Works matching IS 00139580 AND DT 2012 AND VI 53 AND IP 12
Results: 26
Family studies of individuals with eyelid myoclonia with absences.
- Published in:
- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2141, doi. 10.1111/j.1528-1167.2012.03692.x
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- Publication type:
- Article
Emil Theodor Kocher-Valve surgery for epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2099, doi. 10.1111/j.1528-1167.2012.03663.x
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- Article
Accelerated long-term forgetting in children with idiopathic generalized epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2135, doi. 10.1111/j.1528-1167.2012.03719.x
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- Publication type:
- Article
Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathies.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2067, doi. 10.1111/j.1528-1167.2012.03656.x
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- Article
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2111, doi. 10.1111/j.1528-1167.2012.03649.x
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- Publication type:
- Article
Mortality by clinical characteristics in a tertiary care cohort of adult patients with chronic epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e212, doi. 10.1111/epi.12006
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- Publication type:
- Article
Frontal lobe function and structure in juvenile myoclonic epilepsy: A comprehensive review of neuropsychological and imaging data.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2091, doi. 10.1111/epi.12003
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- Publication type:
- Article
Geographic variation of epilepsy for older Americans: How close to the geographic variation of stroke?
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2186, doi. 10.1111/j.1528-1167.2012.03640.x
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- Publication type:
- Article
Periictal cerebral tissue hypoxemia: A potential marker of SUDEP risk.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e208, doi. 10.1111/j.1528-1167.2012.03707.x
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- Publication type:
- Article
Epilepsy-related mortality is low in children: A 30-year population-based study in Olmsted County, MN.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2164, doi. 10.1111/j.1528-1167.2012.03661.x
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- Publication type:
- Article
Critical determinants of the epilepsy treatment gap: A cross-national analysis in resource-limited settings.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2178, doi. 10.1111/epi.12002
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- Publication type:
- Article
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e204, doi. 10.1111/epi.12007
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- Publication type:
- Article
Instructions for Authors.
- Published in:
- 2012
- Publication type:
- Editorial
Prevalence of neurocysticercosis among people with epilepsy in rural areas of Burkina Faso.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2194, doi. 10.1111/j.1528-1167.2012.03687.x
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- Publication type:
- Article
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2120, doi. 10.1111/j.1528-1167.2012.03718.x
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- Publication type:
- Article
Neurocognitive profiles in children with epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2156, doi. 10.1111/j.1528-1167.2012.03706.x
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- Publication type:
- Article
Association between sociodemographic status and antiepileptic drug prescriptions in children with epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2149, doi. 10.1111/j.1528-1167.2012.03717.x
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- Publication type:
- Article
Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2128, doi. 10.1111/j.1528-1167.2012.03676.x
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- Publication type:
- Article
Alteration of global workspace during loss of consciousness: A study of parietal seizures.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2104, doi. 10.1111/j.1528-1167.2012.03690.x
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- Publication type:
- Article
Association between epilepsy and cysticercosis and toxocariasis: A population-based case-control study in a slum in India.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2203, doi. 10.1111/epi.12005
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- Publication type:
- Article
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e196, doi. 10.1111/epi.12009
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- Publication type:
- Article
The prognosis of idiopathic generalized epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2079, doi. 10.1111/j.1528-1167.2012.03723.x
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- Publication type:
- Article
A homozygous mutation of voltage-gated sodium channel β<sub>I</sub> gene SCN1B in a patient with Dravet syndrome.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e200, doi. 10.1111/epi.12040
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- Publication type:
- Article
Announcements.
- Published in:
- 2012
- Publication type:
- Calendar
Bone mineral density in a population of children and adolescents with cerebral palsy and mental retardation with or without epilepsy.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2172, doi. 10.1111/j.1528-1167.2012.03639.x
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- Publication type:
- Article
Thank you.
- Published in:
- 2012
- By:
- Publication type:
- Editorial