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PedAM

Pediatric Disease Annotations & Medicines




Disease epilepsy
Symptom |seizures
Sentences 329
PubMedID- 21488289 Disease: generalized epilepsy with febrile seizures plus.
PubMedID- 23586701 Mutations in this gene are frequently found in dravet syndrome (ds), and are sometimes found in genetic epilepsy with febrile seizures plus (gefs+), migrating partial seizures of infancy (mpsi), other infantile epileptic encephalopathies, and rarely in infantile spasms.
PubMedID- 25795284 These range from severe phenotypes including dravet syndrome to milder phenotypes such as genetic epilepsy with febrile seizures plus (gefs+).
PubMedID- 24199829 An epilepsy patient with recurring sensorimotor seizures involving the left hand every 10 min, was imaged with a hyperspectral camera during surgery.
PubMedID- 24480790 Mutations in gabrg2, which encodes the gamma2 subunit of gabaa receptors, can cause both genetic epilepsy with febrile seizures plus (gefs+) and dravet syndrome.
PubMedID- 24600432 While numerous treatment options are available to control seizures associated with epilepsy, approximately 20–30% of epileptic patients are resistant to treatment.
PubMedID- 20413804 In 2006, intravenous levetiracetam received us food and drug administration (fda) approval for adjunctive treatment of partial onset seizures in adults with epilepsy, 16 years or older.
PubMedID- 20446062 Uncontrolled epilepsy, particularly with generalized tonic-clonic seizures, appears to be the most highly associated modifiable risk factor for sudep.
PubMedID- 23223299 Neonatal seizures can lead to later life epilepsy and neurobehavioral deficits, and there are no treatments to prevent these sequelae.
PubMedID- 23409712 Absence epilepsy is associated with generalized epileptic seizures which concerns 10% of population suffering from epilepsy.
PubMedID- 22644603 He developed epilepsy with generalized seizures and was treated with phenobarbital; eeg was normal.
PubMedID- 23861864 We have also shown how seizures, when associated with epilepsy were considered an innate, traditional illness, thought to require traditional treatment.
PubMedID- 25154221 In 50 to 80% of the epilepsy patients with tsc, epileptic seizures become resistant against anti-epileptic medications.
PubMedID- 25901181 In addition, the patient was suffering from treatment-resistant epilepsy with generalized tonic-clonic seizures (gtcs), often in series, with onset at about 1 year-of-age.
PubMedID- 24663110 Nearly a year after the asp event, an 84 years old male survivor re-experienced severe seizures and was diagnosed with temporal lobe epilepsy caused by domoic acid intoxication 8.
PubMedID- 25524373 A novel kcnq3 mutation in familial epilepsy with focal seizures and intellectual disability.
PubMedID- 25206388 Sodium channel α1 subunit mutations have also been found in generalized epilepsy with febrile seizures plus, infantile spasms and severe epilepsy of infancy5.
PubMedID- 22480923 Purpose: to review the legislation for non-commercial driving licenses in the western world for unprovoked first seizures (ufs) and recurrence of established epilepsy, and to examine available evidence on the road traffic accident (rta) risk in people with seizures.
PubMedID- 20406251 The best results were obtained in idiopathic generalized epilepsy (ige) patients with seizures habitually triggered by typical factors (sleep deprival, alcohol) but also some others were successful.
PubMedID- 23874432 Demonstrated that statistical or spectral textural features outperformed visual assessment in discriminating between tumors, as well as in discerning subtle anatomic changes associated with a high risk of seizures in patients with epilepsy –.
PubMedID- 25410361 Still, seizures in about 30% of patients with epilepsy are not adequately controlled, or the drugs cause quality-of-life-compromising adverse events.
PubMedID- 20634145 Of these, 43 (4.0%) were "redos." the most common indication for repeat video/eeg monitoring was evidence of focal epilepsy with no recorded seizures, followed by normal interictal eeg with no recorded episodes.
PubMedID- 20418066 Forty-five of these 97 patients also had seizures consistent with benign focal epilepsy of childhood with centrotemporal spikes (bects).
PubMedID- 20478766 Both had temporal lobe epilepsy with resolution of seizures after a temporal lobectomy.
PubMedID- 21095488 Eligible patients were required to have epilepsy with partial-onset seizures, treated with a stable regimen of 1 or 2 antiepileptic drugs.
PubMedID- 26042039 For example, for scn1b mutations related to cns diseases, a single mutant allele may result in the development of a milder disease like generalized epilepsy with febrile seizures plus.
PubMedID- 25053257 Early seizures are predictors of future epilepsy in stroke patients , although a study by bladin and colleagues 4 showed that all of the patients that had late onset seizures, which were those at 2 or more weeks after the stroke, developed epilepsy.
PubMedID- 23653425 Dravet syndrome is an infantile epilepsy syndrome with intractable pleomorphic seizures, cognitive impairment, and a number of comorbidities including ataxia/gait abnormalities and behavioral issues.
PubMedID- 24985894 Kainate-induced seizures constitute a model of temporal lobe epilepsy where prominent changes are observed in the hippocampal neuropeptide y (npy) system.

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