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Results 1 - 10 of 40 for b vitamins
  1. Cerebral folate transport deficiency 
    ... that develops from a shortage (deficiency) of the B-vitamin folate (also called vitamin B9) in the brain. ... where it attaches (binds) to folate, allowing the vitamin to be brought into the cell. Folate ... Citation on PubMed Perez-Duenas B, Ormazabal A, Toma C, Torrico B, Cormand B, ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  2. Hereditary folate malabsorption 
    ... with the body's ability to absorb certain B vitamins (called folates) from food. Folates are important for ... folates in their body because they obtain these vitamins from their mother's blood before ... on PubMed Lasry I, Berman B, Straussberg R, Sofer Y, Bessler H, Sharkia M, ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  3. Biotinidase deficiency 
    ... enzyme called biotinidase. This enzyme recycles biotin, a B vitamin found in foods such as liver, egg yolks, ... Epub 2010 Jan 11. Citation on PubMed Wolf B. The neurology of biotinidase deficiency. Mol ... Epub 2011 Jun 12. Citation on PubMed
    https://medlineplus.gov/genetics/condition/biotinidase-deficiency - Genetics
  4. Glutamate formiminotransferase deficiency 
    ... their urine, they have elevated amounts of certain B vitamins (called folates) in their blood.The severe form ... in producing one of several forms of the vitamin folate, which has many important functions in the body.FTCD gene mutations ... Fowler B. The folate cycle and disease in humans. Kidney ...
    https://medlineplus.gov/...glutamate-formiminotransferase-deficiency - Genetics
  5. Holocarboxylase synthetase deficiency 
    ... important for the effective use of biotin, a B vitamin found in foods such as liver, egg yolks, ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  6. Methylmalonic acidemia with homocystinuria 
    ... 1056/NEJMoa072200. Citation on PubMed Froese DS, Fowler B, Baumgartner MR. Vitamin B12 , folate, and the methionine remethylation cycle-biochemistry, ... LMBRD1: the gene for the cblF defect of vitamin B(1)(2) metabolism. J Inherit Metab Dis. 2011 ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  7. Imerslund-Gräsbeck syndrome 
    ... IGS1 PubMed Grasbeck R. Imerslund-Grasbeck syndrome (selective vitamin B(12) malabsorption with proteinuria). Orphanet J Rare Dis. ... anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15;96( ...
    https://medlineplus.gov/.../condition/imerslund-grasbeck-syndrome - Genetics
  8. Vitamin D-dependent rickets 
    ... Al-Rijjal RA, Bircan I, Akcurin S, Meyer B, Shi Y. Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A. Clin Endocrinol (Oxf). ...
    https://medlineplus.gov/.../condition/vitamin-d-dependent-rickets - Genetics
  9. Ataxia with vitamin E deficiency 
    ... D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S. Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  10. Intervertebral disc disease 
    ... Citation on PubMed Toktas ZO, Eksi MS, Yilmaz B, Demir MK, Ozgen S, Kilic T, Konya D. Association of collagen I, IX and vitamin D receptor gene polymorphisms with radiological severity of ...
    https://medlineplus.gov/.../condition/intervertebral-disc-disease - Genetics
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