Samia Ben Sassi
Overview
Explore the profile of Samia Ben Sassi including associated specialties, affiliations and a list of published articles.
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Articles
47
Citations
450
Followers
0
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Recent Articles
11.
Mohamed W, Eltantawi M, Mecheri Y, Zewde Y, Kamel W, Al-Mubarak B, et al.
Lancet Neurol
. 2024 Jan;
23(2):140-141.
PMID: 38267182
No abstract available.
12.
Jeridi C, Rachdi A, Nabli F, Saied Z, Zouari R, Ben Mohamed D, et al.
J Neurogenet
. 2023 Dec;
37(4):124-130.
PMID: 38109176
Autosomal recessive cerebellar ataxias (ARCA) constitute a highly heterogeneous group of progressive neurodegenerative disorders that typically occur prior to adulthood. Despite some clinical resemblance between these disorders, different genes are...
13.
Zouari R, Saeid M, Marzouk M, Rachdi A, Ben Sassi S
Lupus
. 2023 Oct;
32(13):1561-1571.
PMID: 37887528
Systemic lupus erythematosus (SLE) is a common autoimmune disease with various symptoms involving multiple organs. Neuropsychological manifestations are various and generally serious. Leukoencephalopathy is particularly rare but life-threatening in patients...
14.
Ben Sassi S, Amouri R
Lancet Neurol
. 2023 Oct;
22(11):975-976.
PMID: 37863597
No abstract available.
15.
Kamoun F, Laroussi S, Mellouli A, Jallouli O, Feki S, Ben Sassi S, et al.
J Clin Neuromuscul Dis
. 2023 Aug;
25(1):46-50.
PMID: 37611270
We report a 5-year-old boy who presented with progressive weakness in 4 limbs and gait disorders over 7 months. No skin rash was observed on admission. A symmetrical proximodistal weakness...
16.
Luth T, Gabbert C, Koch S, Konig I, Caliebe A, Laabs B, et al.
Mov Disord
. 2023 Jul;
38(10):1837-1849.
PMID: 37482924
Background: A mitochondrial polygenic score (MGS) is composed of genes related to mitochondrial function and found to be associated with Parkinson's disease (PD) risk. Objective: To investigate the impact of...
17.
Ben Mohamed D, Zouari R, Ketata J, Nabli F, Ben Sassi S
Seizure
. 2023 Mar;
106:168.
PMID: 36894398
No abstract available.
18.
Hamid E, Okengo K, Ayele B, Massi D, Ben Sassi S, Tibar H, et al.
Mov Disord
. 2023 Jan;
38(2):178-184.
PMID: 36703239
No abstract available.
19.
Ben Mohamed D, Saied Z, Ben Sassi S, Ben Said M, Nabli F, Achouri A, et al.
Clin Case Rep
. 2022 Dec;
10(12):e6737.
PMID: 36583195
CLCN2-related leukoencephalopathy (CC2L OMIM#: 615651) is a recently identified rare disorder. It is caused by autosomal recessive mutations in the gene and leads to the dysfunction of its encoded CLC-2...
20.
Ben Mohamed D, Zouari R, Ketata J, Nabli F, Blel S, Ben Sassi S
Seizure
. 2022 Nov;
104:12-14.
PMID: 36446232
Introduction: At the beginning of the coronavirus virus (COVID-19) pandemic, the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) was thought to cause mainly respiratory symptoms, largely sparing the brain and...