Disease | dystonia |
Phenotype | C0014544|epilepsy |
Sentences | 5 |
PubMedID- 26245188 | Psychogenic non-epileptic seizures, sleep disorders, syncope, dystonia), patients with a doubtful epilepsy diagnosis, patients who had only a single seizure, and patients with a severe mental retardation. |
PubMedID- 22613698 | Steroid-responsive focal epilepsy with focal dystonia accompanied by glutamate receptor delta2 antibody. |
PubMedID- 20213496 | The tottering phenotype, an autosomal recessive mouse disease, is associated with mild ataxia, spontaneous behavioral arrest associated with synchronous, bilateral cortical polyspike discharges (resembling human absence epilepsy), and attacks of paroxysmal dystonia [10, 61]. |
PubMedID- 26088892 | Myoclonic occipital photosensitive epilepsy with dystonia (moped): a familial epilepsy syndrome. |
PubMedID- 21087195 | Early-onset progressive myoclonic epilepsy with dystonia mapping to 16pter-p13.3. |
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