Detalhe da pesquisa
1.
Short- vs long-term assessment of heart rate variability: Clinical significance in Dravet Syndrome.
Epilepsy Behav
; 146: 109357, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37499580
2.
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset.
Neurol Sci
; 42(11): 4759-4765, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34292449
3.
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature.
Childs Nerv Syst
; 37(5): 1429-1437, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33604716
4.
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons.
Childs Nerv Syst
; 36(10): 2553-2570, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32564157
5.
Status epilepticus in BRAF-related cardio-facio-cutaneous syndrome: Focus on neuroimaging clues to physiopathology.
Epilepsia Open
; 9(1): 258-267, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37943120
6.
Linear Diagnostic Procedure Elicited by Clinical Genetics and Validated by mRNA Analysis in Neuronal Ceroid Lipofuscinosis 7 Associated with a Novel Non-Canonical Splice Site Variant in MFSD8.
Genes (Basel)
; 14(2)2023 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36833170
7.
Visual Function in Children with GNAO1-Related Encephalopathy.
Genes (Basel)
; 14(3)2023 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36980817
8.
Postoperative Epileptic Seizures in Children.
Children (Basel)
; 9(10)2022 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36291401
9.
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship.
J Clin Med
; 11(20)2022 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36294502
10.
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk.
Seizure
; 94: 129-135, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34896816
11.
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes.
Pediatr Neurol
; 132: 45-49, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35636282
12.
KETASER01 protocol: What went right and what went wrong.
Epilepsia Open
; 7(3): 532-540, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35833327
13.
Cortical Visual Impairment in CDKL5 Deficiency Disorder.
Front Neurol
; 12: 805745, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35153983
14.
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy.
Seizure
; 105: 14-16, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36645998
15.
Calcified cephalohematoma as an unusual cause of EEG anomalies: case report.
J Neurosurg Pediatr
; 19(1): 46-50, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27715482
16.
Acneiform eruption induced by ethosuximide.
Eur J Dermatol
; 24(1): 98-9, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24334200