Search Results - "Sassi Samia, Ben"

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    Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism by Lüth, Theresa, Gabbert, Carolin, Koch, Sebastian, König, Inke R, Caliebe, Amke, Laabs, Björn-Hergen, Hentati, Faycel, Sassi, Samia Ben, Amouri, Rim, Spielmann, Malte, Klein, Christine, Grünewald, Anne, Farrer, Matthew J, Trinh, Joanne

    Published in Movement disorders (01-10-2023)
    “…A mitochondrial polygenic score (MGS) is composed of genes related to mitochondrial function and found to be associated with Parkinson's disease (PD) risk. To…”
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    Journal Article
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    Myoclonus status revealing COVID 19 infection by Ben Mohamed, Dina, Zouari, Rania, Ketata, Jihen, Nabli, Fatma, Blel, Samir, Ben Sassi, Samia

    Published in Seizure (London, England) (01-01-2023)
    “…At the beginning of the coronavirus virus (COVID-19) pandemic, the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) was thought to cause mainly…”
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    The Evolution of Genetic Variability at the LRRK2 Locus by Guenther, Dylan T, Follett, Jordan, Amouri, Rim, Sassi, Samia Ben, Hentati, Faycel, Farrer, Matthew J

    Published in Genes (03-07-2024)
    “…Leucine-rich repeat kinase 2 ( ) c.6055G>A (p.G2019S) is a frequent cause of Parkinson's disease (PD), accounting for >30% of Tunisian Arab-Berber patients. is…”
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    Increased T-bet/GATA-3 and ROR-γt /Foxp3 Ratios in Cerebrospinal Fluid as Potential Criteria for Definite Neuro-Behçet’s Disease by Belghith, Meriam, Maghrebi, Olfa, Cherif, Aroua, Bahrini, Khadija, Saied, Zakaria, Belal, Samir, Sassi, Samia Ben, Barbouche, Mohamed-Ridha, Kchaou, Mariem

    Published in Journal of clinical medicine (29-07-2022)
    “…When the central nervous system (CNS) is the primary affected site in an initial attack of Behçet’s disease (BD), the differential diagnosis is particularly…”
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    Challenges of Parkinson's disease GWASs in African people by Sassi, Samia Ben, Amouri, Rim

    Published in Lancet neurology (01-11-2023)
    “…The variant named rs3115534-G, which is in the non-coding region of GBA1 (the gene encoding the lysosomal enzyme glucocerebrosidase), is reported as a new…”
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    B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet's Disease by Maghrebi, Olfa, Belghith, Meriam, Jeridi, Cyrine, Rachdi, Amine, Fatnassi, Fatma Nabli, Saied, Zakaria, Belal, Samir, Ben Sassi, Samia, Barbouche, Mohamed-Ridha

    Published in Cells (Basel, Switzerland) (12-04-2022)
    “…Remitting-RelapsingMultiple Sclerosis (RRMS) and Neuro-Behçet Disease (NBD) are two chronic neuroinflammatory disorders leading to neurological damage. Herein,…”
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    Myasthenia gravis and COVID‐19: A case series and comparison with literature by Saied, Zakaria, Rachdi, Amine, Thamlaoui, Saber, Nabli, Fatma, Jeridi, Cyrine, Baffoun, Nader, Kaddour, Chokri, Belal, Samir, Ben Sassi, Samia

    Published in Acta neurologica Scandinavica (01-09-2021)
    “…Objective To describe presenting symptoms, clinical outcomes, and therapeutic management of concurrent Coronavirus disease 2019 (COVID‐19) infections in…”
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    Diffuse cerebral edema with leukoencephalopathy revealing systemic lupus erythematosus: A case report and review of literature by Zouari, Rania, Saeid, Mohamed Zakaria, Marzouk, Mahmoud, Rachdi, Amine, Ben Sassi, Samia

    Published in Lupus (01-11-2023)
    “…Background: Systemic lupus erythematosus (SLE) is a common autoimmune disease with various symptoms involving multiple organs. Neuropsychological…”
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    Disability progression in multiple sclerosis: a Tunisian prospective cohort study by Hentati, Emna, Ben Sassi, Samia, Nabli, Fatma, Mabrouk, Tarek, Zouari, Mourad, Hentati, Fayçal

    Published in Neurological sciences (01-05-2018)
    “…Data regarding multiple sclerosis (MS) course in North Africans are scarce and mainly retrospective. To prospectively assess disability progression of multiple…”
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    Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study by Nabli, Fatma, Ben Sassi, Samia, Amouri, Rim, Duda, John E., Farrer, Matthew J., Hentati, Fayçal

    Published in Movement disorders (01-02-2015)
    “…Mutations in the leucine‐rich repeat kinase 2 gene (LRRK2) were found to be a significant cause of late‐onset autosomal dominant forms of Parkinson's disease…”
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