pteridines has been researched along with Spasms, Infantile in 2 studies
Spasms, Infantile: An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Macaya, A | 1 |
| Brunso, L | 1 |
| Fernández-Castillo, N | 1 |
| Arranz, JA | 1 |
| Ginjaar, HB | 1 |
| Cuenca-León, E | 1 |
| Corominas, R | 1 |
| Roig, M | 1 |
| Cormand, B | 1 |
| Slot, HM | 1 |
| Overweg-Plandsoen, WC | 1 |
| Bakker, HD | 1 |
| Abeling, NG | 1 |
| Tamminga, P | 1 |
| Barth, PG | 1 |
| Van Gennip, AH | 1 |
2 other studies available for pteridines and Spasms, Infantile
| Article | Year |
|---|---|
Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study.
Topics: Carbon-Carbon Lyases; Coenzymes; DNA Mutational Analysis; Exons; Humans; Infant; Male; Metalloprotei | 2005 |
Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsions.
Topics: Amino Acids; Brain; Brain Diseases; Calcinosis; Chorionic Villi Sampling; Coenzymes; Female; Humans; | 1993 |