pteridines has been researched along with Metabolic Diseases in 3 studies
Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (100.00) | 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 |
|---|---|
| Slot, HM | 1 |
| Overweg-Plandsoen, WC | 1 |
| Bakker, HD | 1 |
| Abeling, NG | 1 |
| Tamminga, P | 1 |
| Barth, PG | 1 |
| Van Gennip, AH | 1 |
| Graf, WD | 1 |
| Oleinik, OE | 1 |
| Jack, RM | 1 |
| Weiss, AH | 1 |
| Johnson, JL | 1 |
| Reiss, J | 1 |
| Dorche, C | 1 |
| Stallmeyer, B | 1 |
| Mendel, RR | 1 |
| Cohen, N | 1 |
| Zabot, MT | 1 |
3 other studies available for pteridines and Metabolic Diseases
| Article | Year |
|---|---|
Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsions.
Topics: Amino Acids; Brain; Brain Diseases; Calcinosis; Chorionic Villi Sampling; Coenzymes; Female; Humans; | 1993 |
Ahomocysteinemia in molybdenum cofactor deficiency.
Topics: Brain; Brain Diseases; Coenzymes; Homocysteine; Humans; Infant; Magnetic Resonance Imaging; Metaboli | 1998 |
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B.
Topics: Carbon-Carbon Lyases; Cell Line; Coenzymes; Exons; Fibroblasts; Genotype; Humans; Metabolic Diseases | 1999 |