PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Symptom | |seizures |
| Sentences | 329 |
| PubMedID- 21167748 | Is temporal lobe epilepsy with childhood febrile seizures a distinctive entity. |
| PubMedID- 24627806 | Hypothesized that the atkins diet can induce metabolic ketosis and might reduce seizures in patients with epilepsy, similar to the ketogenic diet . |
| PubMedID- 22406087 | Ring chromosome 20 syndrome is a rare chromosomal disorder characterized by refractory epilepsy, with seizures in wakefulness and sleep, behavioral problems and mild to severe cognitive impairment. |
| PubMedID- 22292491 | Purpose: a mutation in the beta(1) subunit of the voltage-gated sodium (na(v)) channel, beta(1) (c121w), causes genetic epilepsy with febrile seizures plus (gefs+), a pediatric syndrome in which febrile seizures are the predominant phenotype. |
| PubMedID- 21425109 | Results: nine patients presented generalised epilepsy with febrile seizures plus; six had dravet's syndrome; six had borderline dravet's syndrome; two had doose's syndrome; and three of them had cryptogenic partial epilepsy. |
| PubMedID- 23404539 | Kd not only effectively alleviates clinical seizures in patients with epilepsy, but also improves electroencephalographic (eeg) features (9–10). |
| PubMedID- 23015297 | Scn1a mutations can also cause genetic epilepsy with febrile seizures plus (gefs+), severe myoclonus epilepsy of infancy (smei) and some other rare epilepsy syndromes . |
| PubMedID- 24204362 | Lev has been found to be particularly beneficial for restraining seizures in animal models of spontaneous epilepsy, acute seizures, and status epilepticus (se). |
| PubMedID- 23323135 | Other seizure phenotypes were also observed: gefs+, febrile seizure, myoclonic astatic epilepsy, generalized epilepsy with tonic/clonic seizures, and partial epilepsy.1,2 subsequent animal studies have shown that a good animal model of familial cae can be created with this heterozygotic mutation.24,25 nevertheless, this mutation has not been reproduced in either unrelated sporadic individuals or in other ethnic groups. |
| PubMedID- 25917466 | Genetic epilepsy with febrile seizures plus (gefs+) is a complex autosomal dominant disorder usually caused by mutations in scn1a (a voltage-gated sodium channel). |
| PubMedID- 25884503 | It was recently renamed as epilepsy with myoclonic-atonic seizures and classified as one of the childhood onset electroclinical syndromes 6. |
| PubMedID- 23447651 | The final diagnosis was reflex epilepsy with partial simple seizures (sharp pain) elicited by tactile stimuli. |
| PubMedID- 22822044 | Neural stimulation can reduce the frequency of seizures in persons with epilepsy, but rates of seizure-free outcome are low. |
| PubMedID- 19620139 | Conclusion: besides reading-induced myoclonic jerks of the jaw, a second variant of reading epilepsy exists with clearly partial seizures manifested by visual symptoms and a- or dyslexia. |
| PubMedID- 26271793 | The most common epileptic encephalopathies are ohtahara syndrome, early myoclonic encephalopathy, epilepsy of infancy with migrating focal seizures, west syndrome and dravet syndrome, which are usually unresponsive to traditional antiepileptic medication. |
| PubMedID- 23583052 | epilepsy with myoclonic-atonic seizures is characterized by myoclonic-atonic, absence, tonic-clonic, and eventually tonic seizures, appearing in previously normal children at ages 18-60 months. |
| PubMedID- 26166592 | The generalized type is the most common form of epilepsy, with tonic-colonic seizures being the most frequent type in our area. |
| PubMedID- 22251930 | In this study we determined the time between onset of seizures and awakening in patients with frontal lobe epilepsy (fle) and temporal lobe epilepsy (tle). |
| PubMedID- 24277604 | Generalized epilepsy with febrile seizures plus (gefs+) is an autosomal dominant disorder in which subjects have febrile seizures early in childhood, with increased risk for febrile and afebrile seizures later on in life. |
| PubMedID- 25205163 | We excluded patients with nonepileptic seizures, progressive cause of epilepsy, or not keeping a seizure record. |
| PubMedID- 20735403 | Similar selectivity was observed for ranolazine block of increased persistent current exhibited by na(v) 1.1 channel mutations representing three distinct clinical syndromes, generalized epilepsy with febrile seizures plus (r1648h, t875m), severe myoclonic epilepsy of infancy (r1648c, f1661s) and familial hemiplegic migraine type 3 (l263v, q1489k). |
| PubMedID- 21789280 | Chronic epilepsy with recurrent generalized seizures is known to be associated with a high risk of sudep . |
| PubMedID- 20450160 | 13, 1315-1319 as a heritable susceptibility allele for generalized epilepsy with febrile seizures plus, are also potentiated by these dhpms. |
| PubMedID- 24339575 | It is recommended that first-aid management of seizures in epilepsy should be a part of school curriculum. |
| PubMedID- 23433109 | In general, stress is among the most frequently self-reported precipitant of seizures in patients with epilepsy (1-3). |
| PubMedID- 21450442 | Measurement and quantification of generalized tonic-clonic seizures in epilepsy patients by means of accelerometry--an explorative study. |
