Page last updated: 2024-10-20

pyridoxine and Alport Syndrome

pyridoxine has been researched along with Alport Syndrome 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).

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ignatova, MS2
Fokeeva, VV1
Degtiareva, EM1
Iaroshevskaia, TI1
Orlova, GI1

Other Studies

2 other studies available for pyridoxine and Alport Syndrome

ArticleYear
[Diagnosis and treatment of hereditary nephritis in children].
    Pediatriia, 1976, Issue:9

    Topics: Adenosine Triphosphate; Adolescent; Child; Child, Preschool; Humans; Infant; Male; Nephritis, Heredi

1976
[Treatment of hereditary nephritis in children].
    Sovetskaia meditsina, 1976, Issue:10

    Topics: Adenosine Triphosphate; Adrenal Cortex Hormones; Antimetabolites; Child; Humans; Nephritis, Heredita

1976