Detalhe da pesquisa
1.
Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort.
Epilepsia
; 61(2): 249-258, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31957018
2.
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.
Ann Neurol
; 83(6): 1133-1146, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29679388
3.
Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
Ann Neurol
; 81(3): 419-429, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28133863
4.
Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy.
Epilepsy Behav
; 51: 321-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26340046
5.
Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project.
Epilepsia
; 54(8): 1368-75, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23750890
6.
Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project.
Neurology
; 89(1): 22-28, 2017 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28566546