100 results on '"Essid, M."'
Search Results
2. Photocatalytic degradation of a pharmaceutical pollutant (Levofloxacin) by two-hybrid photocatalysts g-C3N4/TiO2 and WO3/TiO2: comparative study
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Trifi, B., primary, Nahdi, A., additional, Othmani, A., additional, Aloui, Z., additional, Essid, M., additional, and Dhaouadi, H., additional
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- 2023
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3. P412 Expanding the clinical and genetic spectrum of biallelic pathogenic MYO18B variants in congenital myopathy
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Donkervoort, S., primary, Zaharieva, I., additional, Essid, M., additional, Longman, C., additional, Foley, A., additional, Horrocks, I., additional, Benrhouma, H., additional, Farrugia, M., additional, Neuhaus, S., additional, Younes, T., additional, Youssef-Turki, I., additional, Jamshidi, Y., additional, Chao, K., additional, Houlden, H., additional, Maroofian, R., additional, Bönnemann, C., additional, Muntoni, F., additional, and Sarkozy, A., additional
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- 2023
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4. Synthesis, crystal structure, vibrational and optical properties of a new Bi(III) halide complex: (C9H13N2O2)2Bi2Cl8
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Ounally, C., Essid, M., Bruno, G., Abid, S., Faggio, G., and Aloui, Z.
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- 2019
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5. Photocatalytic degradation of a pharmaceutical pollutant (Levofloxacin) by two-hybrid photocatalysts g-C3N4/TiO2 and WO3/TiO2: comparative study.
- Author
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Trifi, B., Nahdi, A., Othmani, A., Aloui, Z., Essid, M., and Dhaouadi, H.
- Abstract
The present paper reports the photodegradation of a pharmaceutical pollutant, Levofloxacin, in an aqueous solution using two photocatalyst nanocomposites, g-C
3 N4 /TiO2 and WO3 /TiO2 , under the influence of solar light and UV irradiation. These as-designed nano-heterostructures were synthesized using the hydrothermal method without organic templates or additives. The characterization results revealed that the used preparation method grants the purity of the prepared composites and gives a nanoscale character product. The effects of the weight ratio of g-C3 N4 /TiO2 and WO3 /TiO2 , the mass of the catalyst and the initial concentration of Levofloxacin on the photocatalytic activity were evaluated under UV light. Results showed that 5 mg/L of Levofloxacin with 20 mg of the prepared nanocomposite with a 5% weight ratio of g-C3 N4 and WO3 allowed a quasi-total degradation of the pharmaceutical pollutant within only 30 min. The photocatalytic activities investigation of the prepared nanocomposites under sunlight irradiation showed that after 50 min of treatment, 66% of degradation is reached with WO3 /TiO2 against 100% with g-C3 N4 /TiO2 . The possible photocatalytic mechanism was thoroughly investigated, explaining the improved photocatalytic activity. This work demonstrates that the prepared nanocomposites' photocatalytic degradation of pharmaceutical pollutants is efficient, providing a friendly environmental strategy. [ABSTRACT FROM AUTHOR]- Published
- 2024
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6. Synthesis and Physico-Chemical Studies of a New Noncentrosymmetric Bis[N-(2-hydroxyethyl)piperazine-1,4-diium] Tetrakis(hydrogen oxalate) Trihydrate: [C6H16N2O]2(HC2O4)4·3H2O
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Essid, M., Rzaigui, M., and Marouani, H.
