- ... 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 ...
- ... of life 12.1.5.1.4. 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 ...
- ... 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 ...
- ... 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 ...
- ... vs placebo – all cause mortality Figure 180. Ornithine alpha-ketoglutarate vs placebo – time to complete healing Figure 181. Ornithine alpha-ketoglutarate vs placebo – mean% reduction in ulcer size Figure ...
- ... a novel enzymatic activity that promotes conversion of alpha-ketoglutarate to 2-hydroxyglutarate.[ 363 , 364 ] This novel activity ... IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate. Cancer Cell 17 (3): 225- ...
- ... 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. [ ...
- ... 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- ...
- ... 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, ...
- ... recessive disorder acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate (ARLIAK) (OMIM 618384 ), caused by biallelic pathogenic variants ...
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