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Dravet syndrome: Advances in etiology, clinical presentation, and treatment.
He Z, Li Y, Zhao X, Li B. He Z, et al. Epilepsy Res. 2022 Dec;188:107041. doi: 10.1016/j.eplepsyres.2022.107041. Epub 2022 Oct 29. Epilepsy Res. 2022. PMID: 36368227 Review.
Most DS patients experience prolonged, hemiclonic or tonic-clonic seizures triggered by fever during the first year of life, followed by the gradual onset of other seizure types, including myoclonic, atypical absence, and focal seizures. Over ti …
Most DS patients experience prolonged, hemiclonic or tonic-clonic seizures triggered by fever during the first year of life, f …
Dravet Syndrome: Diagnosis and Long-Term Course.
Connolly MB. Connolly MB. Can J Neurol Sci. 2016 Jun;43 Suppl 3:S3-8. doi: 10.1017/cjn.2016.243. Can J Neurol Sci. 2016. PMID: 27264139 Review.
The typical presentation is characterized by hemiclonic or generalized clonic seizures triggered by fever during the first year of life, followed by myoclonic, absence, focal and generalized tonic-clonic seizures. ...Early diagnosis is important to avo …
The typical presentation is characterized by hemiclonic or generalized clonic seizures triggered by fever during the first yea …
Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects.
Verrotti A, Soldani C, Laino D, d'Alonzo R, Grosso S. Verrotti A, et al. World J Pediatr. 2014 May;10(2):108-13. doi: 10.1007/s12519-014-0478-9. Epub 2014 May 7. World J Pediatr. 2014. PMID: 24801229 Review.
DATA SOURCES: Based on recent original publications, we have reviewed the different types of seizures and EEG findings in PWS patients, the response to antiepileptic treatment, and the prognosis of epilepsy. RESULTS: The frequency of epilepsy in PWS patients ranges from 4% …
DATA SOURCES: Based on recent original publications, we have reviewed the different types of seizures and EEG findings in PWS patient …
Acute encephalitis with refractory, repetitive partial seizures.
Sakuma H. Sakuma H. Brain Dev. 2009 Aug;31(7):510-4. doi: 10.1016/j.braindev.2009.02.010. Epub 2009 Mar 26. Brain Dev. 2009. PMID: 19327924 Review.
Seizures in AERRPS are almost exclusively of localized origin, whose semiology includes eye deviation, hemifacial twitching, hemiclonic convulsion, and autonomic manifestations. ...They are extremely pharmaco-resistant and are only suppressed by intravenous a
Seizures in AERRPS are almost exclusively of localized origin, whose semiology includes eye deviation, hemifacial twitching,
Diagnosis and long-term course of Dravet syndrome.
Scheffer IE. Scheffer IE. Eur J Paediatr Neurol. 2012 Sep;16 Suppl 1:S5-8. doi: 10.1016/j.ejpn.2012.04.007. Epub 2012 Jun 16. Eur J Paediatr Neurol. 2012. PMID: 22704920 Review.
A healthy, developmentally normal infant presents at around 6 months of age with convulsive status epilepticus, which may be hemiclonic or generalized; seizures may be triggered by fever, illness or vaccination. The infant typically has further episodes of status ep …
A healthy, developmentally normal infant presents at around 6 months of age with convulsive status epilepticus, which may be hemiclonic