Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case report by Kediha, Mohamed Islam, Tazir, Meriem, Sternberg, Damien, Eymard, Bruno, Alipacha, Lamia

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22. Prodromal or Early Multiple Sclerosis: An Algerian Case-Control Study of Emerging Evidence and Utility by Kediha, Mohamed Islam, Moualek, Dalila, Alipacha, Lamia

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Mild cognitive impairment (MCI): Evolutionary diversities in 40 patients. An Algerian study by Kediha, Mohamed Islam, Mostefaoui, Farida, Pacha, Lamia Ali

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101. Pseudotumor Demyelinating Lesions in Inflammatory Diseases of the Central Nervous System: An Algerian Series by Kediha, Mohamed Islam, Boumali, Soraya, Bensid, Fatma, Pacha, Lamia Ali

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102. When Multiple Sclerosis and Neuro Behcet Disease Meet: What Management to Adopt? by Kediha, Mohamed Islam, Moualek, Dalila, Mostefaoui, Farida, Pacha, Lamia Ali

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Moderate phenotype of a congenital myasthenic syndrome type 19 in an Algerian patient by Kediha, Mohamed Islam, Tazir, Meriem, Sternberg, Damien, Eymard, Bruno, Pacha, Lamia Ali

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123. Rare Association Between Neuromyelitis Optica Spectrum Disorder, Anti-synthetase Syndrome and Systemic Lupus Erythematosus in an Adult Female by Kediha, Mohamed Islam, Mostefaoui, Farida, Salah, Sofiane, Djaafri, Rania, Pacha, Lamia Ali

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167. Efficacy and Safety of Natalizumab: Follow up and Real-life Results of an Algerian Hospital Series by Kediha, Mohamed Islam, Mostefaoui, Farida, Moualek, Dalila, Arnane, Soumeya, Pacha, Lamia Ali

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Myélite à anti-MOG et vaccination anti-Covid : association ? À propos d’un cas by Bouakaz, Imene Fatima, Kediha, Mohamed Islam, Saadi, Abdelkrim, Hamalit, Mahdia, Pacha, Lamia Ali

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Clinical, Evolutionary and Etiological Particularities of Inflammatory Optic Neuropathies: An Algerian Population by Islam, Kediha Mohamed, Dalila, Moualek, Fatma, Bouakaz Imene, Lamia, Ali Pacha

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Intérêt des échanges plasmatiques dans le traitement des pathologies neurologiques auto-immunes : une série algérienne by Bouakaz, Imene Fatima, Kediha, Mohamed Islam, Baghdali, Feriel Yasmine, Chelghoum, Souad, Saadi, Abdelkrim, Pacha, Lamia Ali

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Myélite à anti-MOG et vaccination anti-Covid : association ? À propos d’un cas by Bouakaz, Imene Fatima, Kediha, Mohamed Islam, Saadi, Abdelkrim, Hamalit, Mahdia, Pacha, Lamia Ali

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Leuco-encéphalopathie traitable : nouvelle mutation FOLR1 by Saadi, Abdelkrim, Kediha, Mohamed Islam, Mouhouche, Imad, Sanquier, Sylvia, Moualek, Dalila, Bouderba, Radia, Pacha, Lamia Ali

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Aquaporinopathie et mogopathie révélant un cancer mammaire et gastrique : comorbidités ou syndromes neurologiques paranéoplasiques ? by Nouioua, Sonia, Kediha, Mohamed Islam, Nassima, Hecham, Attal, Nabila, Moualek, Dalila, Tazir, Meriem, Pacha, Lamia Ali

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Confusion mentale liée a une forme rare de microangiopathie cérébrale by Bouakaz, Imene Fatima, Saadi, Abdelkrim, Kediha, Mohamed Islam, Bouderba, Radia, Alipacha, Lamia

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SLA du sujet jeune : une variante clinique ou une variabilité phénotypique ? by Mostefaoui, Farida, Aya, Merbouhi, Kediha, Mohamed Islam, Nouioua, Sonia, Alipacha, Lamia

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Paraparésie spastique, épilepsie, retard de développement : mutation homozygote du gène HPDL by Saadi, Abdelkrim, Boyakaz, Imene Fatima, Colleaux, Laurence, Bouderba, Radia, Kediha, Mohamed Islam, Moualek, Dalila, Pacha, Lamia Ali

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Syndromes myasthéniques congénitaux par mutation du gène ColQ : 2 familles, 2 mutations, 2 phénotypes by Kediha, Mohamed Islam, Alipacha, Lamia, Sternberg, Damien, Nouioua, Sonia, Eymard, Bruno, Tazir, Meriem

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Troubles cognitifs dans le Neuro-Behcet : étude cas témoins by Mostefaoui, Farida, Belarbi, Soreya, Kediha, Mohamed Islam, Smail, Nourredine, Tazir, Meriem

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