PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Symptom | |seizures |
| Sentences | 329 |
| PubMedID- 23825415 | The results of the present study reveal similarities in onset sites of spontaneous seizures in patients with temporal lobe epilepsy and pilocarpine-treated rats that support the model's validity. |
| PubMedID- 21480884 | Affected individuals have a form of genetic epilepsy with generalized seizures variably associated with mr. |
| PubMedID- 22937231 | Recent data suggest that temporal lobe epilepsy (tle), especially in patients with medically refractory seizures, may be a progressive, degenerative process. |
| PubMedID- 25945128 | In a more recent report, authors showed a frequency of 62% in amci and ad patients known to have epilepsy and 6% in patients without seizures . |
| PubMedID- 24351614 | Introduction: about 10% of seizures in children with epilepsy are typical absence seizures. |
| PubMedID- 25117208 | We investigated the effect of positive airway pressure (pap) therapy on seizures in adults with epilepsy referred to the cleveland clinic for polysomnography (psg) from 1997 to 2010. |
| PubMedID- 23248663 | In addition, this case illustrated that in patients with heart blocks and seizures, a diagnosis of epilepsy needs to be made with caution and such patients need further evaluations by a cardiologist or electrophysiologist to consider pacing and prevent future catastrophic events. |
| PubMedID- 25312505 | Various missense mutations of thenav1.1 channel (scn1a), which alter channel properties, have been reported ina familial syndrome of generalized epilepsy with febrile seizures plus (gefs+).scn1a-targeted rats carrying a missense mutation (n1417h) in the thirdpore region of the sodium channel were developed by gene-driven enu mutagenesis. |
| PubMedID- 22944210 | Generalized epilepsy with febrile seizures plus (gefs+) comprises a group of clinically and genetically heterogeneous epilepsy syndrome. |
| PubMedID- 24151464 | Between seizures the brain of patients with epilepsy generates pathological patterns of synchronous activity, designated as interictal epileptiform discharges (id). |
| PubMedID- 25849340 | Cortical areas colored yellow, orange, and red indicate thinner gm (in mm) per year of epilepsy in patients with hyp onset seizures, whereas areas colored blue, indigo, and violet correspond to reduced gm per year of epilepsy in patients with lvf onset seizures. |
| PubMedID- 21480876 | Purpose: mutations in the scn1a gene, which encodes the alpha1 subunit of voltage-gated sodium channels, cause generalized epilepsy with febrile seizures plus (gefs+) and severe myoclonic epilepsy of infancy (smei). |
| PubMedID- 20923578 | Well known examples are genetic generalized epilepsy with febrile seizures plus , caused by mutations in sodium channel genes, and recently, genetic generalized epilepsy caused by the 15q13.3 cnv . |
| PubMedID- 25378166 | Brain regions generating seizures in patients with refractory partial epilepsy are referred to as the epileptogenic zone (ez). |
| PubMedID- 24842605 | Generalised (genetic) epilepsy with febrile seizures plus (gefs+) is a familial epilepsy syndrome with various phenotypes. |
| PubMedID- 24350775 | These findings can be attributed to the coexistence of multiple seizure types in certain epileptic syndromes that exhibited a higher rate of drug-resistance or relapsing course, as for instance epilepsy with myoclonic-astatic seizures or epilepsy with myoclonic absence seizures. |
| PubMedID- 19563347 | Methods: epilepsy with spontaneous recurrent seizures (srs) was induced by status epilepticus. |
| PubMedID- 24009559 | In an attempt to prevent or reduce worsening of epilepsy-related co-morbidities together with attenuating epileptic seizures, it would be of interest to investigate the actions of vacht blockers, in animal models of epilepsy to confirm whether similar effects on seizures, epilepsy progression and cognitive functioning will be obtained as in the vacht knock-down mouse model. |
| PubMedID- 24002088 | epilepsy with petit mal seizures appeared at the age of 7 months. |
| PubMedID- 24339583 | A smaller proportion of patients with or without seizures due to epilepsy and se are likely to be due to intercurrent illness such as systemic infections or metabolic disturbances or changes in antiepileptic medication or some remote symptomatic etiology. |
| PubMedID- 26133327 | Doose syndrome, or epilepsy with myoclonic-atonic seizures, is a rare electroclinical syndrome. |
| PubMedID- PMC4033928 | The goal of eradication of all simple partial seizures for patients with lesional epilepsy (often from brain tumors) often leads to excessive aeds and accumulation of side effects from polytherapy. |
| PubMedID- 25751627 | Genes belong to neurotransmitter receptor families or other ion channels, genes were discussed by different research groups as putatively involved in epilepsy, genes are associated with seizures in animals or associated with human neurodevelopmental phenotypes, etc. |
| PubMedID- 20471324 | Idiopathic generalized epilepsy with generalized tonic-clonic seizures (ige-gtc): a population-based cohort with >20 year follow up for medical and social outcome. |
| PubMedID- 20887367 | The present data suggest that medical carbogen with 5% co(2) can be used for acute treatment to suppress seizures in epilepsy patients. |
| PubMedID- 26090323 | We present a 7-year-old girl who suffered from epilepsy with generalized tonic-clonic seizures and absence epilepsy. |
