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10 results
  1. ... Lerebours E, Kern J, et al. Efficacy and safety of ornithine alpha-ketoglutarate in heel pressure ulcers in elderly patients: results ...
  2. ... of life 5.2.5.1.11. Ornithine alpha-ketoglutarate versus placebo One study (n=160) showed there is potentially no clinical difference between ornithine alpha-ketoglutarate and placebo for rate of complete healing of ...
  3. ... a finding in other genetically defined microcephaly syndromes. Alpha-ketoglutarate. Among other genetic malformation syndromes, a similar level ... DLD Dihydrolipoamide dehydrogenase deficiency AR ↑ levels of urinary alpha-ketoglutarate may be seen in persons w/pathogenic variants ...
  4. ... or third month of life. A compound called alpha-ketoglutaric acid can be detected in their urine (alpha-ketoglutaric ... disease</synonym><synonym >Familial hyperlysinemia</synonym><synonym ... disease</synonym><synonym >Saccharopine dehydrogenase deficiency ...
  5. ... a novel enzymatic activity that promotes conversion of alpha-ketoglutarate to 2-hydroxyglutarate.[ 187 , 188 ] This novel activity ... IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate. Cancer Cell 17 (3): 225- ...
  6. ... glycosylation defect Riley et al [2017] α-KGDH = alpha-ketoglutarate dehydrogenase; AR = autosomal recessive; BCAA = branched-chain amino ... Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. Orphanet J Rare Dis. 2013; 8 :192. [ ...
  7. ... of BCKD is shared with the pyruvate and alpha-ketoglutarate dehydrogenase complexes, and MSUD type 3 is characterized by increased urinary excretion of BCKAs and alpha-ketoglutarate accompanied by elevated plasma concentrations of lactate, pyruvate, ...
  8. ... GR, Tacconi C, Zoli G. Use of pyridoxine-alpha-ketoglutarate (PAK) in hepatic encephalopathy. International Journal of Clinical ... Garcia-Ramos G, Fernandez-Zertuche M. Efficacy and safety of L-ornithine-L-aspartate (LOLA) administration. Open ...
  9. ... Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. Orphanet J Rare Dis. 2013; 8 :192. [ ...
  10. ... methylcitrate as well as 3-methylcrotonylglycine, 3-hydroxybutyrate, alpha-ketoglutarate, & 3-hydroxyisovalerate. Plasma acylcarnitine profile in carbonic anhydrase ...