PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0162635|angelman syndrome |
| Sentences | 4 |
| PubMedID- 24796722 | Objective: neurological manifestations including psychomotor developmental delay and epilepsy in patients with angelman syndrome caused by ubiquitin protein ligase e3a (ube3a) mutations has been considered similar but is relatively milder than that in patients with deletion-type angelman syndrome. |
| PubMedID- 20398390 | epilepsy in patients with angelman syndrome. |
| PubMedID- 22779920 | Methods: a pediatric angelman syndrome cohort with refractory epilepsy was treated with the lgit and followed prospectively over 4 months. |
| PubMedID- 24764755 | Phenotypic findings similar to the angelman syndrome, with asd, epilepsy and behavioral problems. |
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