Detalhe da pesquisa
1.
Fenfluramine below the age of 2 years in Dravet syndrome: What about safety and efficacy?
Epilepsia
; 65(2): e7-e13, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38065833
2.
Current challenges in focal epilepsy treatment: An Italian Delphi consensus.
Epilepsy Behav
; 155: 109796, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38643659
3.
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome.
Cereb Cortex
; 33(17): 9709-9717, 2023 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37429835
4.
Gain of function SCN1A disease-causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication.
Epilepsia
; 64(5): 1331-1347, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36636894
5.
Refining of the electroclinical phenotype in familial and sporadic cases of CSNK2B-related Neurodevelopmental Syndrome.
Epilepsy Behav
; 147: 109436, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37717460
6.
Epilepsy in KBG syndrome.
Dev Med Child Neurol
; 65(5): 712-720, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36196002
7.
Survey on the worldwide availability and affordability of antiseizure medications: Report of the ILAE Task Force on Access to Treatment.
Epilepsia
; 63(2): 335-351, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34981508
8.
Unmet needs and perspectives in management of drug resistant focal epilepsy: An Italian study.
Epilepsy Behav
; 137(Pt A): 108950, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36347069
9.
The Enigma of New Daily Persistent Headache: What Solutions for Pediatric Age?
Curr Pain Headache Rep
; 26(2): 165-172, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35064916
10.
Is Cenobamate the Breakthrough We Have Been Wishing for?
Int J Mol Sci
; 22(17)2021 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502246
11.
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study.
Epilepsia
; 61(11): 2405-2414, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32945537
12.
Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene.
Epilepsia
; 61(11): 2474-2485, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33063863
13.
Defining the phenotype of FHF1 developmental and epileptic encephalopathy.
Epilepsia
; 61(7): e71-e78, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32645220
14.
I stay at home with headache. A survey to investigate how the lockdown for COVID-19 impacted on headache in Italian children.
Cephalalgia
; 40(13): 1459-1473, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33146039
15.
Management of epileptic seizures in school-age children: Educational project dedicated to school staff.
Epilepsy Behav
; 105: 106951, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32086151
16.
Impact of COVID-19 pandemic on pediatric patients with epilepsy - The caregiver perspective.
Epilepsy Behav
; 113: 107527, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242768
17.
Health-related quality of life and the burden of prolonged seizures in noninstitutionalized children with epilepsy.
Epilepsy Behav
; 102: 106340, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31733569
18.
Developmental and epileptic encephalopathy due to SZT2 genomic variants: Emerging features of a syndromic condition.
Epilepsy Behav
; 108: 107097, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32402703
19.
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.
Int J Mol Sci
; 21(10)2020 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32443735
20.
POGZ-related epilepsy: Case report and review of the literature.
Am J Med Genet A
; 179(8): 1631-1636, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31136090