Detalhe da pesquisa
1.
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.
Epilepsia
; 65(3): 779-791, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38088023
2.
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.
Epilepsia
; 64(6): e105-e111, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37021337
3.
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
Epilepsia
; 2022 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307934
4.
Usefulness of a smartphone application for the diagnosis of epilepsy: Validation study in high-income and rural low-income countries.
Epilepsy Behav
; 115: 107680, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33348193
5.
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Brain
; 142(1): 59-69, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30561534
6.
Lack of evidence for Toxocara infection in Italian myelitis patients.
Neurol Sci
; 41(1): 239-241, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31332580
7.
Eyelid myoclonia with absences: Electroclinical features and prognostic factors.
Epilepsia
; 60(6): 1104-1113, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31087661
8.
Complexity of electrocortical activity as potential biomarker in untreated Parkinson's disease.
J Neural Transm (Vienna)
; 126(2): 167-172, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30506462
9.
Knowledge, stigma, and quality of life in epilepsy: Results before and after a community-based epilepsy awareness program in rural Bolivia.
Epilepsy Behav
; 92: 90-97, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30634158
10.
Knowledge, attitudes, and practices towards epilepsy among general practitioners in rural Bolivia: Results before and after a training program on epilepsy.
Epilepsy Behav
; 83: 113-118, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29694941
11.
Knowledge and attitudes towards epilepsy among nonmedical health workers in rural Bolivia: Results after a long-term activity in the Chaco region.
Epilepsy Behav
; 85: 58-63, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29908385
12.
Electroclinical findings of minor motor events during sleep in temporal lobe epilepsy.
Epilepsia
; 58(7): 1261-1267, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28464288
13.
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
Epilepsia
; 56(4): e40-3, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25752200
14.
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
Am J Hum Genet
; 88(5): 566-73, 2011 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21549341
15.
Febrile infection-related epilepsy syndrome (FIRES) in an adult patient: an early neuroradiological finding.
Neurol Sci
; 40(11): 2407-2410, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31093785
16.
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
Epilepsia
; 54(7): 1288-97, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23621105
17.
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study.
Pediatr Neurol
; 141: 58-64, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36773408
18.
Epilepsy-associated stigma in Bolivia: a community-based study among the Guarani population: an International League Against Epilepsy/International Bureau for Epilepsy/World Health Organization Global Campaign Against Epilepsy Regional Project.
Epilepsy Behav
; 25(1): 131-6, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22917806
19.
Video analysis of epileptic-like motor patterns in REM behaviour disorder: a case series.
Neurol Sci
; 38(4): 699-701, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27988810
20.
Phenotypical heterogeneity of morpheic seizures in ring chromosome 20 syndrome: a videopolysomnographic evidence.
Neurol Sci
; 38(5): 925-926, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28181065