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- 2015
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7. Synthesis, Hirshfeld surface analysis and physicochemical studies of non-centrosymmetric semi-organic compound: [C10H15N2](H2PO4)
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Essid, M., primary and Aloui, Z., additional
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- 2019
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8. Photorefractive waveguides produced by ion-implantation of fused silica
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Verhaegen, M., primary, Allard, L.B., additional, Brebner, J.L., additional, Essid, M., additional, Roorda, S., additional, and Albert, J., additional
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- 1996
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9. Facteurs prédictifs de survie et de récidive au cours de l’hépatite auto-immune : à propos d’une série tunisienne monocentrique
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Ben Jeddi, H., primary, Kchir, H., additional, Dhouha, C., additional, Dhilel, I., additional, Dabbebi, H., additional, Essid, M., additional, Zargouni, H., additional, and Maamouri, N., additional
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- 2018
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10. Signification pronostique du rapport préopératoire neutrophiles-lymphocytes dans le carcinome rénal non métastatique
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Chaker, K., primary, Sellami, A., additional, Essid, M., additional, Ben Chehida, M., additional, Ben Rhouma, S., additional, and Nouira, Y., additional
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- 2018
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11. Diagnostic et prise en charge du kyste hydatique du rein ouvert dans les voies urinaires
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Chaker, K., primary, Sellami, A., additional, Ouanes, Y., additional, Essid, M., additional, Ben Chehida, M., additional, Ben Rhouma, S., additional, and Nouira, Y., additional
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- 2018
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12. Identification des facteurs déterminants de mortalité de la gangrène gazeuse du périnée
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Chaker, K., primary, Sellami, A., additional, Ouanes, Y., additional, Ben Chehida, M., additional, Essid, M., additional, Abid, K., additional, Ben Rhouma, S., additional, and Nouira, Y., additional
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- 2018
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13. Surrénalectomie pour phéochromocytome : étude comparative entre la voie laparoscopique et voie ouverte
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Saadi, A., primary, Bouzouita, A., additional, Essid, M., additional, Gharbi, M., additional, Ayed, H., additional, Kerkeni, W., additional, Cherif, M., additional, Slama, R. Ben, additional, Derouiche, A., additional, and Chebil, M., additional
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- 2017
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14. Islamic Economic Thought
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Yassine Essid, M., Samuels, Warren J., editor, and Todd Lowry, S., editor
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- 1987
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15. Crystal structure, vibrational and optical properties of a new Bi(III) halide complex: [C6H16N2]5Bi2Br10(BiBr6)2·2H2O
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Essid, M., primary, Aloui, Z., additional, Ferretti, V., additional, Lefebvre, F., additional, and Nasr, C. Ben, additional
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- 2017
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16. Crystal structure, Hirshfeld surface and spectroscopic studies of the noncentrosymmetric Bi(III) halide complex: [C8H12N]3BiCl6
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Essid, M., primary, Aloui, Z., additional, Ferretti, V., additional, Abid, S., additional, Lefebvre, F., additional, Rzaigui, M., additional, and Nasr, C. Ben, additional
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- 2017
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17. Difference in the behavior of oxygen deficient defects in Ge-doped silica optical fiber preforms...
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Essid, M. and Brebner, J.L.
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ELECTRONS , *IONS - Abstract
Presents a study reporting on the difference in the transformation process of the neutral oxygen monovacancy and the germanium lone pair center (GLPC), into electron trap centers associated with fourfold coordinated ions and Ge-E' centers. Methodology used to conduct the study; Description of the sample used; Findings of the study.
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- 1998
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18. Quels sont les facteurs prédictifs de récidive des sténoses de l’urètre après une première urétrotomie interne ?
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Saadi, A., primary, Kerkeni, W., additional, Essid, M., additional, Ayed, H., additional, Bouzouita, A., additional, Cherif, M., additional, slama, R. Ben, additional, Derouiche, A., additional, and Chebil, M., additional
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- 2016
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19. Manifestations dermatologiques associées au virus de l’hépatite C
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Kchir, H., primary, Dabbebi, H., additional, Mahfoudhi, M., additional, Essid, M., additional, Ben Jeddi, H., additional, Chaabouni, H., additional, Maamouri, N., additional, Ben Abdallah, T., additional, and Ben Mami, N., additional
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- 2015
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20. Une rétinopathie diabétique proliférante inaugurant un diabète gestationnel
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Khaldi, N., primary, Essid, M., additional, Malek, I., additional, Boujemaa, C., additional, Bouguila, H., additional, Nacef, L., additional, and Ayed, S., additional
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- 2008
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21. 589 Étude comparative Avastin® versus triamcinolone dans le traitement de l’œdème maculaire diabétique
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Mokni, I., primary, Moalla, S., additional, Malek, I., additional, Essid, M., additional, Mhenni, A., additional, Bouguila, H., additional, and Ayed, S., additional
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- 2008
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22. Synthesis and Physico-Chemical Studies of a New Noncentrosymmetric Bis[ N-(2-hydroxyethyl)piperazine-1,4-diium] Tetraki s(hydrogen oxalate) Trihydrate: [CHNO](HCO)·3HO.
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Essid, M., Rzaigui, M., and Marouani, H.
