pyridoxine has been researched along with Amino Acid Transport Disorder, Neutral in 9 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).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (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 |
|---|---|
| Snyderman, SE | 1 |
| Grimm, U | 1 |
| Knapp, A | 1 |
| Schmitz, W | 1 |
| Smetan, M | 1 |
| Schmitz, KW | 1 |
| Reddemann, H | 1 |
| Schulz, M | 1 |
| Schlenzka, K | 1 |
| Korzon, M | 1 |
| Korzon, T | 1 |
| Dickerson, JW | 1 |
| Wiryanti, J | 1 |
| Holtzman, NA | 1 |
| Bartelheimer, HK | 2 |
| Grüttner, R | 2 |
| Simon, HA | 1 |
| Tabolin, VA | 1 |
| Kruglov, BV | 1 |
| Lebedev, VP | 1 |
| Levitina, NO | 1 |
| Antener, I | 1 |
| Rybak, C | 1 |
| Lambertz, J | 1 |
| Paupe, J | 1 |
| Bertaud, J | 1 |
| Vialatte, J | 1 |
4 reviews available for pyridoxine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
The dietary therapy of inherited metabolic disease.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C | 1975 |
[Clinical importance of tryptophan metabolism disorders].
Topics: Amino Acid Metabolism, Inborn Errors; Hartnup Disease; Humans; Neoplasms; Pyridoxine; Tryptophan; Tr | 1978 |
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
[Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Carboxy-Lyases; Child; Child, Preschool; Diabetes | 1972 |
5 other studies available for pyridoxine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
[Tryptophan metabolism and oligophrenia (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Down Syndrome; Epilepsy; Hartnup Disease; Humans; Intellectual | 1978 |
Pellagra and mental disturbance.
Topics: Animals; Brain; Diet; Hartnup Disease; Humans; Mental Disorders; Nicotinic Acids; Pellagra; Pyridoxi | 1978 |
[Hartnup syndrome. I. Diagnosis, therapy and clinical course].
Topics: Adolescent; Cerebellar Ataxia; Diagnosis, Differential; Dietary Proteins; Electroencephalography; Ha | 1971 |
[Hartnup disease (author's transl)].
Topics: Adolescent; Amino Acids; Child; Feces; Female; Hartnup Disease; Hippurates; Histidine; Humans; Malab | 1973 |
[Pellagroid syndrome with pseudo-myopathic signs cured with pyridoxine].
Topics: Child, Preschool; Diagnosis, Differential; Female; Hartnup Disease; Humans; Infant; Lupus Erythemato | 1970 |