Works matching IS 00139580 AND DT 2010 AND VI 51 AND IP 9
Results: 44
Genetic risk perception and reproductive decision making among people with epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1874, doi. 10.1111/j.1528-1167.2009.02507.x
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- Publication type:
- Article
Extrafocal threshold reductions in amygdala-kindled rats.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1729, doi. 10.1111/j.1528-1167.2010.02524.x
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- Article
Clinical features of seizures associated with parahippocampal/inferior temporal lesions compared to those with hippocampal sclerosis.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1906, doi. 10.1111/j.1528-1167.2010.02537.x
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- Article
Region-specific changes in gene expression in rat brain after chronic treatment with levetiracetam or phenytoin.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1714, doi. 10.1111/j.1528-1167.2010.02545.x
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- Article
Evaluation of the innate and adaptive immunity in type I and type II focal cortical dysplasias.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1763, doi. 10.1111/j.1528-1167.2010.02547.x
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- Article
Susceptibility of brainstem to kindling and transfer to the forebrain.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1736, doi. 10.1111/j.1528-1167.2010.02551.x
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- Article
Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1870, doi. 10.1111/j.1528-1167.2010.02555.x
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- Article
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1865, doi. 10.1111/j.1528-1167.2010.02558.x
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- Article
Frameshift mutations of the ARX gene in familial Ohtahara syndrome.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1679, doi. 10.1111/j.1528-1167.2010.02559.x
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- Publication type:
- Article
Alteration of NMDA receptor–mediated synaptic interactions in the lateral amygdala associated with seizure activity in a mouse model of chronic temporal lobe epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1754, doi. 10.1111/j.1528-1167.2010.02561.x
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- Article
Alteration of dopamine D2/D3 receptor binding in patients with juvenile myoclonic epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1699, doi. 10.1111/j.1528-1167.2010.02569.x
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- Article
How common is brain atrophy in patients with medial temporal lobe epilepsy?
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1774, doi. 10.1111/j.1528-1167.2010.02576.x
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- Publication type:
- Article
Increased frequency of arousal parasomnias in families with nocturnal frontal lobe epilepsy: A common mechanism?
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1852, doi. 10.1111/j.1528-1167.2010.02581.x
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- Publication type:
- Article
Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1878, doi. 10.1111/j.1528-1167.2010.02587.x
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- Article
Predisposition to epilepsy—Does the ABCB1 gene play a role?
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1882, doi. 10.1111/j.1528-1167.2010.02588.x
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- Article
Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1707, doi. 10.1111/j.1528-1167.2010.02592.x
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- Publication type:
- Article
Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1886, doi. 10.1111/j.1528-1167.2010.02600.x
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- Article
Sodium channel SCN1A and epilepsy: Mutations and mechanisms.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1650, doi. 10.1111/j.1528-1167.2010.02640.x
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- Article
Autoantibodies to glutamic acid decarboxylase in patients with epilepsy are associated with low cortical GABA levels.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1898, doi. 10.1111/j.1528-1167.2010.02644.x
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- Article
Magnetoencephalographic correlates of different types of aura in temporal lobe epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1846, doi. 10.1111/j.1528-1167.2010.02655.x
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- Article
Screening of GABRB3 in French-Canadian families with idiopathic generalized epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1894, doi. 10.1111/j.1528-1167.2010.02642.x
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- Publication type:
- Article
BOLD signal changes preceding negative responses in EEG-fMRI in patients with focal epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1837, doi. 10.1111/j.1528-1167.2010.02643.x
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- Article
Role of cortical dysplasia in epileptogenesis following prolonged febrile seizure.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1809, doi. 10.1111/j.1528-1167.2010.02676.x
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- Publication type:
- Article
Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na<sub>v</sub>1.1.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1669, doi. 10.1111/j.1528-1167.2010.02645.x
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- Article
Familial form of typical childhood absence epilepsy in a consanguineous context.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1889, doi. 10.1111/j.1528-1167.2010.02649.x
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- Publication type:
- Article
The EpiNet project—Invitation to participate in investigator-led clinical research.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1919, doi. 10.1111/j.1528-1167.2010.02647.x
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- Publication type:
- Article
Therapeutic time window of low-frequency stimulation at entorhinal cortex for amygdaloid-kindling seizures in rats.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1861, doi. 10.1111/j.1528-1167.2010.02663.x
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- Publication type:
- Article
Imaging of P-glycoprotein–mediated pharmacoresistance in the hippocampus: Proof-of-concept in a chronic rat model of temporal lobe epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1780, doi. 10.1111/j.1528-1167.2010.02671.x
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- Article
Inhibitory RNA in epilepsy: Research tools and therapeutic perspectives.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1659, doi. 10.1111/j.1528-1167.2010.02672.x
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- Publication type:
- Article
Ketogenic diet exhibits neuroprotective effects in hippocampus but fails to prevent epileptogenesis in the lithium-pilocarpine model of mesial temporal lobe epilepsy in adult rats.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1829, doi. 10.1111/j.1528-1167.2010.02667.x
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- Publication type:
- Article
Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1910, doi. 10.1111/j.1528-1167.2010.02680.x
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- Article
Evaluation of depression risk in LGI1 mutation carriers.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1685, doi. 10.1111/j.1528-1167.2010.02677.x
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- Publication type:
- Article
Induction of sodium channel Na<sub>x</sub> ( SCN7A) expression in rat and human hippocampus in temporal lobe epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1791, doi. 10.1111/j.1528-1167.2010.02678.x
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- Article
Low frequency stimulation decreases seizure activity in a mutation model of epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1745, doi. 10.1111/j.1528-1167.2010.02679.x
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- Publication type:
- Article
Reliability of patterns of hippocampal sclerosis as predictors of postsurgical outcome.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1801, doi. 10.1111/j.1528-1167.2010.02681.x
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- Publication type:
- Article
Continuous local intrahippocampal delivery of adenosine reduces seizure frequency in rats with spontaneous seizures.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1721, doi. 10.1111/j.1528-1167.2010.02700.x
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- Article
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1691, doi. 10.1111/j.1528-1167.2010.02692.x
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- Publication type:
- Article
Utility of 3-T FLAIR and 3D short tau inversion recovery MR imaging in the preoperative diagnosis of hippocampal sclerosis: Direct comparison with 1.5-T FLAIR MR imaging.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1820, doi. 10.1111/j.1528-1167.2010.02685.x
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- Publication type:
- Article
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1902, doi. 10.1111/j.1528-1167.2010.02694.x
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- Publication type:
- Article
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1915, doi. 10.1111/j.1528-1167.2010.02691.x
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- Publication type:
- Article
Announcements.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1920, doi. 10.1111/j.1528-1167.2010.02743.x
- Publication type:
- Article
Erratum.
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- 2010
- Publication type:
- Correction Notice
From the Editors.
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- 2010
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- Publication type:
- Editorial
Instructions for Authors.
- Published in:
- 2010
- Publication type:
- Other