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1.
First report of Tunisian patients with CDKL5-related encephalopathy.
Epilepsia Open
; 2023 Sep 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-37701975
2.
A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature.
Int J Dev Neurosci
; 83(4): 383-395, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-37204304
3.
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
4.
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
5.
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
6.
Acute Demyelinating Syndromes: A report of child neurology department of Sfax University Hospital.
Mult Scler Relat Disord
; 56: 103291, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34624647
7.
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.
Mol Genet Genomic Med
; 9(11): e1811, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34549899
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