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Diffuse cerebral edema with leukoencephalopathy revealing systemic lupus erythematosus: A case report and review of literature

Lupus, 2023-11, Vol.32 (13), p.1561-1571

2023

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Myoclonus status revealing COVID 19 infection

Seizure (London, England), 2023-01, Vol.104, p.12-14

2023

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N°214 - Clinical and electrophysiological markers of seropositive versus seronegative myasthenia gravis: A Tunisian cohort of 75 patients

Clinical neurophysiology, 2023-06, Vol.150, p.e140-e140

2023

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Atypical anti-MOG syndrome with intracranial hypertension

Journal of the neurological sciences, 2023-12, Vol.455, p.121851, Article 121851

2023

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Neurosarcoidosis: Clinical aspects and diagnostic challenges

Journal of the neurological sciences, 2023-12, Vol.455, p.121828, Article 121828

2023

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Fahr syndrome: Clinico-radiological polymorphism of a rare neurological pathology

Journal of the neurological sciences, 2023-12, Vol.455, p.122741, Article 122741

2023

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N°262 – Vitamin B12 deficiency related neuropathy: A clinical and electrophysiological study

Clinical neurophysiology, 2023-06, Vol.150, p.e155-e155

2023

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Mitochondrial leucoencephalopathies: An under-diagnosed form of mitochondrial disease

Journal of the neurological sciences, 2021-10, Vol.429, p.119364, Article 119364

2021

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Peripheral neuropathy due to mitochondrial disorders in pediatric patients

Journal of the neurological sciences, 2021-10, Vol.429, p.119365, Article 119365

2021

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Opsoclonus myoclonus induced by lamotrigine toxicity

Seizure (London, England), 2021-10, Vol.91, p.247-250

2021

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Letter to editor response: Why myoclonus is linked to COVID19 infection, not to anti-COVID 19 vaccine

Seizure (London, England), 2023-03, Vol.106, p.168-168

2023

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Troubles du sommeil dans la maladie de Parkinson : lien avec la sévérité de la maladie et les autres signes non-moteurs

Revue neurologique, 2024-04, Vol.180, p.S20-S21

2024

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Myopathies inflammatoires idiopathiques : apport de la biopsie neuromusculaire

Revue neurologique, 2024-04, Vol.180, p.S121-S121

2024

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Sclérose en plaques à début tardif : facteurs associés à une progression rapide du handicap et intérêt du Multiple Sclerosis Severity Score

Revue neurologique, 2024-04, Vol.180, p.S152-S152

2024

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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

Heliyon, 2024-05, Vol.10 (9), p.e30004, Article e30004

2024

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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

Heliyon, 2024-05, Vol.10 (9), p.e30004

2024

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The evolution of cognitive impairment in multiple sclerosis: A longitudinal study

Journal of the neurological sciences, 2021-10, Vol.429, p.118166, Article 118166

2021

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Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105244, Article 105244

2023

Volltextzugriff (PDF)

Factors Associated with Neuropathic Pain in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105246, Article 105246

2023

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Factors Associated with Fatigue in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105245, Article 105245

2023

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Neuromyelitis Optica Spectrum Disorder: Clinical, Radiological Features of Seropositive Patients

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105252, Article 105252

2023

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Une ataxie aiguë révélant une thrombose veineuse cérébrale : à propos de 2 cas

Revue neurologique, 2021-04, Vol.177, p.S88-S89

2021

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Encéphalopathies de Gayet–Wernicke : étude d’une cohorte tunisienne de 20 patients

Revue neurologique, 2022-04, Vol.178, p.S23-S24

2022

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Les manifestations encéphaliques secondaires à la carence en vitamine B12

Revue neurologique, 2022-04, Vol.178, p.S24-S24

2022

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Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes

Journal of neurogenetics, 2023-10, Vol.37 (4), p.124-130

2023

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Diffuse cerebral edema with leukoencephalopathy revealing systemic lupus erythematosus: A case report and review of literature

Myoclonus status revealing COVID 19 infection

N°214 - Clinical and electrophysiological markers of seropositive versus seronegative myasthenia gravis: A Tunisian cohort of 75 patients

Atypical anti-MOG syndrome with intracranial hypertension

Neurosarcoidosis: Clinical aspects and diagnostic challenges

Fahr syndrome: Clinico-radiological polymorphism of a rare neurological pathology

N°262 – Vitamin B12 deficiency related neuropathy: A clinical and electrophysiological study

Mitochondrial leucoencephalopathies: An under-diagnosed form of mitochondrial disease

Peripheral neuropathy due to mitochondrial disorders in pediatric patients

Opsoclonus myoclonus induced by lamotrigine toxicity

Letter to editor response: Why myoclonus is linked to COVID19 infection, not to anti-COVID 19 vaccine

Troubles du sommeil dans la maladie de Parkinson : lien avec la sévérité de la maladie et les autres signes non-moteurs

Myopathies inflammatoires idiopathiques : apport de la biopsie neuromusculaire

Sclérose en plaques à début tardif : facteurs associés à une progression rapide du handicap et intérêt du Multiple Sclerosis Severity Score

Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren's syndrome: A case based – Review

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

The evolution of cognitive impairment in multiple sclerosis: A longitudinal study

Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Factors Associated with Neuropathic Pain in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Factors Associated with Fatigue in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Neuromyelitis Optica Spectrum Disorder: Clinical, Radiological Features of Seropositive Patients

Une ataxie aiguë révélant une thrombose veineuse cérébrale : à propos de 2 cas

Encéphalopathies de Gayet–Wernicke : étude d’une cohorte tunisienne de 20 patients

Les manifestations encéphaliques secondaires à la carence en vitamine B12

Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes

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