Detalhe da pesquisa
1.
Neuropsychological group rehabilitation on neurobehavioral comorbidities in children with epilepsy.
Epilepsy Behav
; 103(Pt A): 106386, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31645316
2.
Fertility and marital status in adults with childhood onset epilepsy: A population-based cohort study.
Epilepsia
; 60(7): 1438-1444, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31121078
3.
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy.
Epilepsia
; 59(11): 2125-2136, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30255931
4.
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain
; 136(Pt 10): 3140-50, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24014518
5.
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
; 86(5): 707-18, 2010 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-20398883
6.
Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.
Epilepsia
; 54(9): 1577-85, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23808377
7.
Cognitive impairment in preschool children with epilepsy.
Epilepsia
; 52(8): 1499-505, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21569019
8.
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
Brain
; 133(Pt 7): 2136-47, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20522523
9.
Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB gene.
Neurodegener Dis
; 8(6): 515-22, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21757863
10.
[Seizures in newborn infant]. / Vastasyntyneiden kohtausoireet.
Duodecim
; 126(22): 2610-7, 2010.
Artigo
em Fi
| MEDLINE | ID: mdl-21188877
11.
[Video-EEG in epilepsy diagnostics--when and why?]. / Video-EEG epilepsian diagnostiikassa--milloin ja miksi?
Duodecim
; 125(22): 2514-20, 2009.
Artigo
em Fi
| MEDLINE | ID: mdl-20095120
12.
[Update on current care guidelines. The treatment of status epilepticus]. / Pitkittynyt epileptinen kohtaus.
Duodecim
; 125(22): 2469-71, 2009.
Artigo
em Fi
| MEDLINE | ID: mdl-20095118
13.
Atypical Pattern of Frontal EEG Asymmetry for Direct Gaze in Young Children with Autism Spectrum Disorder.
J Autism Dev Disord
; 49(9): 3592-3601, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31124026
14.
An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases.
Eur J Hum Genet
; 16(2): 176-83, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17971835
15.
Visual and Hearing Impairments After Preterm Birth.
Pediatrics
; 142(2)2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30018154
16.
Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patients.
Eur J Hum Genet
; 15(2): 185-93, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17003839
17.
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
Lancet Neurol
; 6(11): 970-80, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17913586
18.
Atypical physiological orienting to direct gaze in low-functioning children with autism spectrum disorder.
Autism Res
; 10(5): 810-820, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28244277
19.
The incidence and risk factors of epilepsy in children born preterm: A nationwide register study.
Epilepsy Res
; 138: 32-38, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29054051
20.
Refractory generalised convulsive status epilepticus : a guide to treatment.
CNS Drugs
; 19(9): 759-68, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16142991