pyridoxine has been researched along with Glycogen Storage Disease in 4 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).
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pyridoxal phosphate is a covalently bound cofactor of glycogen phosphorylase." | 1.27 | Low muscle levels of pyridoxine in McArdle's syndrome. ( Cook, JD; Dempsey, WB; Feit, H; Haller, RG; Knochel, JP, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haller, RG | 1 |
| Dempsey, WB | 1 |
| Feit, H | 1 |
| Cook, JD | 1 |
| Knochel, JP | 1 |
| Snyderman, SE | 1 |
| Holtzman, NA | 1 |
| Panizon, F | 1 |
2 reviews available for pyridoxine and Glycogen Storage Disease
| Article | Year |
|---|---|
The dietary therapy of inherited metabolic disease.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C | 1975 |
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
2 other studies available for pyridoxine and Glycogen Storage Disease
| Article | Year |
|---|---|
Low muscle levels of pyridoxine in McArdle's syndrome.
Topics: Adolescent; Adult; Animals; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Human | 1983 |
[Diseases due to enzyme defects in childhood. Nosography and recent progress].
Topics: Amino Acid Metabolism, Inborn Errors; Coenzymes; Diet Therapy; Dietary Proteins; Glucose-6-Phosphata | 1971 |