pyridoxine has been researched along with Nephritis, Hereditary 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).
Nephritis, Hereditary: A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (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 |
|---|---|
| Ignatova, MS | 2 |
| Fokeeva, VV | 1 |
| Degtiareva, EM | 1 |
| Iaroshevskaia, TI | 1 |
| Orlova, GI | 1 |
2 other studies available for pyridoxine and Nephritis, Hereditary
| Article | Year |
|---|---|
[Diagnosis and treatment of hereditary nephritis in children].
Topics: Adenosine Triphosphate; Adolescent; Child; Child, Preschool; Humans; Infant; Male; Nephritis, Heredi | 1976 |
[Treatment of hereditary nephritis in children].
Topics: Adenosine Triphosphate; Adrenal Cortex Hormones; Antimetabolites; Child; Humans; Nephritis, Heredita | 1976 |