Search Results - "Slassi, Ilham"

Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review by AlSharoqi, Isa Ahmed, Aljumah, Mohamed, Bohlega, Saeed, Boz, Cavit, Daif, Abdelkader, El-Koussa, Salam, Inshasi, Jihad, Kurtuncu, Murat, Müller, Thomas, Retief, Chris, Sahraian, Mohammad Ali, Shaygannejad, Vahid, Slassi, Ilham, Taha, Karim, Zakaria, Magd, Sørensen, Per Soelberg

“…The majority of disease-modifying drugs (DMDs) available for the management of active relapsing–remitting multiple sclerosis (RMS) depend on continuous drug…”
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SARS‐CoV2 disease seen through the prism of acutely decompensated chronic kidney disease and ischemic stroke: What lesson we have learned from using prophylaxis therapy of vascular thromboembolism? by Hazim, Asmaa, Aasfara, Jehanne, Slassi, Ilham, Canaud, Bernard, Haoudar, Amal, Naitlhou, Abdelhamid, El Kettani, Chafik

“…Our case underlines the tight management of antithrombotic therapy in the context of acutely decompensated chronic kidney disease, ischemic stroke, and…”
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A Proteomic Approach for the Involvement of the GAPDH in Alzheimer Disease in the Blood of Moroccan FAD Cases by El Kadmiri, Nadia, Cuardos, Raquel, El Moutawakil, Bouchra, Slassi, Ilham, Avila, Jesus, Nadifi, Sellama, Hachem, Ahmed, Soukri, Abdelaziz

“…Several articles have highlighted the potential involvement of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in neurodegeneration by showing a…”
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Benign Myoclonic Epilepsy of Infancy Evolving to Jeavons Syndrome by Moutaouakil, Fettouma, MD, El Otmani, Hicham, MD, Fadel, Hicham, MD, El Moutawakkil, Bouchra, MD, Slassi, Ilham, MD

“…Benign myoclonic epilepsy of infancy is a rare idiopathic generalized epileptic syndrome occurring below the age of 3 years. Although benign outcome is…”
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Biomarkers for Alzheimer Disease: Classical and Novel Candidates’ Review by El Kadmiri, Nadia, Said, Nadia, Slassi, Ilham, El Moutawakil, Bouchra, Nadifi, Sellama

“…•This review summarizes the contribution of classical and novel biomarkers to AD diagnosis.•CSF classical biomarkers and imaging can provide an increased…”
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Is multiple sclerosis more disabling in North African patients? by Slassi, Ilham

“…Ethnic and environmental factors are major determinant of prevalence and severity of Multiple Sclerosis (MS). Data relating to the severity of MS in…”
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Hemodialysis‐related headache: Still a challenge in 2020? Effect of conventional versus online hemodiafiltration from a study in Casablanca, Morocco by Hazim, Asmaa, Adarmouch, Latifa, Eloury, Aida, Aasfara, Jehanne, Asly, Mouna, Slassi, Ilham

“…Hemodialysis‐related headache (HRH) is a well‐known clinical event. It is considered as one of the most commonly reported neurological symptoms among…”
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Deep Brain Stimulation for Dystonia: Experience of a Moroccan University Hospital by El Otmani, Hicham, El Moutawakil, Bouchra, Daghi, Mohamed, Fadili, Omar, Slassi, Ilham, El Azhari, Abdessamad, Essodegui, Fatiha, Barrou, Lahoucine, Rafai, Mohammed Abdoh, Lakhdar, Abdelhakim

“…Deep brain stimulation (DBS) is a well-established procedure that provides long-term symptom control of the third most common movement disorder: dystonia. In…”
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Neuromyelitis Optica Spectrum Disorder : is it different in Morocco ? (P1.2-082) by Bennis, Anas, El Otmani, Hicham, El Moutawakil, Bouchra, Rafai, Mohammed Abdoh, Sennou, Ilham Slassi

“…Abstract only…”
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Genetic Aspects of Myoclonus–Dystonia Syndrome (MDS) by Rachad, Laila, El Kadmiri, Nadia, Slassi, Ilham, El Otmani, Hicham, Nadifi, Sellama

