pyridoxine has been researched along with 5-methyltetrahydrofolate in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hyland, K; Surtees, R | 1 |
| Chadefaux-Vekemans, B; Drüeke, T; Jungers, P; Massy, ZA; Touam, M; Zingraff, J | 1 |
| Al-Baradie, RS; Chaudhary, MW | 1 |
| Carrasco-Marina, ML; Castro-Reguera, M; Garcia-Ezquiaga, J; Gutierrez-Cruz, N; Iglesias-Escalera, G; Perez-Gonzalez, B | 1 |
1 trial(s) available for pyridoxine and 5-methyltetrahydrofolate
| Article | Year |
|---|---|
Effective correction of hyperhomocysteinemia in hemodialysis patients by intravenous folinic acid and pyridoxine therapy.
Topics: Adult; Aged; Erythrocytes; Female; Humans; Hyperhomocysteinemia; Injections, Intravenous; Kidney Failure, Chronic; Leucovorin; Male; Middle Aged; Pyridoxine; Renal Dialysis; Tetrahydrofolates; Vitamin B 12 | 1999 |
3 other study(ies) available for pyridoxine and 5-methyltetrahydrofolate
| Article | Year |
|---|---|
L-3,4-dihydroxyphenylalanine (levodopa) lowers central nervous system S-adenosylmethionine concentrations in humans.
Topics: Adolescent; Akinetic Mutism; Biopterins; Child, Preschool; Humans; Infant; Levodopa; Methionine; NADH, NADPH Oxidoreductases; Phenylketonurias; Pyridoxine; S-Adenosylmethionine; Tetrahydrofolates; Tyrosine | 1990 |
Diagnosis and management of cerebral folate deficiency. A form of folinic acid-responsive seizures.
Topics: Atrophy; Brain; Brain Diseases, Metabolic, Inborn; Child Development Disorders, Pervasive; Child, Preschool; Consanguinity; Developmental Disabilities; Early Diagnosis; Electroencephalography; Epilepsies, Myoclonic; Female; Folate Receptor 1; Folic Acid Deficiency; Humans; Leucovorin; Magnetic Resonance Imaging; Male; Mutation, Missense; Point Mutation; Pyridoxine; Siblings; Tetrahydrofolates | 2014 |
[Pyridoxine-dependent epilepsy due to deficiency in the PNPO gene].
Topics: Adolescent; Brain Diseases, Metabolic; Chromosomes, Human, Pair 17; Epilepsy; Female; Humans; Hypoxia-Ischemia, Brain; Mutation, Missense; Polymorphism, Single Nucleotide; Pyridoxaminephosphate Oxidase; Pyridoxine; Seizures; Tetrahydrofolates; Uniparental Disomy | 2019 |