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OXALATES ,SINGLE crystals ,CRYSTAL structure ,MOLECULAR structure ,HYDROGEN bonding ,NUCLEAR magnetic resonance spectroscopy ,ULTRAVIOLET-visible spectroscopy - Abstract
The new noncentrosymmetric oxalate with the general formula [CHNO](HCO)·3HO, has been synthesized and single crystals were grown from aqueous solution by slow evaporation technique. Single crystal X-ray diffraction study on grown crystal reveals that they belong to triclinic system with space group P1. The unit cell dimensions are: a = 5.688(2) Å, b = 8.315(2) Å, c = 16.634(3) Å, α = 96.63(2)°, β = 99.81(3)°, γ = 110.01(2)° with V = 715.4(3) Å and Z = 1. The structure has been solved using a direct method and refined to a reliability R factor of 0.052. The structure is built up from anionic chains parallel to the a-axis. These chains are interconnected by the organic cations and water molecules via hydrogen bonds so as to build a three dimensional arrangement. FT-IR spectrum confirms the presence of the functional groups in the synthesized material. The C CP-MAS NMR spectrum is in agreement with the X-ray structure. UV-Vis spectrum indicates that the crystal is transparent in UV and visible region with a lower cutoff wavelength of 212 nm. The DSC curve indicates that the crystal is thermally stable up to 330 K. Graphical Abstract: The molecular structure of bis( N-(2-hydroxyethyl)piperazine-1,4-diium) Tetraki s(hydrogen oxalate) Trihydrate is formed by N-(2-hydroxyethyl)piperazine-1,4-diium cations, oxalate anions and water molecules held together by means of N-H⋯O, C-H⋯O, O-H⋯OW and OW-H⋯OW(O) hydrogen bonds to form three-dimensional network.[Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]
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- 2015
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23. 708 Schwannome isolé palpébral : à propos d’un cas
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Marrakchi Kamoun, S., primary, Azaiez, A., additional, Souissi, K., additional, Khaldi, N., additional, Essid, M., additional, Jeddi, A., additional, Nacef, L., additional, and Ayed, S., additional
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- 2005
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24. 665 Récidive du décollement de rétine après ablation de l’indentation épisclérale
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Boujemaa Bacha, C., primary, Azaiez, A., additional, Souissi, K., additional, Essid, M., additional, Hajlaoui, K., additional, Nacef, L., additional, Bouguila, H., additional, and Ayed, S., additional
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- 2005
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25. Answering Queries in the Presence of XML Keys.
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Essid, M., Boucelma, O., and Bressan, S.
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- 2006
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26. Ion implantation induced photosensitivity in Ge-doped silica: Effect of induced defects on refractive index changes
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Essid, M, primary, Brebner, J.L, additional, Albert, J, additional, and Awazu, K, additional
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- 1998
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27. Photorefractive waveguides produced by ion-implantation of fused silica
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Verhaegen, M., primary, Allard, L.B., additional, Brebner, J.L., additional, Essid, M., additional, Roorda, S., additional, and Albert, J., additional
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- 1995
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28. Ion Implantation Induced Photosensitivity in Silica and Ge-Doped Silica
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Essid, M., primary, Verhaegen, M., additional, Allard, L.B., additional, Brebner, J.L., additional, and Albert, J., additional
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- 1995
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29. Correlation between oxygen-deficient center concentration and KrF excimer laser induced defects in thermally annealed Ge-doped optical fiber preforms
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Essid, M., Albert, J., Brebner, J.L., and Awazu, K.
