phenytoin has been researched along with Amelogenesis Imperfecta in 1 studies
Amelogenesis Imperfecta: A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (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 |
---|---|
Petermöller, M | 1 |
Kunze, J | 1 |
Gross-Selbeck, G | 1 |
1 other study available for phenytoin and Amelogenesis Imperfecta
Article | Year |
---|---|
Kohlschütter syndrome: syndrome of epilepsy--dementia--amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Brain; Dementia; Epilepsy; Female; Humans; Infant; Male; Phenytoin; Psychom | 1993 |