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  1. Riboflavin Transporter Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK299312
    ... Search term GeneReviews Advanced Search Help < Prev Next > Riboflavin Transporter Deficiency Elisa Cali , MD, Natalia Dominik , BSc, ... responsive to riboflavin supplementation [ Kang et al 2020 ]. Riboflavin Deficiency 2 and 3 While most individuals with ...
  2. Riboflavin transporter deficiency neuronopathy: MedlinePlus Genetics 
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy
    ... neuronopathy. Learn more about the genes associated with Riboflavin transporter deficiency neuronopathy SLC52A2 SLC52A3 Inheritance Riboflavin transporter ...
  3. Riboflavin 
    https://medlineplus.gov/ency/article/002411.htm
    Riboflavin is a type of B vitamin. It is water soluble, which means it is not stored ... Riboflavin (vitamin B2) works with the other B vitamins. It is important for body growth. It helps ...
  4. Riboflavin 
    https://ods.od.nih.gov/factsheets/Riboflavin-Consumer
    https://ods.od.nih.gov/factsheets/Riboflavin-Consumer/ ... https://ods.od.nih.gov/factsheets/Riboflavin-Consumer/ ... https://ods.od.nih.gov/factsheets/Riboflavin-Consumer/
  5. B Vitamins 
    https://medlineplus.gov/bvitamins.html
    The B vitamins are: B1 (thiamine) B2 (riboflavin) B3 (niacin) B5 (pantothenic acid) B6 B7 (biotin) B12 Folic acid These vitamins help the process your body uses to get or make ...
  6. Multiple Acyl-CoA Dehydrogenase Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK558236
    ... ETFA , ETFB , or ETFDH. Differential Diagnosis Disorders of Riboflavin Metabolism Disorders of riboflavin metabolism can mimic multiple acyl-CoA dehydrogenase deficiency ( ...
  7. SLC52A2 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/slc52a2
    ... and proteins. Health Conditions Related to Genetic Changes Riboflavin transporter deficiency neuronopathy At least 11 mutations in the SLC52A2 gene have been found to cause riboflavin transporter deficiency neuronopathy. This neurological condition encompasses two ...
  8. SLC52A3 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/slc52a3
    ... and proteins. Health Conditions Related to Genetic Changes Riboflavin transporter deficiency neuronopathy More than two dozen mutations ... the SLC52A3 gene have been found to cause riboflavin transporter deficiency neuronopathy. This neurological condition encompasses two ...
  9. PNPO Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK581452
    ... cofactor function of PLP and folinic acid derivatives. Riboflavin. Individuals with PNPO variants affecting the flavin mononucleotide ... supplementation with 100-200 mg/day of oral riboflavin. See Genotype-Phenotype Correlations . Other. Absence of seizures ...
  10. NLM Digital Collections - Free Radical Formation in Riboflavin Complexes 
    Publication: National Academy of Sciences (U.S.), 15 September 1958
    resource.nlm.nih.gov/101584924X120
    Free Radical Formation in Riboflavin Complexes ... Riboflavin ... complexes formed by proteins and substances such as riboflavin (vitamin B-2). ... Free Radical Formation in Riboflavin Complexes Free Radicals Riboflavin In ... Isenberg explored how free radicals--molecules with an unpaired electron-- ...
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