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- 1999
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30. 46th Medical Maghrebian Congress. November 9-10, 2018. Tunis
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Alami Aroussi, A., Fouad, A., Omrane, A., Razzak, A., Aissa, A., Akkad, A., Amraoui, A., Aouam, A., Arfaoui, A., Belkouchi, A., Ben Chaaben, A., Ben Cheikh, A., Ben Khélifa, A., Ben Mabrouk, A., Benhima, A., Bezza, A., Bezzine, A., Bourrahouat, A., Chaieb, A., Chakib, A., Chetoui, A., Daoudi, A., Ech-Chenbouli, A., Gaaliche, A., Hassani, A., Kassimi, A., Khachane, A., Labidi, A., Lalaoui, A., Masrar, A., Mchachi, A., Nakhli, A., Ouakaa, A., Siati, A., Toumi, A., Zaouali, A., Condé, A. Y., Haggui, A., Belaguid, A., abdelkader jalil el hangouche, Gharbi, A., Mahfoudh, A., Bouzouita, A., Aissaoui, A., Ben Hamouda, A., Hedhli, A., Ammous, A., Bahlous, A., Ben Halima, A., Belhadj, A., Blel, A., Brahem, A., Banasr, A., Meherzi, A., Saadi, A., Sellami, A., Turki, A., Ben Miled, A., Ben Slama, A., Daib, A., Zommiti, A., Chadly, A., Jmaa, A., Mtiraoui, A., Ksentini, A., Methnani, A., Zehani, A., Kessantini, A., Farah, A., Mankai, A., Mellouli, A., Touil, A., Hssine, A., Ben Safta, A., Derouiche, A., Jmal, A., Ferjani, A., Djobbi, A., Dridi, A., Aridhi, A., Bahdoudi, A., Ben Amara, A., Benzarti, A., Ben Slama, A. Y., Oueslati, A., Soltani, A., Chadli, A., Aloui, A., Belghuith Sriha, A., Bouden, A., Laabidi, A., Mensi, A., Sabbek, A., Zribi, A., Green, A., Ben Nasr, A., Azaiez, A., Yeades, A., Belhaj, A., Mediouni, A., Sammoud, A., Slim, A., Amine, B., Chelly, B., Jatik, B., Lmimouni, B., Daouahi, B., Ben Khelifa, B., Louzir, B., Dorra, A., Dhahri, B., Ben Nasrallah, C., Chefchaouni, C., Konzi, C., Loussaief, C., Makni, C., Dziri, C., Bouguerra, C., Kays, C., Zedini, C., Dhouha, C., Mohamed, C., Aichaouia, C., Dhieb, C., Fofana, D., Gargouri, D., Chebil, D., Issaoui, D., Gouiaa, D., Brahim, D., Essid, D., Jarraya, D., Trad, D., Ben Hmida, E., Sboui, E., Ben Brahim, E., Baati, E., Talbi, E., Chaari, E., Hammami, E., Ghazouani, E., Ayari, F., Ben Hariz, F., Bennaoui, F., Chebbi, F., Chigr, F., Guemira, F., Harrar, F., Benmoula, F. Z., Ouali, F. Z., Maoulainine, F. M. R., Bouden, F., Fdhila, F., Améziani, F., Bouhaouala, F., Charfi, F., Chermiti Ben Abdallah, F., Hammemi, F., Jarraya, F., Khanchel, F., Ourda, F., Sellami, F., Trabelsi, F., Yangui, F., Fekih Romdhane, F., Mellouli, F., Nacef Jomli, F., Mghaieth, F., Draiss, G., Elamine, G., Kablouti, G., Touzani, G., Manzeki, G. B., Garali, G., Drissi, G., Besbes, G., Abaza, H., Azzouz, H., Said Latiri, H., Rejeb, H., Ben Ammar, H., Ben Brahim, H., Ben Jeddi, H., Ben Mahjouba, H., Besbes, H., Dabbebi, H., Douik, H., El Haoury, H., Elannaz, H., Elloumi, H., Hachim, H., Iraqi, H., Kalboussi, H., Khadhraoui, H., Khouni, H., Mamad, H., Metjaouel, H., Naoui, H., Zargouni, H., Elmalki, H. O., Feki, H., Haouala, H., Jaafoura, H., Drissa, H., Mizouni, H., Kamoun, H., Ouerda, H., Zaibi, H., Chiha, H., Saibi, H., Skhiri, H., Boussaffa, H., Majed, H., Blibech, H., Daami, H., Harzallah, H., Rkain, H., Ben Massoud, H., Jaziri, H., Ben