PedAM
Pediatric Disease Annotations & Medicines
| Disease | rett syndrome |
| Phenotype | C0014544|epilepsy |
| Sentences | 10 |
| PubMedID- 25346641 | What you seize is what you get: do we yet understand epilepsy in rett syndrome. |
| PubMedID- 20491871 | epilepsy in rett syndrome---the experience of a national rett center. |
| PubMedID- 22998673 | epilepsy in rett syndrome, and cdkl5- and foxg1-gene-related encephalopathies. |
| PubMedID- 26089674 | Management of epilepsy in patients with rett syndrome: perspectives and considerations. |
| PubMedID- 22946725 | They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the pcdh 19 gene. |
| PubMedID- 25789914 | epilepsy in rett syndrome--lessons from the rett networked database. |
| PubMedID- 23583050 | Our goal in this review is to better define the clinical and electrophysiological aspects of the epilepsy associated with rett syndrome and provide practical guidance regarding management. |
| PubMedID- 23421866 | Aim: the aim of this study was to identify characteristics of epilepsy in rett syndrome (rtt), and relationships between epilepsy and genotype. |
| PubMedID- 21764336 | epilepsy in rett syndrome: association between phenotype and genotype, and implications for practice. |
| PubMedID- 20728410 | epilepsy in rett syndrome: clinical and genetic features. |
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