“…Myoclonus–dystonia (M–D) is an autosomal-dominant movement disorder with onset in the first two decades of life. Mutations in the epsilon-sarcoglycan gene…”
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Assessment of GAPDH expression by quantitative real time PCR in blood of Moroccan AD cases by El Kadmiri, Nadia, El Khachibi, Meryam, Slassi, Ilham, El Moutawakil, Bouchra, Nadifi, Sellama, Soukri, Abdelaziz

“…Highlights • Significant difference of mRNA expression level of GAPDH in AD cases. • The direct involvement of GAPDH in amyloid aggregation. • GAPDH undergoes…”
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COVID-19 pandemic and management of patients with chronic neurological conditions in low-middle income countries: the added burden by Hazim, Asmaa, Yacoubi, Houda, Guennouni, Houda, Aasfara, Jehanne, Bennis, Anas, Slassi, Ilham

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Clinical course of neuromyelitis optica spectrum disorder in a moroccan cohort by Bennis, Anas, El Otmani, Hicham, Benkirane, Nada, Harrizi, Ilham, El Moutawakil, Bouchra, Rafai, Mohammed Abdoh, Slassi, Ilham

“…•Neuromyelitis optica spectrum disorder to multiple sclerosis ratio is high, comparable to Asian and African populations.•North African patients seem to share…”
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Prospective validation of the PML risk biomarker L-Selectin and influence of natalizumab extended intervals by Schwab, Nicholas, Schneider-Hohendorf, Tilman, Pignolet, Béatrice, Bucciarelli, Florence, Scandella, Lise, Ciron, Jonathan, Biotti, Damien, Lebrun-Frenay, Christine, Mathey, Guillaume, Clavelou, Pierre, Pelletier, Jean, Ostkamp, Patrick, Meinl, Ingrid, Windhagen, Susanne, Klotz, Luisa, Gross, Catharina C, Meuth, Sven G, Deisenhammer, Florian, Brassat, David, Wiendl, Heinz

“…Low l-selectin (CD62L) on CD4+ T cells after cryopreservation has been introduced in 2013 as a risk biomarker for the development of progressive multifocal…”
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Association Of Parenchymal And Vascular Damage (Mixed Pattern) In Neurobehçet : A Case Series Study (P5.168) by Habtany, Youness, Dany, Fatima, Benkirane, Nada, El Moutawakil, Bouchra, Rafai, Mohamed Abdoh, Slassi, Ilham

“…Abstract only…”
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Socioeconomic status and stroke prevalence in Morocco: results from the Rabat-Casablanca study by Engels, Thomas, Baglione, Quentin, Audibert, Martine, Viallefont, Anne, Mourji, Fouzi, El Alaoui Faris, Mustapha

“…Stroke is a growing public health concern in low- and middle- income countries. Improved knowledge about the association between socioeconomic status and…”
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A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report by Karkar, Adnane, Barakat, Abdelhamid, Bakhchane, Amina, Fettah, Houda, Slassi, Ilham, Dorboz, Imen, Boespflug-Tanguy, Odile, Nadifi, Sellama

“…X-linked adrenoleukodystrophy (X-ALD; OMIM: 300100) is the most common peroxisomal disease caused by mutations in the ATP-binding cassette, sub-family D member…”
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Intractable Hiccups and Vomiting in Neuromyelitis Optica – A Moroccan Case Series (P02.158) by El Otmani, Hicham, Omari, Salwa, Dany, Fatima, El Moutawakil, Bouchra, Rafai, Mohamed Abdoh, Slassi, Ilham

“…Abstract only…”
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Intractable hiccup and vomiting, neuropathic pruritus and tonic spasms in a case of neuromyelitis optica spectrum disorder by El Otmani, Hicham, Dany, Fatima, El Moutawakil, Bouchra, Abdoh-Rafai, Mohammed, Slassi, Ilham

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Evolution of Molecular Diagnosis of Duchenne Muscular Dystrophy by Itto, Afaf Ben, Hamzi, Khalil, Bellayou, Hanane, Itri, Mohammed, Slassi, Ilham, Nadifi, Sellama

“…Duchenne muscular dystrophy (DMD) is the commonest of the muscular dystrophies. The DMD gene (DMD) is the biggest human gene and the most common molecular…”
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