Detalhe da pesquisa
1.
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.
Epilepsia
; 64 Suppl 1: S9-S13, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36994678
2.
Perampanel as adjuvant treatment in epileptic encephalopathies: A multicenter study in routine clinical practice.
Epilepsy Behav
; 134: 108836, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35870432
3.
Clinical outcomes of eslicarbazepine acetate monotherapy for focal-onset seizures: A multicenter audit.
Acta Neurol Scand
; 140(6): 422-428, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31498422
4.
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Brain
; 140(9): 2337-2354, 2017 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29050392
5.
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.
Am J Hum Genet
; 93(5): 967-75, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24207121
6.
[The importance of amygdala removal in the surgical treatment of mesial temporal lobe epilepsy]. / La importancia de la resección amigdalar en el tratamiento quirúrgico de la epilepsia temporal mesial.
Neurocirugia (Astur)
; 26(6): 296-301, 2015.
Artigo
em Espanhol
| MEDLINE | ID: mdl-26188354
7.
Hyperexcitability and epileptic seizures in a model of frontotemporal dementia.
Neurobiol Dis
; 58: 200-8, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23774255
8.
Early Treatment with Metformin Improves Neurological Outcomes in Lafora Disease.
Neurotherapeutics
; 20(1): 230-244, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36303102
9.
Proposed Recommendations for the Management of Depression in Adults with Epilepsy: An Expert Consensus.
Neurol Ther
; 12(2): 479-503, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36692706
10.
Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES).
Clin Neurophysiol
; 131(5): 1030-1039, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32197126
11.
Efficacy and tolerability of zonisamide in idiopathic generalized epilepsy.
Epileptic Disord
; 11(1): 61-6, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19264587
12.
External trigeminal nerve stimulation: A long term follow up study.
Seizure
; 69: 218-220, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31108410
13.
Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features.
Epilepsy Res
; 154: 39-41, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31035243
14.
A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.
Mov Disord
; 27(14): 1826-7, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23225201
15.
Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes.
PLoS One
; 12(11): e0188978, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29190809
16.
Pitfalls in genetic testing: the story of missed SCN1A mutations.
Mol Genet Genomic Med
; 4(4): 457-64, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27465585
17.
Long-term efficacy and safety of lacosamide monotherapy in the treatment of partial-onset seizures: A multicenter evaluation.
Seizure
; 29: 119-22, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26076854
18.
Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1.
Neuromuscul Disord
; 25(3): 222-4, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25578555
19.
Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene.
Epilepsy Res
; 108(8): 1274-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25060993
20.
Jeavons syndrome as an occipital cortex initiated generalized epilepsy: Further evidence from a patient with a photic-induced occipital seizure.
Seizure
; 32: 72-4, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26552567