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1 plex-partial seizures) or unimpaired (simple-partial seizures).
2 for tonic-clonic seizures than they are for partial seizures.
3 temporal and parietal regions than in simple partial seizures.
4 of 56 patients with drug-resistant, complex partial seizures.
5 y complex partial seizures and lastly simple partial seizures.
6 during complex-partial compared with simple-partial seizures.
7 ly greater in complex-partial than in simple-partial seizures.
8 set of obvious chronic recurrent spontaneous partial seizures.
9 cquired non-progressive cerebral lesions and partial seizures.
10 ity in up to 80% of patients with refractory partial seizures.
11 e epilepsy and medically intractable complex partial seizures.
12 lobe structures of 21 patients with complex partial seizures.
13 ages in 36 patients with intractable complex partial seizures.
14 ity in a rat model of focally evoked complex partial seizures.
17 tion, of cerebral tissue in 10 patients with partial seizures and acquired lesions and 30 patients wi
18 vulsive state expressed mainly by continuous partial seizures and even new bouts of generalized seizu
19 in opioid neurotransmission associated with partial seizures and higher cognitive function, we inves
20 reat infantile spasms and refractory complex partial seizures and is in clinical trials to treat addi
21 ly generalized seizures, followed by complex partial seizures and lastly simple partial seizures.
25 Individual analyses of the 30 patients with partial seizures and normal optimal MRI identified a sig
26 st recently presented with continuous simple partial seizures and occasional breakthrough complex par
28 imaging methods for identifying the cause of partial seizures, and can contribute to pre-surgical eva
29 , cingulate, and retrosplenial cortex during partial seizures, and increases in all of these regions
30 al and ictal states in patients with complex partial seizures, and the importance of the transition b
31 n, measured 2 hours after the first stage 2 (partial) seizure, appeared in neurons of the ipsilateral
32 Patients presenting with a history of only partial seizures are at low risk of subsequent tonic-clo
33 f the 10 patients with DNT had postoperative partial seizures arising in the ipsilateral hemisphere,
35 and following seizures that impair (complex partial seizures) but not those that preserve (simple pa
36 onal activity and cerebral metabolism during partial seizures, but found increased neuronal activity
37 ed episodes of epigastric pain), and complex partial seizures consistent with temporal lobe epilepsy.
38 th no impairment of awareness (auras, simple partial seizures) continue, if there is a prior history
39 the frontal cortex during behaviorally mild partial seizures, contrasted with fast polyspike activit
40 sence, generalised tonic-clonic, and complex partial seizures, converge on the same set of anatomical
41 into temporal lobe structures cause complex partial seizures (CPS) and pathological changes observed
43 have also been proposed as models of complex partial seizures (CPSs) following traumatic brain injury
46 ient developed and continues to have complex partial seizures every 2-3 months that are persistent de
47 seizures evoked by pentylenetetrazole (PTZ), partial seizures evoked from the forebrain, absence seiz
48 er presentation), one or more generalised or partial seizures (excluding febrile seizures), a new-ons
49 Secondarily generalized seizures and complex partial seizures exhibited increased slow waves distribu
50 between seizure type (generalized or complex partial), seizure frequency, age of onset and duration o
52 ents who present with only simple or complex partial seizures have a poorly documented prognosis.
53 zure types and the rate of generalization of partial seizures, however rapid-eye-movement sleep seems
54 electroencephalography recordings during 63 partial seizures in 26 patients with surgically confirme
56 or seizures in animals, analogous to complex partial seizures in humans, result in a consistent activ
57 s model mild absence seizures and/or complex partial seizures in humans, then an opportunity may exis
60 eizures) but not those that preserve (simple partial seizures) normal consciousness and responsivenes
64 We report the case of a child with migrating partial seizures of infancy secondary to an activating m
67 roencephalograms in 35 patients with complex partial seizures of temporal lobe origin who were seizur
69 ndent bilateral temporal lobe (IBTL) complex partial seizures on the intracranial electroencephalogra
72 seizures and classified as impaired (complex-partial seizures) or unimpaired (simple-partial seizures
73 three different time periods: (i) during the partial seizure phase prior to generalization; (ii) duri
75 tachycardia (VT) in bipolar disorder (BPD), partial seizures (PSZ) and generalized tonic-clonic seiz
78 nts remained seizure free (apart from simple partial seizures [SPS]) at 5 years after surgery, and 47
79 with pharmacologically intractable, complex-partial seizures, surgical excision of the involved temp
82 erent types of chronic recurrent spontaneous partial seizures that worsen in frequency and duration o
83 ologically extended the neural mass model of partial seizures, the Epileptor, by including two neuron
85 ormations of cortical development (MCDs) and partial seizures, to quantify the GABA(A)-central benzod
89 nimal clonic, maximal tonic, or psychomotor (partial) seizures were determined in 16 different inbred
90 d in the same ictal sites as obvious complex partial seizures, were electrographically similar to rat