Detalhe da pesquisa
1.
Transition in epilepsy - A pilot study with patients in and outside of academic centers.
Epilepsy Behav
; 151: 109624, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38219605
2.
Touch-screen automatisms in the digital age.
Epilepsy Behav
; 151: 109588, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38160576
3.
Evaluating the Current State of Epilepsy Care in the Province of Ontario.
Can J Neurol Sci
; : 1-3, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38425209
4.
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Genet Med
; 25(3): 100344, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36729052
5.
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy.
Ann Neurol
; 2022 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36534060
6.
Clinical presentation and evaluation of epilepsy with eyelid myoclonia: Results of an international expert consensus panel.
Epilepsia
; 64(9): 2330-2341, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37329145
7.
Management of epilepsy with eyelid myoclonia: Results of an international expert consensus panel.
Epilepsia
; 64(9): 2342-2350, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37326215
8.
Building the Bridge From Pediatric to Adult Neurological Care.
Can J Neurol Sci
; : 1-3, 2023 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37887175
9.
Adults with tuberous sclerosis complex: A distinct patient population.
Epilepsia
; 63(3): 663-671, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34967000
10.
COVID-19 vaccine in patients with Dravet syndrome: Observations and real-world experiences.
Epilepsia
; 63(7): 1778-1786, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35383912
11.
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.
Genet Med
; 23(2): 363-373, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33144681
12.
Blood oxygen level-dependent (BOLD) response patterns with thalamic deep brain stimulation in patients with medically refractory epilepsy.
Epilepsy Behav
; 122: 108153, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34153639
13.
Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study.
Epilepsy Behav
; 115: 107658, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33341393
14.
Impact of the COVID-19 pandemic on people with epilepsy: Findings from the Brazilian arm of the COV-E study.
Epilepsy Behav
; 123: 108261, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34481281
15.
Global characterization of copy number variants in epilepsy patients from whole genome sequencing.
PLoS Genet
; 14(4): e1007285, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29649218
16.
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures.
Am J Hum Genet
; 101(4): 516-524, 2017 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28942967
17.
Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine.
Epilepsia
; 61(11): 2435-2441, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33084037
18.
Genetics of Epileptic Networks: from Focal to Generalized Genetic Epilepsies.
Curr Neurol Neurosci Rep
; 20(10): 46, 2020 08 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32789700
19.
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy.
Epilepsia
; 60(3): 429-440, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828795
20.
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability.
Epilepsia
; 60(8): 1661-1669, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31273778