In other words, when the subgroup of patients with MTS-TLE and drug resistant seizures is examined history of childhood febrile seizure loses its value as a distinguishing factor

structures, and temporal lobe epilepsy: An MRI volumetric study Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial. This information is current as of June

Patients with a posterior mesial temporal lobe seizure onset are more likely to experience persistent postoperative seizures relative to patients with an anterior mesial

Table 3 Clinical characteristics of patients with newly diagnosed mesial temporal lobe epilepsy and hippocampal atrophy.. a Immediate responders never had another seizure after

The international league against epilepsy defines febrile seizure as a seizure occurring in childhood after one month of age associated with febrile illness that

It has recently been reported a case of left mesial temporal lobe epilepsy due to hippocampal sclerosis, with concordant MRI and EEG, presenting with a seizure semiology

Patients with mesial temporal lobe epilepsy demonstrated discrete fast oscillations consistently in areas of seizure onset, and we postulate that when HFOs occur early during

RESULTS: The patients with mesial temporal lobe epilepsy showed decreased homotopic connectivity in the mesial temporal structures, temporal pole, and striatum.. Alterations of

FMTLE familial mesial temporal lobe epilepsy FSEC familial spontaneous epileptic cats FTLE familial temporal lobe epilepsy GAD glutamic acid decarboxylase HS hippocampal sclerosis

In the current study, we observed that about one-fifth of the patients who had MTS in their MRI and responded well to standard anterior temporal lobectomy reported auras that

Thus, high-signal area in MR of the mesial temporal lobe can be said to be common in patients with the onset of tem- poral lobe epilepsy in childhood and in patients with history

MTLE-HS = Mesial temporal lobe epilepsy with hippocampal sclerosis, CNLs = Calcified neurocysticercotic

Potential outcome predictors, including gender, age at surgery, duration of epilepsy, race, history of status epilepticus before surgery, history of tonic-clonic seizures

Abbreviations for Childhood Epilepsy Panel (CHE78): ADLTE: Autosomal Dominant Lateral Temporal lobe Epilepsy ADNFLE: Autosomal Dominant Nocturnal Frontal lobe Epilepsy AHC:

Objective: Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS) is a common epilepsy syndrome often poorly controlled by antiepileptic drug (AED)

The differential diagnosis of fMTLE include lateral temporal lobe epilepsy, GEFS+, febrile seizures (FS), familial partial epilepsy with variable foci (FPEVF), and

Functional Neuroscience. Dartmouth Medical School: Dartmouth Medical School. Prefrontal hypofunction in patients with intractable mesial temporal lobe epilepsy. Two systems of

Febrile seizures are a common childhood seizure disorder and a defining feature of genetic epilepsy with febrile seizures plus (GEFS+), a syndrome frequently associated with Na