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1.
Treatment of seizures in the neonate: Guidelines and consensus-based recommendations-Special report from the ILAE Task Force on Neonatal Seizures.
Epilepsia;
64(10): 2550-2570, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37655702
2.
Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy.
Epilepsia;
63(10): 2491-2506, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35842919
3.
[Study of a Tunisian population of children with learning disorders]. / Etude d'une population tunisienne d'enfants en difficultés scolaires.
Tunis Med;
91(6): 382-6, 2013 Jun.
Artículo
en Francés
| MEDLINE | ID: mdl-23868035
4.
Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with Developmental and Epileptic Encephalopathy.
Epilepsia Open;
2023 Oct 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-37867425
5.
Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region.
Front Neurol;
14: 1092887, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36970549
6.
Combined in Silico Prediction Methods, Molecular Dynamic Simulation, and Molecular Docking of FOXG1 Missense Mutations: Effect on FoxG1 Structure and Its Interactions with DNA and Bmi-1 Protein.
J Mol Neurosci;
72(8): 1695-1705, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35654936
7.
Global survey on disruption and mitigation of neurological services during COVID-19: the perspective of global international neurological patients and scientific associations.
J Neurol;
269(1): 26-38, 2022 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-34117527
8.
Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression.
Clin Chim Acta;
508: 287-294, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-32445745
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