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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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Neuromyelitis optica and concomitant pulmonary tuberculosis: a case report

Journal of medical case reports, 2021-08, Vol.15 (1), p.1-391, Article 391

2021

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B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet's Disease

Cells (Basel, Switzerland), 2022-04, Vol.11 (8), p.1306

2022

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Management strategy in actinomycosis brain abscess

Clinical case reports, 2023-11, Vol.11 (11), p.n/a

2023

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Leucine-Rich Glioma-Inactivated 1 Encephalitis: Broadening the Sphere

Tremor and other hyperkinetic movements (New York, N.Y.), 2019-10, Vol.9, p.1-3

2019

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Neurological manifestations of creatine transporter deficiency: Two case reports

Journal of the neurological sciences, 2023-12, Vol.455, p.121273, Article 121273

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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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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Neurosarcoidosis: Clinical aspects and diagnostic challenges

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

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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Syndrome de CLIPPERS : à propos de 3 cas

Revue neurologique, 2024-04, Vol.180, p.S159-S160

2024

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Myasthenia gravis and COVID‐19: A case series and comparison with literature

Acta neurologica Scandinavica, 2021-09, Vol.144 (3), p.334-340

2021

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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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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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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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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

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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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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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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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Correction to: Excessive buccal saliva in patients with Parkinson’s disease of the French COPARK cohort

Journal of Neural Transmission, 2021-06, Vol.128 (6), p.871-872

2021

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La mélanomatose neuro-méningée : un diagnostic difficile

Revue neurologique, 2022-04, Vol.178, p.S34-S34

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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Utilization Patterns of Amantadine in Parkinson’s Disease Patients Enrolled in the French COPARK Study

Drugs & aging, 2020-03, Vol.37 (3), p.215-223

2020

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

Neuromyelitis optica and concomitant pulmonary tuberculosis: a case report

B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet's Disease

Management strategy in actinomycosis brain abscess

Leucine-Rich Glioma-Inactivated 1 Encephalitis: Broadening the Sphere

Neurological manifestations of creatine transporter deficiency: Two case reports

Atypical anti-MOG syndrome with intracranial hypertension

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

Neurosarcoidosis: Clinical aspects and diagnostic challenges

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

Syndrome de CLIPPERS : à propos de 3 cas

Myasthenia gravis and COVID‐19: A case series and comparison with literature

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

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

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

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

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

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

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

Correction to: Excessive buccal saliva in patients with Parkinson’s disease of the French COPARK cohort

La mélanomatose neuro-méningée : un diagnostic difficile

Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes

Utilization Patterns of Amantadine in Parkinson’s Disease Patients Enrolled in the French COPARK Study

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