Detalhe da pesquisa
1.
Epilepsia partialis continua: A review.
Neurosciences (Riyadh);
29(2): 71-76, 2024 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38740401
2.
Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families.
J Gene Med;
25(10): e3522, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37119015
3.
Treatment of drop attacks: Anti-seizure drug choices of pediatric neurologists in Saudi Arabia.
Neurosciences (Riyadh);
28(3): 170-176, 2023 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37482388
4.
Valproic acid for children below 2 years of age with epilepsy.
Neurosciences (Riyadh);
26(4): 357-365, 2021 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34663708
5.
Treating epilepsy with options other than antiepileptic medications.
Neurosciences (Riyadh);
25(4): 253-261, 2020 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33130805
6.
Treatment of epileptic drop attacks (atonic seizures) not only depends on skills, but also etiology, tolerability, and EEG.
Neurosciences (Riyadh);
28(4): 281-282, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37844950
7.
Treatment of infantile spasms in Saudi Arabia.
Neurosciences (Riyadh);
23(3): 258-261, 2018 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30008006
8.
Change in presurgical diagnostic imaging evaluation affects subsequent pediatric epilepsy surgery outcome.
Epilepsia;
57(1): 32-40, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26715387
9.
Saudi Epilepsy Society consensus on epilepsy management during the COVID-19 Pandemic.
Neurosciences (Riyadh);
25(3): 222-225, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32683406
10.
Public awareness and attitudes toward epilepsy in Saudi Arabia is improving.
Neurosciences (Riyadh);
19(2): 124-6, 2014 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24739409
11.
Giant Axonal Neuropathy: A Case Report of Subclinical Childhood Manifestations.
Cureus;
16(2): e54368, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38500911
12.
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis.
Genes Genomics;
46(4): 475-487, 2024 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38243045
13.
Parkinsonism-dystonia-2: Case-series study from Saudi Arabia.
Ann Clin Transl Neurol;
11(4): 1063-1066, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38389300
14.
Efficacy and tolerability of perampanel in pediatric patients with Dravet syndrome.
Transl Pediatr;
13(4): 584-595, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38715666
15.
Current Concepts in the Management of Sanfilippo Syndrome (MPS III): A Narrative Review.
Cureus;
16(4): e58023, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38738088
16.
Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement.
Seizure;
117: 174-182, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38432081
17.
Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 families.
Gene;
894: 147986, 2024 Feb 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37956964
18.
Efficacy and Safety of Perampanel in Children with Drug-Resistant Focal-Onset Seizures: A Retrospective Review.
Children (Basel);
10(6)2023 Jun 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37371302
19.
A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report.
Front Pediatr;
11: 1288542, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38046674
20.
Insight into Genetic Mutations of SZT2: Is It a Syndrome?
Biomedicines;
11(9)2023 Aug 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37760843