pteridines has been researched along with Diseases, Metabolic in 3 studies
| 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 Diseases, Metabolic
| 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 |