Said, H., Ayed, H., Harrabi, H., Chaabouni, H., Ladida Debbache, H., Harbi, H., Yacoub, H., Abroug, H., Ghali, H., Kchir, H., Msaad, H., Manai, H., Riahi, H., Bousselmi, H., Limem, H., Aouina, H., Jerraya, H., Ben Ayed, H., Chahed, H., Snéne, H., Lahlou Amine, I., Nouiser, I., Ait Sab, I., Chelly, I., Elboukhani, I., Ghanmi, I., Kallala, I., Kooli, I., Bouasker, I., Fetni, I., Bachouch, I., Bouguecha, I., Chaabani, I., Gazzeh, I., Samaali, I., Youssef, I., Zemni, I., Bachouche, I., Bouannene, I., Kasraoui, I., Laouini, I., Mahjoubi, I., Maoudoud, I., Riahi, I., Selmi, I., Tka, I., Hadj Khalifa, I., Mejri, I., Béjia, I., Bellagha, J., Boubaker, J., Daghfous, J., Dammak, J., Hleli, J., Ben Amar, J., Jedidi, J., Marrakchi, J., Kaoutar, K., Arjouni, K., Ben Helel, K., Benouhoud, K., Rjeb, K., Imene, K., Samoud, K., El Jeri, K., Abid, K., Chaker, K., Bouzghaîa, K., Kamoun, K., Zitouna, K., Oughlani, K., Lassoued, K., Letaif, K., Hakim, K., Cherif Alami, L., Benhmidoune, L., Boumhil, L., Bouzgarrou, L., Dhidah, L., Ifrine, L., Kallel, L., Merzougui, L., Errguig, L., Mouelhi, L., Sahli, L., Maoua, M., Rejeb, M., Ben Rejeb, M., Bouchrik, M., Bouhoula, M., Bourrous, M., Bouskraoui, M., El Belhadji, M., Essakhi, M., Essid, M., Gharbaoui, M., Haboub, M., Iken, M., Krifa, M., Lagrine, M., Leboyer, M., Najimi, M., Rahoui, M., Sabbah, M., Sbihi, M., Zouine, M., Chefchaouni, M. C., Gharbi, M. H., El Fakiri, M. M., Tagajdid, M. R., Shimi, M., Touaibia, M., Jguirim, M., Barsaoui, M., Belghith, M., Ben Jmaa, M., Koubaa, M., Tbini, M., Boughdir, M., Ben Salah, M., Ben Fraj, M., Ben Halima, M., Ben Khalifa, M., Bousleh, M., Limam, M., Mabrouk, M., Mallouli, M., Rebeii, M., Ayari, M., Belhadj, M., Ben Hmida, M., Boughattas, M., Drissa, M., El Ghardallou, M., Fejjeri, M., Hamza, M., Jaidane, M., Jrad, M., Kacem, M., Mersni, M., Mjid, M., Serghini, M., Triki, M., Ben Abbes, M., Boussaid, M., Gharbi, M., Hafi, M., Slama, M., Trigui, M., Taoueb, M., Chakroun, M., Ben Cheikh, M., Chebbi, M., Hadj Taieb, M., Ben Khelil, M., Hammami, M., Khalfallah, M., Ksiaa, M., Mechri, M., Mrad, M., Sboui, M., Bani, M., Hajri, M., Mellouli, M., Allouche, M., Mesrati, M. A., Mseddi, M. A., Amri, M., Bejaoui, M., Bellali, M., Ben Amor, M., Ben Dhieb, M., Ben Moussa, M., Chebil, M., Cherif, M., Fourati, M., Kahloul, M., Khaled, M., Machghoul, M., Mansour, M., Abdesslem, M. M., Ben Chehida, M. A., Chaouch, M. A., Essid, M. A., Meddeb, M. A., Gharbi, M. C., Elleuch, M. H., Loueslati, M. H., Sboui, M. M., Mhiri, M. N., Kilani, M. O., Ben Slama, M. R., Charfi, M. R., Nakhli, M. S., Mourali, M. S., El Asli, M. S., Lamouchi, M. T., Cherti, M., Khadhraoui, M., Bibi, M., Hamdoun, M., Kassis, M., Touzi, M., Ben Khaled, M., Fekih, M., Khemiri, M., Ouederni, M., Hchicha, M., Ben Attia, M., Yahyaoui, M., Ben Azaiez, M., Bousnina, M., Ben Jemaa, M., Ben Yahia, M., Daghfous, M., Haj Slimen, M., Assidi, M., Belhadj, N., Ben Mustapha, N., El Idrissislitine, N., Hikki, N., Kchir, N., Mars, N., Meddeb, N., Ouni, N., Rada, N., Rezg, N., Trabelsi, N., Bouafia, N., Haloui, N., Benfenatki, N., Bergaoui, N., Yomn, N., Maamouri, N., Mehiri, N., Siala, N., Beltaief, N., Aridhi, N., Sidaoui, N., Walid, N., Mechergui, N., Mnif, N., Ben