pteridines has been researched along with Infant, Newborn, Diseases in 2 studies
Infant, Newborn, Diseases: Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zaki, MS | 1 |
| Selim, L | 1 |
| El-Bassyouni, HT | 1 |
| Issa, MY | 1 |
| Mahmoud, I | 1 |
| Ismail, S | 1 |
| Girgis, M | 1 |
| Sadek, AA | 1 |
| Gleeson, JG | 1 |
| Abdel Hamid, MS | 1 |
| Sass, JO | 1 |
| Gunduz, A | 1 |
| Araujo Rodrigues Funayama, C | 1 |
| Korkmaz, B | 1 |
| Dantas Pinto, KG | 1 |
| Tuysuz, B | 1 |
| Yanasse Dos Santos, L | 1 |
| Taskiran, E | 1 |
| de Fátima Turcato, M | 1 |
| Lam, CW | 1 |
| Reiss, J | 1 |
| Walter, M | 1 |
| Yalcinkaya, C | 1 |
| Camelo Junior, JS | 1 |
2 other studies available for pteridines and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.
Topics: Amino Acid Metabolism, Inborn Errors; Coenzymes; Egypt; Humans; Infant, Newborn; Infant, Newborn, Di | 2016 |
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
Topics: Amino Acid Metabolism, Inborn Errors; Brazil; Coenzymes; Diagnosis, Differential; DNA Mutational Ana | 2010 |