pyridoxine has been researched along with Gangliosidoses in 2 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).
Gangliosidoses: A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 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 |
---|---|
Sakuraba, H | 1 |
Itoh, K | 1 |
Shimmoto, M | 1 |
Utsumi, K | 1 |
Kase, R | 1 |
Hashimoto, Y | 1 |
Ozawa, T | 1 |
Ohwada, Y | 1 |
Imataka, G | 1 |
Eguchi, M | 1 |
Furukawa, T | 1 |
Schepers, U | 1 |
Sandhoff, K | 1 |
Iinuma, K | 1 |
2 other studies available for pyridoxine and Gangliosidoses
Article | Year |
---|---|
GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patient.
Topics: Anticonvulsants; Blotting, Western; Cells, Cultured; Chromatography, Thin Layer; Electroencephalogra | 1999 |
[Convulsive disorders in inborn errors of metabolism (author's transl)].
Topics: Electroencephalography; Gangliosidoses; Homocystinuria; Humans; Metabolism, Inborn Errors; Phenylket | 1979 |