Search Results - "Nabli, Fatma"

Myoclonus status revealing COVID 19 infection by Ben Mohamed, Dina, Zouari, Rania, Ketata, Jihen, Nabli, Fatma, Blel, Samir, Ben Sassi, Samia

“…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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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study by Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

“…Summary Background Leucine-rich repeat kinase 2 ( LRRK2 ) mutation 6055G→A (Gly2019Ser) accounts for roughly 1% of patients with Parkinson's disease in white…”
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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

“…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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Neuromyelitis optica and concomitant pulmonary tuberculosis: a case report by Saied, Zakaria, Nabli, Fatma, Rachdi, Amine, Jeridi, Cyrine, Douma, Bissene, Belal, Samir, Ben Sassi, Samia

“…Abstract Background Concomitant diagnosis of neuromyelitis optica spectrum disease and pulmonary tuberculosis has rarely been reported. Case report We report a…”
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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

“…Remitting-RelapsingMultiple Sclerosis (RRMS) and Neuro-Behçet Disease (NBD) are two chronic neuroinflammatory disorders leading to neurological damage. Herein,…”
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A Tunisian patient with CLCN2‐related leukoencephalopathy by Ben Mohamed, Dina, Saied, Zacharia, Ben Sassi, Samia, Ben Said, Mariem, Nabli, Fatma, Achouri, Afef, Jeridi, Cyrine, Masmoudi, Saber, Amouri, Rim

“…CLCN2‐related leukoencephalopathy (CC2L OMIM#: 615651) is a recently identified rare disorder. It is caused by autosomal recessive mutations in the CLCN2 gene…”
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Cerebral Venous Thrombosis Presenting With Cerebellar Ataxia and Cortical Blindness by Ben Sassi, Samia, MD, Mizouni, Habiba, MD, Nabli, Fatma, MD, Kallel, Lamia, MD, Kefi, Mounir, MD, Hentati, Fayçal, MD

“…Venous infarction in the cerebellum has been reported only rarely, probably because of the abundant venous collateral drainage in this region. Bilateral…”
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Neurological manifestations of creatine transporter deficiency: Two case reports by Karray, Cyrine, Mohamed, Dina Ben, Rachdi, Amine, Nabli, Fatma, Sassi, Samia Ben

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Fahr syndrome: Clinico-radiological polymorphism of a rare neurological pathology by Hlioui, Loua, Zouari, Rania, Ben Mohamed, Dina, Zakaria Saeid, Mohamed, Rachdi, Amine, Nabli, Fatma, Ben Sassi, Samia

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Neurosarcoidosis: Clinical aspects and diagnostic challenges by Othman, Oumayma Ben, Zouari, Rania, Saeid, Mohamed Zakaria, Nabli, Fatma, Mohamed, Dina Ben, Rachdi, Amine, Sassi, Samia Ben

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Atypical anti-MOG syndrome with intracranial hypertension by Kacem, Donia Hadj, Zouari, Rania, Saeid, Mohamed Zakaria, Mohamed, Dina Ben, Nabli, Fatma, Rachdi, Amine, Sassi, Samia Ben

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Spinal cord ischemia in beta thalassemia major by Mammou, Syrine Ben, Dkhil, Insaf, Gossa, Nayssen, Hammami, Nadia, Nagi, Sonia, Mohamed, Dina Ben, Nabli, Fatma, Sassi, Samia Ben

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N°262 – Vitamin B12 deficiency related neuropathy: A clinical and electrophysiological study by Hlioui, Loua, Zouari, Rania, Ben Mohamed, Dina, Saied, Mohamed Zakaria, Rachdi, Amine, Nabli, Fatma, Ben Sassi, Samia

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Atypical anti-NMDA receptor encephalitis associated with varicella zoster virus infection by Fatma, Nabli, Zakaria, Saied, Mourad, Zouari, Samir, Belal, Samia, Ben Sassi

“…The triggering effect of herpes simplex virus infection on the development of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is now well established…”
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Efficacy of fingolimod in the 2nd line treatment of active relapsing-remitting multiple sclerosis: About a Tunisian cohort of 50 patients by Saied, Zakaria, Ghachem, Ichrak, Nabli, Fatma, Rachdi, Emine, Jeridi, Cyrine, Blel, Samir, Sassi, Samia Ben

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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

“…Objective To describe presenting symptoms, clinical outcomes, and therapeutic management of concurrent Coronavirus disease 2019 (COVID‐19) infections in…”
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Letter to editor response: Why myoclonus is linked to COVID19 infection, not to anti-COVID 19 vaccine by Mohamed, Dina Ben, Zouari, Rania, Ketata, Jihen, Nabli, Fatma, Sassi, Samia Ben

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Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren's syndrome: A case based – Review by Saied, Zakaria, Zouari, Rania, Rachdi, Amine, Nabli, Fatma, Ben Mohamed, Dina, Ben Sassi, Samia

“…Primary Sjogren's syndrome (pSS) is an autoimmune exocrinopathy in which extraglandular signs of pSS are determinant for the prognosis. Involvement of both…”
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Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren's syndrome: A case based – ReviewRemarks concerning care the checklist by Zakaria Saied, Rania Zouari, Amine Rachdi, Fatma Nabli, Dina Ben Mohamed, Samia Ben Sassi

“…Abstract Page: Background: Primary Sjogren's syndrome (pSS) is an autoimmune exocrinopathy in which extraglandular signs of pSS are determinant for the…”
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A comparative study of the clinical and electrophysiological features between Friedreich ataxia and Ataxia with isolated vitamin E deficiency in Tunisia (P1.064) by Jridi, Cyrine, Kharrat, Haifa, Bensassi, Samia, Nabli, Fatma, Blel, Samir, Hentati, Faycal

“…Abstract only…”
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