| PubMedID- 25422574 | A 41-year-old white woman developed epilepsy with focal seizures secondary to a left fronto-parietal atypical meningioma (grade ii world health organization). |
| PubMedID- 21314679 | This retrospective cross-sectional study was carried out to study the association between different levels of hyponatremia and the occurrence of epileptic seizures in patients without a prior epilepsy diagnosis. |
| PubMedID- 20659855 | As discussed, potential applications of these technologies include the early diagnosis of diseases such as congestive heart failure, the prevention of chronic conditions such as diabetes, improved clinical management of neurodegenerative conditions such as parkinson's disease, and the ability to promptly respond to emergency situations such as seizures in patients with epilepsy and cardiac arrest in subjects undergoing cardiovascular monitoring. |
| PubMedID- 21352605 | It has been reported that there is a relationship between gene polymorphism of crt, transport activity of crt, and neurological symptoms such as developmental delay, mental disorder and epilepsy with seizures . |
| PubMedID- 22787629 | Generalized epilepsy with febrile seizures plus (gefs+) is caused by missense mutations in nav1.1 channels, which have variable functional effects on sodium channels expressed in non-neuronal cells, but may primarily cause loss of function when expressed in mice. |
| PubMedID- 23930253 | Considering the small number of case-control studies conducted on the investigation of the effect of the natural progesterone on controlling the catamenial seizures in women with catamenial epilepsy and according to undesirable severe side effects of using different doses of natural progesterone, more studies with higher sample volume and with different doses of progesterone are suggested to be done in these patients. |
| PubMedID- 20600615 | Novel mutation of scn1a in familial generalized epilepsy with febrile seizures plus. |
| PubMedID- 22220564 | Purpose: to accurately determine the frequency and nature of the family history of seizures in patients with benign childhood epilepsy with centrotemporal spikes (bects). |
| PubMedID- 24339590 | epilepsy may provoke seizures related to transcranial stimulation. |
| PubMedID- 22457775 | A locus at cfa37 predisposes belgian shepherds to focal epilepsy with seizures originating from multiple cerebral lobes and without any detectable cerebral lesions on mri studies. |
| PubMedID- 23739109 | These were first used to control seizures in children with intractable epilepsy, but in recent years have also been demonstrated to be safe and effective in children and adults with a broad range of seizure types and are being used with increased frequency worldwide. |
| PubMedID- 23267335 | Key clues about focused attention, and also unifying constraints and response dependencies (to be explained further), stem from initial investigations into the so-called “split-brain.” the medical puzzle of how to ameliorate the bilateral spread of seizures associated with intractable epilepsy led to the procedure which involves surgical separation of the left and right sides of the cerebral forebrain commissures. |
| PubMedID- 21704126 | Genetic epilepsy with febrile seizures plus (gefs+) is a familial autosomal dominant condition characterized by genetic heterogeneity. |
| PubMedID- 24649474 | In all cases, the patients suffered from medically refractory epilepsy with seizures determined to originate from temporal neocortex or mesiotemporal areas, and were using at least two anti-epileptic drugs (aed) at the time of surgery. |
| PubMedID- 25590135 | They generate a wide spectrum of phenotypes ranging from the relatively mild generalized epilepsy with febrile seizures plus (gefs+) to other severe epileptic encephalopathies, including myoclonic epilepsy in infancy (smei), cryptogenic focal epilepsy (cfe), cryptogenic generalized epilepsy (cge) and a distinctive subgroup termed as severe infantile multifocal epilepsy (simfe). |
| PubMedID- 20671980 | reported the utility of the assumption of antiepileptic drugs in conversion patients with no epileptic seizures associated with epilepsy, but in our case the presence of epilepsy was excluded. |
| PubMedID- 23808728 | epilepsy, especially with refractory seizures, is thought to arise only from cortical lesions or substrate. |
| PubMedID- 21156207 | Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus. |
| PubMedID- 22218271 | Suggestive evidence of linkage in this region was also found for epilepsy with generalized tonic-clonic seizures (p = 0.0034). |
| PubMedID- 21167825 | However, little is known about the changes in the functional architecture of the rsns in idiopathic generalized epilepsy patients with generalized tonic-clonic seizures (gtcs). |
| PubMedID- 20452746 | Generalized epilepsy with febrile seizures plus (gefs+) spectrum: clinical manifestations and scn1a mutations in indonesian patients. |
| PubMedID- 25532859 | One, carrying a novel de novo deletion had epilepsy with myoclonic-atonic seizures (mae), mild slowing of head growth, choreiform movements and developmental delay. |
| PubMedID- 20628201 | Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus. |
| PubMedID- 26307329 | This has been defined as epilepsy with persistent seizures despite adequate trials of at least two anti-epileptic drugs (aeds). |