lactic acid has been researched along with Brain Diseases, Metabolic, Familial in 12 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 |
|---|---|---|
| "Her symptoms consisted of a few convulsions between 2." | 1.33 | [Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age]. ( Garcia-Segura, JM; Merinero, B; Pascual-Castroviejo, I; Pascual-Pascual, SI; Ugarte, M; Velazquez, R; Viaño, J, 2005) |
| "Mitochondrial diseases are a group of inherited disorders caused by a derangement of mitochondrial respiration." | 1.32 | Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease. ( Barker, PB; Crawford, TO; Lin, DD, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (50.00) | 29.6817 |
| 2010's | 6 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boyer, M | 1 |
| Sowa, M | 1 |
| Di Meo, I | 1 |
| Eftekharian, S | 1 |
| Steenari, MR | 1 |
| Tiranti, V | 1 |
| Abdenur, JE | 1 |
| Sahebekhtiari, N | 1 |
| Fernandez-Guerra, P | 1 |
| Nochi, Z | 1 |
| Carlsen, J | 1 |
| Bross, P | 1 |
| Palmfeldt, J | 1 |
| Toplak, M | 1 |
| Brunner, J | 1 |
| Schmidt, J | 1 |
| Macheroux, P | 1 |
| Anttonen, AK | 1 |
| Hilander, T | 1 |
| Linnankivi, T | 1 |
| Isohanni, P | 1 |
| French, RL | 1 |
| Liu, Y | 1 |
| Simonović, M | 1 |
| Söll, D | 1 |
| Somer, M | 1 |
| Muth-Pawlak, D | 1 |
| Corthals, GL | 1 |
| Laari, A | 1 |
| Ylikallio, E | 1 |
| Lähde, M | 1 |
| Valanne, L | 1 |
| Lönnqvist, T | 1 |
| Pihko, H | 1 |
| Paetau, A | 1 |
| Lehesjoki, AE | 1 |
| Suomalainen, A | 1 |
| Tyynismaa, H | 1 |
| Aguiar, AS | 1 |
| Tuon, T | 1 |
| Albuquerque, MM | 1 |
| Rocha, GS | 1 |
| Speck, AE | 1 |
| Araújo, JC | 1 |
| Dafré, AL | 1 |
| Prediger, RD | 1 |
| Pinho, RA | 1 |
| Girard, N | 1 |
| Jain-Ghai, S | 1 |
| Cameron, JM | 1 |
| Al Maawali, A | 1 |
| Blaser, S | 1 |
| MacKay, N | 1 |
| Robinson, B | 1 |
| Raiman, J | 1 |
| Lin, DD | 1 |
| Crawford, TO | 1 |
| Barker, PB | 1 |
| Pascual-Castroviejo, I | 1 |
| Pascual-Pascual, SI | 1 |
| Merinero, B | 1 |
| Ugarte, M | 1 |
| Garcia-Segura, JM | 1 |
| Viaño, J | 1 |
| Velazquez, R | 1 |
| José da Rocha, A | 1 |
| Túlio Braga, F | 1 |
| Carlos Martins Maia, A | 1 |
| Jorge da Silva, C | 1 |
| Toyama, C | 1 |
| Pereira Pinto Gama, H | 1 |
| Kok, F | 1 |
| Rodrigues Gomes, H | 1 |
| Benardis, PG | 1 |
| Ikomi, AA | 1 |
| Bateman, SG | 1 |
| Bowyer, JJ | 1 |
| Pearl, PL | 1 |
| Krasnewich, D | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| In Vivo Investigation on Mitochondrial Dysfunction in Post-COVID Fatigue and Cancer Fatigue.[NCT05753228] | 90 participants (Anticipated) | Interventional | 2022-12-09 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for lactic acid and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
[Magnetic resonance spectroscopy for cerebral imaging].
Topics: Apoptosis; Aspartic Acid; Asphyxia Neonatorum; Biomarkers, Tumor; Brain; Brain Diseases; Brain Disea | 2010 |
Complex II deficiency--a case report and review of the literature.
Topics: Brain Diseases, Metabolic, Inborn; Electron Transport Complex II; Fatal Outcome; Female; Humans; Inf | 2013 |
Lactate detection by MRS in mitochondrial encephalopathy: optimization of technical parameters.
Topics: Brain Diseases, Metabolic, Inborn; Humans; Lactic Acid; Magnetic Resonance Spectroscopy; Mitochondri | 2008 |
9 other studies available for lactic acid and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Response to medical and a novel dietary treatment in newborn screen identified patients with ethylmalonic encephalopathy.
Topics: Acetylcysteine; Amino Acids; Biomarkers; Brain Diseases, Metabolic, Inborn; Cysteine; Diet; Female; | 2018 |
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria.
Topics: Brain Diseases, Metabolic, Inborn; Cell Adhesion; Cell Cycle; Down-Regulation; Endoplasmic Reticulum | 2019 |
Biochemical characterization of human D-2-hydroxyglutarate dehydrogenase and two disease related variants reveals the molecular cause of D-2-hydroxyglutaric aciduria.
Topics: Alcohol Oxidoreductases; Amino Acid Substitution; Brain Diseases, Metabolic, Inborn; Catalysis; Elec | 2019 |
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.
Topics: Adolescent; Amino Acyl-tRNA Synthetases; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Pre | 2015 |
The exercise redox paradigm in the Down's syndrome: improvements in motor function and increases in blood oxidative status in young adults.
Topics: Adult; Antioxidants; Biomarkers; Brain; Brain Diseases, Metabolic, Inborn; Catalase; Down Syndrome; | 2008 |
Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.
Topics: Adolescent; Adult; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Female; Fourie | 2003 |
[Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age].
Topics: Basal Ganglia; Brain; Brain Chemistry; Brain Diseases, Metabolic, Inborn; Carnitine; Cells, Cultured | 2005 |
An inborn error of metabolism imitating hypoxic-ischaemic encephalopathy.
Topics: Adult; Brain Diseases, Metabolic, Inborn; Diagnosis, Differential; Fatal Outcome; Female; Fetal Hypo | 2000 |
Neurologic course of congenital disorders of glycosylation.
Topics: Aspartic Acid; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Congenital Disorde | 2001 |