lactic acid has been researched along with Abnormalities, Congenital, Nervous System in 2 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
| 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) |
| "Although confirmation of PDH deficiency depends on specialized biochemical analyses, neonatal MRI plays a role in evaluating the pattern and extent of brain damage, and potentially in early diagnosis and clinical decision making." | 1.35 | Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings. ( Cruz, R; Leijser, LM; Magalhães, Z; Ribeiro, M; Rocha, JF; Soares-Fernandes, JP; Teixeira-Gomes, R, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 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 |
| Soares-Fernandes, JP | 1 |
| Teixeira-Gomes, R | 1 |
| Cruz, R | 1 |
| Ribeiro, M | 1 |
| Magalhães, Z | 1 |
| Rocha, JF | 1 |
| Leijser, LM | 1 |
2 other studies available for lactic acid and Abnormalities, Congenital, Nervous System
| 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 |
Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings.
Topics: Brain; Diagnosis, Differential; Diffusion Magnetic Resonance Imaging; Humans; Infant, Newborn; Lacti | 2008 |