Mamouni S - Search Results

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A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability.

Charif M, Roubertie A, Salime S, Mamouni S, Goizet C, Hamel CP, Lenaers G. Charif M, et al. Among authors: mamouni s. Front Genet. 2015 Oct 19;6:311. doi: 10.3389/fgene.2015.00311. eCollection 2015. Front Genet. 2015. PMID: 26539208 Free PMC article.

Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.

Manes G, Mamouni S, Hérald E, Richard AC, Sénéchal A, Aouad K, Bocquet B, Meunier I, Hamel CP. Manes G, et al. Among authors: mamouni s. Mol Vis. 2017 Apr 3;23:198-209. eCollection 2017. Mol Vis. 2017. PMID: 28442884 Free PMC article.

Probability of myopia in children with high refined carbohydrates consumption in France.

Berticat C, Mamouni S, Ciais A, Villain M, Raymond M, Daien V. Berticat C, et al. Among authors: mamouni s. BMC Ophthalmol. 2020 Aug 18;20(1):337. doi: 10.1186/s12886-020-01602-x. BMC Ophthalmol. 2020. PMID: 32811458 Free PMC article.

Acute hepatitis as a manifestation of secondary syphilis: a case report and literature review.

El Mamouni S, Kadiri M, El Barhdadi IB, Borahma M, Chabib FZ, Lagdali N, Berhili C, Ajana FZ. El Mamouni S, et al. Pan Afr Med J. 2024 Jun 5;48:44. doi: 10.11604/pamj.2024.48.44.42785. eCollection 2024. Pan Afr Med J. 2024. PMID: 39280832 Free PMC article. Review.

Development and Optimization of Alpha-Pinene-Loaded Solid Lipid Nanoparticles (SLN) Using Experimental Factorial Design and Dispersion Analysis.

Zielińska A, Ferreira NR, Durazzo A, Lucarini M, Cicero N, Mamouni SE, Silva AM, Nowak I, Santini A, Souto EB. Zielińska A, et al. Among authors: mamouni se. Molecules. 2019 Jul 24;24(15):2683. doi: 10.3390/molecules24152683. Molecules. 2019. PMID: 31344802 Free PMC article.

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