pteridines has been researched along with Acquired Metabolic Diseases, Brain in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Ogier, H | 1 |
| Saudubray, JM | 1 |
| Charpentier, C | 1 |
| Munnich, A | 1 |
| Perignon, JL | 1 |
| Kesseler, A | 1 |
| Frezal, J | 1 |
| Appignani, BA | 1 |
| Kaye, EM | 1 |
| Wolpert, SM | 1 |
| Salvan, AM | 1 |
| Chabrol, B | 1 |
| Lamoureux, S | 1 |
| Confort-Gouny, S | 1 |
| Cozzone, PJ | 1 |
| Vion-Dury, J | 1 |
3 other studies available for pteridines and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum].
Topics: Brain Diseases, Metabolic; Coenzymes; Consanguinity; Female; Humans; Infant; Metalloproteins; Molybd | 1982 |
CT and MR appearance of the brain in two children with molybdenum cofactor deficiency.
Topics: Atrophy; Brain; Brain Diseases, Metabolic; Coenzymes; Diagnosis, Differential; Female; Follow-Up Stu | 1996 |
In vivo brain proton MR spectroscopy in a case of molybdenum cofactor deficiency.
Topics: Brain; Brain Diseases, Metabolic; Coenzymes; Genes, Recessive; Humans; Infant, Newborn; Magnetic Res | 1999 |