niacin has been researched along with Amino Acid Metabolism Disorders, Inborn in 9 studies
Niacin: A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.
vitamin B3 : Any member of a group of vitamers that belong to the chemical structural class called pyridines that exhibit biological activity against vitamin B3 deficiency. Vitamin B3 deficiency causes a condition known as pellagra whose symptoms include depression, dermatitis and diarrhea. The vitamers include nicotinic acid and nicotinamide (and their ionized and salt forms).
nicotinic acid : A pyridinemonocarboxylic acid that is pyridine in which the hydrogen at position 3 is replaced by a carboxy group.
| 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 |
|---|---|
| DELAEY, P | 2 |
| HOOFT, C | 2 |
| TIMMERMANS, J | 2 |
| SNOECK, J | 2 |
| KOMROWER, GM | 1 |
| WILSON, V | 1 |
| CLAMP, JR | 1 |
| WESTALL, RG | 1 |
| FOIS, A | 1 |
| LECCHINI, L | 1 |
| MILNE, MD | 1 |
| ROSANOVA, AR | 1 |
| NEIMEYER, H | 1 |
| COMPALL, T | 1 |
| MICHAELSON, AS | 1 |
| Salih, MA | 1 |
| Bender, DA | 1 |
| McCreanor, GM | 1 |
| Voiculescu, V | 1 |
| Luca, N | 1 |
| Hategan, D | 1 |
| Goulon, M | 1 |
| Escourolle, R | 1 |
| Grosbuis, S | 1 |
| Caldera, R | 1 |
| Nouailhat, F | 1 |
| Barois, A | 1 |
9 other studies available for niacin and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. I. RESULTS OF INTRAVENOUS AND ORAL TRYPTOPHAN LOADING TESTS IN A CASE OF HARTNUP DISEASE.
Topics: Amino Acid Metabolism, Inborn Errors; Biomedical Research; Friedreich Ataxia; Genetics, Medical; Har | 1964 |
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Drug Therapy; Feces; Hartnup Disease; Humans; Indican; | 1964 |
HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Electrophoresis; Humans; Hydrolases; Ky | 1964 |
ACUTE CEREBELLAR ATAXIA ASSOCIATED WITH SOME FEATURES OF THE HARTNUP SYNDROME. PRESENTATION OF A CASE.
Topics: Amino Acid Metabolism, Inborn Errors; Cerebellar Ataxia; Child; Chromatography; Drug Therapy; Electr | 1964 |
DISORDERS OF AMINO-ACID TRANSPORT.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Cystinosis; Cystinuria; Dog Diseases; Dogs; Kidney Di | 1964 |
ENZYMES IN MENTAL RETARDATION.
Topics: Amino Acid Metabolism, Inborn Errors; Drug Therapy; Enzymes; Hepatolenticular Degeneration; Humans; | 1964 |
Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.
Topics: Amino Acid Metabolism, Inborn Errors; Cataract; Cerebellar Ataxia; Child, Preschool; Consanguinity; | 1985 |
Biochemical research in two cases of endogenous pellagra.
Topics: Adult; Alanine Transaminase; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartate Aminotrans | 1973 |
[Endogenous pellagra without hyperaminoaciduria].
Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography, Paper; Diagnosi | 1969 |