Detalhe da pesquisa
1.
Seronegative acute encephalitis following COVID-19 vaccines: a case series of an overlooked diagnosis with literature review.
Eur J Clin Pharmacol;
79(7): 975-987, 2023 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37231308
2.
External validations of the ABCD2 score in prediction of stroke risk after transient ischemic attack. A Tunisian hospital-based cohort study.
Int J Neurosci;
133(11): 1218-1223, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33059508
3.
Mitochondrial DNA and Alzheimer's disease: a first case-control study of the Tunisian population.
Mol Biol Rep;
49(3): 1687-1700, 2022 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34854014
4.
A Case of Painful Diplopia after COVID-19 Vaccination: Could It Be Tolosa-Hunt Syndrome?
Korean J Fam Med;
44(4): 240-243, 2023 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37491988
5.
Catatonia in patients with dementia: a case report.
Pan Afr Med J;
33: 117, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31489095
6.
Psychiatric disorders in the acoustic neuroma: about a case.
Pan Afr Med J;
33: 80, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31448042
7.
Primary Hyperparathyroidism and Hyperthyroidism in a Patient with Myotonic Dystrophy: A Case Report and Review of the Literature.
Case Rep Endocrinol;
2015: 735868, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26175917
8.
Seizures and movement disorders induced by hyperglycemia without ketosis in elderly.
Iran J Neurol;
13(3): 172-6, 2014 Jul 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25422738
9.
Cerebral Aneurysms: A Rare Feature of Behçet's Disease-A Case Report and Review of the Literature.
Case Rep Neurol Med;
2013: 812158, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23984129
10.
[Atypical presentation of granulomatosis with polyangiitis: about a pediatric observation]. / Présentation atypique d'une granulomatose avec polyangeite: à propos d'une observation pédiatrique.
Pan Afr Med J;
21: 141, 2015.
Artigo
em Francês
| MEDLINE
| ID: mdl-26327978
11.
48XXYY Syndrome in an Adult with Type 2 Diabetes Mellitus, Unilateral Renal Aplasia, and Pigmentary Retinitis.
Case Rep Med;
20102010.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20827436
12.
Maternally inherited Leigh syndrome: T8993G mutation in a Tunisian family.
Pediatr Neurol;
40(6): 437-42, 2009 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19433277