pyridoxal phosphate has been researched along with Glycogen Storage Disease in 1 studies
Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).
pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal.
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pyridoxal phosphate is a covalently bound cofactor of glycogen phosphorylase." | 1.27 | Low muscle levels of pyridoxine in McArdle's syndrome. ( Cook, JD; Dempsey, WB; Feit, H; Haller, RG; Knochel, JP, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haller, RG | 1 |
| Dempsey, WB | 1 |
| Feit, H | 1 |
| Cook, JD | 1 |
| Knochel, JP | 1 |
1 other study available for pyridoxal phosphate and Glycogen Storage Disease
| Article | Year |
|---|---|
Low muscle levels of pyridoxine in McArdle's syndrome.
Topics: Adolescent; Adult; Animals; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Human | 1983 |