pyridoxine has been researched along with Autosomal Chromosome Disorders in 6 studies
4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol: structure in first source
vitamin B6 : Any member of the group of pyridines that exhibit biological activity against vitamin B6 deficiency. Vitamin B6 deficiency is associated with microcytic anemia, electroencephalographic abnormalities, dermatitis with cheilosis (scaling on the lips and cracks at the corners of the mouth) and glossitis (swollen tongue), depression and confusion, and weakened immune function. Vitamin B6 consists of the vitamers pyridoxine, pyridoxal, and pyridoxamine and their respective 5'-phosphate esters (and includes their corresponding ionized and salt forms).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pyridoxine-dependent seizure (PDS) is a rare autosomal recessive intractable seizure disorder only controlled by a daily supplementation of pharmacological doses of pyridoxine (Vitamin B6)." | 5.33 | Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures. ( Bennett, CL; Chance, PF; Glass, IA; Gospe, SM; Huynh, HM, 2005) |
| "Pyridoxine-dependent seizure (PDS) is a rare autosomal recessive intractable seizure disorder only controlled by a daily supplementation of pharmacological doses of pyridoxine (Vitamin B6)." | 1.33 | Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures. ( Bennett, CL; Chance, PF; Glass, IA; Gospe, SM; Huynh, HM, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (83.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bennett, CL | 1 |
| Huynh, HM | 1 |
| Chance, PF | 1 |
| Glass, IA | 1 |
| Gospe, SM | 1 |
| Vacarezza, R | 1 |
| Papayannis, AG | 1 |
| Stathakis, NE | 1 |
| Kyrkoy, K | 1 |
| Panani, A | 1 |
| Gardikas, C | 1 |
| Gamstorp, I | 1 |
| Broyer, M | 1 |
| Berger, R | 1 |
| Tada, K | 1 |
| Yoshida, T | 1 |
| Yokoyama, Y | 1 |
| Sato, T | 1 |
| Nakagawa, H | 1 |
1 review available for pyridoxine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
[Preleukemic states].
Topics: Adrenal Cortex Hormones; Aged; Alkaline Phosphatase; Androgens; Antineoplastic Agents; Blood Cell Co | 1982 |
5 other studies available for pyridoxine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures.
Topics: Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 5; Female; Genes, Recessive; Gene | 2005 |
Primary acquired sideroblastic anaemia associated with chronic lymphocytic leukaemia.
Topics: Aged; Anemia, Sideroblastic; Biopsy; Blood Cells; Blood Protein Electrophoresis; Bone Marrow; Bone M | 1974 |
[Vitamin B6-dependency syndrome].
Topics: Asphyxia Neonatorum; Chromosome Aberrations; Chromosome Disorders; Female; Humans; Infant, Newborn; | 1974 |
[Cystathioninuria].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Chromosome Aberrations; Chromosom | 1969 |
Cystathioninuria not associated with vitamin B6 dependency: a probably new type of cystathioninuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Child; Child, Pres | 1968 |