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21 results
  1. Disorders of Intracellular Cobalamin Metabolism - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1328
    ... in which methionine level is elevated (see Differential Diagnosis , Cystathionine beta-synthase deficiency ). Other findings that can be seen on PAA analysis: Hyperhomocysteinemia and mixed disulfides (which are also excreted in ...
  2. Isolated Methylmalonic Acidemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1231
    ... acidemia/aciduria and hyperhomocysteinemia/homocystinuria) and cblD -homocystinuria ... genetic causes of elevated methylmalonic acidemia/aciduria ...
  3. MTRR gene 
    https://medlineplus.gov/genetics/gene/mtrr
    ... reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families. J Inherit Metab Dis. 2002 ...
  4. Hypermethioninemia 
    https://medlineplus.gov/genetics/condition/hypermethioninemia
    ... RH, Wagner C, Borschel MW. Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap. ...
  5. Excluded studies - Parkinson’s disease in adults: diagnosis and management - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK535861
    ... E., 20060719, Vitamins and entacapone in levodopa-induced hyperhomocysteinemia: a randomized controlled study, Neurology, 66, 1941–1943, ... the protective effect of vitamins on levodopa induced hyperhomocysteinemia Saint-Hilaire, M., Carbohydrate-protein ratio of 7: ...
  6. Results of Systematic Review of Research on Diagnosis and Treatment of Coronary Heart Disease in Women: Summary - AHRQ .... 
    https://www.ncbi.nlm.nih.gov/books/NBK11919
    ... or good evidence suggests that hyperlipidemia, diabetes and hyperhomocysteinemia are risk factors for CHD in women. Only ... 80, Results of Systematic Review of Research on Diagnosis and Treatment of Coronary Heart Disease in Women ( ...
  7. Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1524
    ... R, Shih VE. Stroke in young patients with hyperhomocysteinemia due to cystathionine β-synthase deficiency. Neurology. 2003; ...
  8. Nonketotic Hyperglycinemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1357
    ... seizures ↑ plasma & CSF glycine levels Combined methylmalonic aciduria & hyperhomocysteinemia Glycine transport defect GLYT1 encephalopathy SLC6A9 AR Neonatal ...
  9. Hereditary Folate Malabsorption - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1673
    ... Methylenetetrahydrofolate dehydrogenase 1 deficiency (combined immunodeficiency & megaloblastic anemia ± hyperhomocysteinemia) (OMIM 617780 ) AR Early onset, megaloblastic anemia, hemolytic ...
  10. Factor V Leiden Thrombophilia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1368
    ... the use of vitamin supplementation in individuals with hyperhomocysteinemia and a history of VTE MTHFR variants, as ...
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