| PubMedID- 21086729 | Types of seizures in patients with epilepsy were different from seizures provoked by brain tumors. |
| PubMedID- 23405072 | Tsc is one of the leading causes of genetic epilepsy with seizures affecting almost 90% of affected individuals 2. |
| PubMedID- 23994912 | epilepsy started with nocturnal seizures in 48% cases, in 30.5% of patients all seizures persisted during sleep. |
| PubMedID- 21453354 | Purpose: patients with recurrent epileptic seizures after the development of psychosis (psychosis-epilepsy) have been regarded as belonging to a different clinical entity from those with epilepsy antedating the development of psychosis (epilepsy-psychosis). |
| PubMedID- 21359874 | Cacna1a and episodic ataxia; scna1a and generalised epilepsy with febrile seizures plus (gefs+). |
| PubMedID- 20602059 | Conclusion: the reported cases suggest that dom pedro i's family presented epilepsy with tonic-clonic generalized seizures, besides psychogenic, organic non epileptic events and acute symptomatic seizures. |
| PubMedID- 25152725 | The aim of this study was to determine whether the reduction of seizures in patients with intractable epilepsy after self-regulation of slow cortical potentials (scps) was maintained almost 10 years after the end of treatment. |
| PubMedID- 22783167 | Mutations of gabaa and na+ channels can lead to familial forms of generalized epilepsy with complex febrile seizures gefs+; (scheffer and berkovic, 1997; spampanato et al., 2004; nakayama, 2009). |
| PubMedID- 20658245 | However, our study population may also be biased towards assertive and goal-seeking personality traits, and this would imply that in the general epilepsy population with seizures coping styles might be even more skewed towards the passive. |
| PubMedID- 25799588 | Ketogenic diets use long-chain fatty acids (lcfas, ≥ 16 carbon atoms) including palmitic acid and stearic acid and/or medium-chain triglycerides (mcts, 8–14 carbon atoms) to improve seizures in patients with intractable epilepsy . |
| PubMedID- 25567098 | In particular, an equivalent mutation (c121w) in β1 causes generalized epilepsy with febrile seizures plus (gefs+). |
| PubMedID- 24955329 | Mutations in the voltage-gated sodium-channel gene alpha subunit (scn1a) were discovered in an epileptic syndrome called genetic epilepsy with febrile seizures plus (gef +) including some patients with severe myoclonic epilepsy of infancy (smei) in gef + families . |
| PubMedID- 25250063 | Eight were affected by epilepsy with focal seizures, in seven cases symptomatic and in one case idiopathic. |
| PubMedID- 26361221 | (2012) created a fly knock-in model of human generalized epilepsy with febrile seizures plus (gefs+), a wide-spectrum disorder characterized by fever-associated seizing in childhood and lifelong affliction. |
| PubMedID- 23844283 | The same can be said of the transition states between nrem and rem sleep, which are activators in epilepsy with generalized tonic-clonic seizures, myoclonic epilepsy, and absences. |
| PubMedID- 22961543 | The severity of channel impairment has been suggested to underlie the different efficacies of some anti-epileptic drugs in treating either generalized epilepsy with febrile seizures plus or severe myoclonic epilepsy of infancy, of which many act through inhibiting vgscs. |
| PubMedID- 22315994 | The other patients have recurrent epilepsy, including 156 with tonic-clonic seizures and 39 with partial seizures. |
| PubMedID- 23274350 | In a second risk period (day 8-30), there was a non-significant increased risk of seizures in people without epilepsy (1.11, 0.73 to 1.70) but no increase in risk for those with epilepsy (1.00, 0.83 to 1.21). |
| PubMedID- 26484865 | Although more than 20 antiepileptic drugs (aeds) have been used to control seizures in patients with epilepsy, one-third of patients are resistant to treatment . |
| PubMedID- 26450065 | In addition, a significant increased serum level of il-6, and total numbers of leukocytes, lymphocytes, neutrophils, and natural killer cells were measured during the first minutes of the postictal phases after seizures in patients with temporal lobe epilepsy . |
| PubMedID- 25984652 | The duration of seizures in patients with drug-resistant epilepsy (ranging from 2 to 32 years in discovery and training phases, from 2 to 39 years in validation phase) was significantly longer than that in patients with drug-responsive epilepsy (ranging from 1 to 30 years in discovery and training phases, from 1 to 20 years in validation phase) (p < 0.001). |
| PubMedID- 25505320 | Previous studies suggest that spontaneous seizures in patients with temporal lobe epilepsy might be preceded by increased action potential firing of hippocampal neurons. |
| PubMedID- 22802792 | The reported case concerned drug-resistant epilepsy manifesting itself with everyday seizures in the number reaching a few dozens a day, in a boy with cortical dysplasia. |
| PubMedID- 24883310 | In 2011, liu investigated the wm differences between normal controls and two subsets of ige, juvenile myoclonic epilepsy and ige with generalized tonic-clonic seizures only. |