Souilem S - Search Results

1

Simulation of oleuropein structural conformation in vacuum, water and triolein-water systems using molecular dynamics.

Souilem S, Treesuwan W, Kobayashi I, Khalid N, Bouallagui Z, Neves MA, Uemura K, Isoda H, Sayadi S, Nakajima M. Souilem S, et al. Food Res Int. 2016 Oct;88(Pt A):79-90. doi: 10.1016/j.foodres.2016.04.003. Epub 2016 Apr 14. Food Res Int. 2016. PMID: 28847406

2

Ethyl oleate food-grade O/W emulsions loaded with apigenin: Insights to their formulation characteristics and physico-chemical stability.

Abcha I, Souilem S, Neves MA, Wang Z, Nefatti M, Isoda H, Nakajima M. Abcha I, et al. Among authors: souilem s. Food Res Int. 2019 Feb;116:953-962. doi: 10.1016/j.foodres.2018.09.032. Epub 2018 Sep 11. Food Res Int. 2019. PMID: 30717028

3

Spinal muscular atrophy due to double gene conversion event.

Maamouri W, Hammer MB, Bouhlel Y, Souilem S, Khmiri N, Nehdi H, Hentati F, Amouri R. Maamouri W, et al. Among authors: souilem s. Int J Neurosci. 2011 Feb;121(2):107-11. doi: 10.3109/00207454.2010.529209. Epub 2010 Nov 3. Int J Neurosci. 2011. PMID: 21047176

4

A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia.

Souilem S, Chebel S, Mancuso M, Petrozzi L, Siciliano G, FrihAyed M, Hentati F, Amouri R. Souilem S, et al. J Neurol Sci. 2011 Jan 15;300(1-2):187-90. doi: 10.1016/j.jns.2010.08.065. Epub 2010 Sep 29. J Neurol Sci. 2011. PMID: 20884012

5

A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia.

Souilem S, Kefi M, Mancuso M, Nesti C, Hentati F, Amouri R. Souilem S, et al. Diagn Mol Pathol. 2010 Mar;19(1):28-32. doi: 10.1097/PDM.0b013e3181b00f02. Diagn Mol Pathol. 2010. PMID: 20186009

6

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.

Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshima S, Kudoh J, Hentati F, Nishino I. Driss A, et al. Among authors: souilem s. Neurology. 2003 Apr 22;60(8):1341-4. doi: 10.1212/01.wnl.0000065886.82930.c5. Neurology. 2003. PMID: 12707439

7

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.

Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. Driss A, et al. Among authors: souilem s. Neuromuscul Disord. 2000 Jun;10(4-5):240-6. doi: 10.1016/s0960-8966(00)00099-7. Neuromuscul Disord. 2000. PMID: 10838249

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