Detalhe da pesquisa
1.
Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria.
Clin Genet
; 93(2): 228-234, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28386946
2.
Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues.
Epilepsy Behav
; 69: 161-169, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28256379
3.
The 'Seal' of Sir Shackleton.
Eur J Nutr
; 59(7): 2823-2824, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32797253
4.
Mitochondrial disorders and epilepsy.
Rev Neurol (Paris)
; 170(5): 375-80, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24810279
5.
Detection of seizure onset in childhood absence epilepsy.
Clin Neurophysiol
; 163: 267-279, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38644110
6.
Interhemispheric coherence of EEG rhythms in children: Maturation and differentiation in corpus callosum dysgenesis.
Neurophysiol Clin
; 54(3): 102981, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703488
7.
Arterial Spin-Labeling Perfusion Imaging in the Early Stage of Sturge-Weber Syndrome.
AJNR Am J Neuroradiol
; 43(10): 1516-1522, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36137664
8.
Impact of COVID-19 on Spanish patients with Dravet syndrome and their caregivers: consequences of lockdown. / Impacto de la COVID-19 en pacientes españoles con síndrome de Dravet y sus cuidadores: consecuencias del confinamiento.
Rev Neurol
; 73(2): 57-65, 2021 07 16.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-34254661
9.
Physician and patient satisfaction with the switch to remote outpatient encounters in epilepsy clinics during the Covid-19 pandemic.
Seizure
; 91: 60-65, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34098318
10.
Electro-clinical features in epileptic children with chromosome 15q duplication syndrome.
Clin Neurophysiol
; 132(5): 1126-1137, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33773177
11.
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
J Med Genet
; 46(3): 183-91, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18930999
12.
Diagnostic evaluation and management of seizures and status epilepticus in children with known epilepsy or new-onset seizures: A retrospective and comparative analysis.
Arch Pediatr
; 27(2): 66-71, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31964545
13.
Long term response to steroid therapy in Rasmussen encephalitis.
Seizure
; 16(6): 485-92, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17408981
14.
Updating Tuberous sclerosis complex care for pediatric neurologists.
Arch Pediatr
; 29(5S): 5S1-5S2, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36585065
15.
[Neonatal epilepsy and inborn errors of metabolism]. / Epilepsies néonatales et erreurs innées du métabolisme.
Arch Pediatr
; 13(3): 284-92, 2006 Mar.
Artigo
em Francês
| MEDLINE | ID: mdl-16343871
16.
Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndrome.
Exp Neurol
; 283(Pt A): 57-72, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27246997
17.
[Recent advances in pathogenic concepts and therapeutic strategies in Rasmussen's encephalitis]. / Avancées actuelles sur les concepts pathogéniques et thérapeutiques de l'encéphalite de Rasmussen.
Rev Neurol (Paris)
; 161(4): 395-405, 2005 Apr.
Artigo
em Francês
| MEDLINE | ID: mdl-15924075
18.
Early detection of multiple retinal hamartomas during the follow-up of an infant diagnosed with tuberous sclerosis: Contribution of B-scan ultrasonography.
J Fr Ophtalmol
; 43(2): e77-e79, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31859000
19.
Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: confirmation of autosomal recessive inheritance?
Am J Med Genet
; 92(2): 117-21, 2000 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-10797435
20.
Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome?
Am J Med Genet
; 83(2): 82-7, 1999 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-10190477