pyridoxal phosphate has been researched along with Mitochondrial Diseases 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.
Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
| Excerpt | Relevance | Reference |
|---|---|---|
| "At 3 years old, astatic myoclonic epilepsy appeared, with no response to levetiracetam." | 1.43 | Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient. ( García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O, 2016) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tort, F | 1 |
| Ugarteburu, O | 1 |
| Torres, MA | 1 |
| García-Villoria, J | 1 |
| Girós, M | 1 |
| Ruiz, A | 1 |
| Ribes, A | 1 |
1 other study available for pyridoxal phosphate and Mitochondrial Diseases
| Article | Year |
|---|---|
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine | 2016 |