folic acid has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 6 studies
| 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 | 6 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alonzo, JR; Field, MS; Stover, PJ; Venkataraman, C | 1 |
| Benoist, JF; Lubetzki, C; Masingue, M; Moussa, F; Nadjar, Y; Roze, E; Sedel, F | 1 |
| Schnellmann, RG; Stallons, LJ; Whitaker, RM | 1 |
| Cauli, O; González-Guevara, L; Guevara-Campos, J | 1 |
| Artuch, R; Aylett, SB; Casado, M; Hargreaves, I; Heales, S; Molero-Luis, M; Montoya, J; Ormazabal, A; Rahman, S | 1 |
| Quadros, EV; Ramaekers, V; Sequeira, JM | 1 |
2 review(s) available for folic acid and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Can folic acid have a role in mitochondrial disorders?
Topics: Animals; Biological Transport; DNA, Mitochondrial; Folic Acid; Folic Acid Deficiency; Humans; Leucovorin; Mitochondria; Mitochondrial Diseases | 2015 |
Clinical recognition and aspects of the cerebral folate deficiency syndromes.
Topics: Autoantibodies; Folate Receptor 1; Folic Acid; Folic Acid Deficiency; Humans; Leucovorin; Mitochondrial Diseases; Mutation | 2013 |
4 other study(ies) available for folic acid and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
The mitochondrial inner membrane protein MPV17 prevents uracil accumulation in mitochondrial DNA.
Topics: Biological Transport, Active; DNA, Mitochondrial; Folic Acid; Gene Expression Regulation; HeLa Cells; Humans; Membrane Proteins; Mitochondrial Diseases; Mitochondrial Proteins; Thymidine Monophosphate; Uracil | 2018 |
Cerebral folate deficiency in adults: A heterogeneous potentially treatable condition.
Topics: Adolescent; Adult; Aged; Calcinosis; Cerebellar Diseases; Child; Child, Preschool; Female; Folic Acid; Folic Acid Deficiency; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intellectual Disability; Magnetic Resonance Imaging; Male; Middle Aged; Mitochondrial Diseases; Mutation; Proteins; Retrospective Studies; Tetrahydrofolates; White Matter; Young Adult | 2019 |
Suppressed mitochondrial biogenesis in folic acid-induced acute kidney injury and early fibrosis.
Topics: Actins; Acute Kidney Injury; Animals; Blotting, Western; Collagen; Creatinine; DNA; Electron Transport Complex IV; Fibrosis; Folic Acid; Glycosuria; Hematinics; Homeostasis; Male; Mice; Mitochondria; Mitochondrial Diseases; RNA, Messenger | 2014 |
Autism and intellectual disability associated with mitochondrial disease and hyperlactacidemia.
Topics: Carnitine; Child Development Disorders, Pervasive; Child, Preschool; Female; Folic Acid; Humans; Hyperlactatemia; Infant; Intellectual Disability; Male; Mitochondrial Diseases; Ubiquinone; Vitamins | 2015 |