Detalhe da pesquisa
1.
Rapid versus slow withdrawal of antiepileptic monotherapy in two-year seizure-free adults patients with epilepsy (RASLOW) study: A pragmatic multicentre, prospective, randomized, controlled study.
Neurol Sci;
43(8): 5133-5141, 2022 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35648267
2.
Antidepressant effect of vagal nerve stimulation in epilepsy patients: a systematic review.
Neurol Sci;
41(11): 3075-3084, 2020 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32524324
3.
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
Epilepsia;
60(5): e31-e36, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30719712
4.
Hypertension, seizures, and epilepsy: a review on pathophysiology and management.
Neurol Sci;
40(9): 1775-1783, 2019 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31055731
5.
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.
Neurol Sci;
38(4): 563-570, 2017 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28130605
6.
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
7.
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series.
Int J Legal Med;
129(3): 495-504, 2015 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25119684
8.
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Hum Mol Genet;
21(24): 5359-72, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22949513
9.
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Epilepsia;
54(3): 425-36, 2013 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23360469
10.
PRRT2 mutations are the major cause of benign familial infantile seizures.
Hum Mutat;
33(10): 1439-43, 2012 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22623405
11.
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
Epilepsia;
53(2): 308-18, 2012 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22242659
12.
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy.
Epilepsia;
52(5): e40-4, 2011 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21561445
13.
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations.
J Neurol Sci;
424: 117409, 2021 May 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33773408
14.
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy.
Expert Rev Neurother;
20(3): 251-269, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31941393
15.
The impact of genetics on the classification of epilepsy syndromes.
Epilepsia;
50 Suppl 5: 11-4, 2009 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19469839
16.
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.
Neurosci Lett;
436(1): 23-6, 2008 May 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18355961
17.
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
Epilepsy Res;
80(1): 1-8, 2008 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18440780
18.
Variable course of Unverricht-Lundborg disease: Early prognostic factors.
Neurology;
89(16): 1691-1697, 2017 Oct 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28931642
19.
Similar but not identical: clinical implications for molecular studies in monozygotic discordant twins with epilepsy.
Epilepsy Behav;
20(2): 419, 2011 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21236736
20.
An atypical Bickerstaff's brainstem encephalitis with involvement of spinal cord.
Neuroradiol J;
29(5): 396-9, 2016 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27540012