ... a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype. Arch Neurol. 2004 Feb;61(2): ... UCN)) gene detected in a family with MERRF/MELAS overlap syndrome. Biochem Biophys Res Commun. 1995 Sep ...
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