Chekaya, N., Bellil, N., Dhouib, N., Achour, N., Kaabar, N., Mrizak, N., Chaouech, N., Hasni, N., Issaoui, N., Ati, N., Balloumi, N., Haj Salem, N., Ladhari, N., Akif, N., Liani, N., Hajji, N., Trad, N., Elleuch, N., Marzouki, N. E. H., Larbi, N., M Barek, N., Rebai, N., Bibani, N., Ben Salah, N., Belmaachi, O., Elmaalel, O., Jlassi, O., Mihoub, O., Ben Zaid, O., Bouallègue, O., Bousnina, O., Bouyahia, O., El Maalel, O., Fendri, O., Azzabi, O., Borgi, O., Ghdes, O., Ben Rejeb, O., Rachid, R., Abi, R., Bahiri, R., Boulma, R., Elkhayat, R., Habbal, R., Tamouza, R., Jomli, R., Ben Abdallah, R., Smaoui, R., Debbeche, R., Fakhfakh, R., El Kamel, R., Gargouri, R., Jouini, R., Nouira, R., Fessi, R., Bannour, R., Ben Rabeh, R., Kacem, R., Khmakhem, R., Ben Younes, R., Karray, R., Cheikh, R., Ben Malek, R., Ben Slama, R., Kouki, R., Baati, R., Bechraoui, R., Fradi, R., Lahiani, R., Ridha, R., Zainine, R., Kallel, R., Rostom, S., Ben Abdallah, S., Ben Hammamia, S., Benchérifa, S., Benkirane, S., Chatti, S., El Guedri, S., El Oussaoui, S., Elkochri, S., Elmoussaoui, S., Enbili, S., Gara, S., Haouet, S., Khammeri, S., Khefecha, S., Khtrouche, S., Macheghoul, S., Mallouli, S., Rharrit, S., Skouri, S., Helali, S., Boulehmi, S., Abid, S., Naouar, S., Zelfani, S., Ben Amar, S., Ajmi, S., Braiek, S., Yahiaoui, S., Ghezaiel, S., Ben Toumia, S., Thabeti, S., Daboussi, S., Ben Abderahman, S., Rhaiem, S., Ben Rhouma, S., Rekaya, S., Haddad, S., Kammoun, S., Merai, S., Mhamdi, S., Ben Ali, R., Gaaloul, S., Ouali, S., Taleb, S., Zrour, S., Hamdi, S., Zaghdoudi, S., Ammari, S., Ben Abderrahim, S., Karaa, S., Maazaoui, S., Saidani, S., Stambouli, S., Mokadem, S., Boudiche, S., Zaghbib, S., Ayedi, S., Jardek, S., Bouselmi, S., Chtourou, S., Manoubi, S., Bahri, S., Halioui, S., Jrad, S., Mazigh, S., Ouerghi, S., Toujani, S., Fenniche, S., Aboudrar, S., Meriem Amari, S., Karouia, S., Bourgou, S., Halayem, S., Rammeh, S., Yaïch, S., Ben Nasrallah, S., Chouchane, S., Ftini, S., Makni, S., Miri, S., Saadi, S., Manoubi, S. A., Khalfallah, T., Mechergui, T., Dakka, T., Barhoumi, T., M Rad, T. E. B., Ajmi, T., Dorra, T., Ouali, U., Hannachi, W., Ferjaoui, W., Aissi, W., Dahmani, W., Dhouib, W., Koubaa, W., Zhir, W., Gheriani, W., Arfa, W., Dougaz, W., Sahnoun, W., Naija, W., Sami, Y., Bouteraa, Y., Elhamdaoui, Y., Hama, Y., Ouahchi, Y., Guebsi, Y., Nouira, Y., Daly, Y., Mahjoubi, Y., Mejdoub, Y., Mosbahi, Y., Said, Y., Zaimi, Y., Zgueb, Y., Dridi, Y., Mesbahi, Y., Gharbi, Y., Hellal, Y., Hechmi, Z., Zid, Z., Elmouatassim, Z., Ghorbel, Z., Habbadi, Z., Marrakchi, Z., Hidouri, Z., Abbes, Z., Ouhachi, Z., Khessairi, Z., Khlayfia, Z., Mahjoubi, Z., and Moatemri, Z.
31. Poster abstracts of the 18th Pan Arab Cancer Congress. TUNISIA. April 19-21, 2018
- Author
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Aarab, J., Abbess, I., Abdalla, F., Abdelaziz, Z., Abdelfattah, S., Abdelli, I., Abdelmajid, K., Abdelsselem, Z., Abdelwahed, N., Abdessayed, N., Abid, B., Abid, K., Abidi, R., Abudabbous, A., Abujanah, S., Aburwais, A., Acacha, E., Acharfi, N., Affes, N., Aftis, R., Ahalli, I., Aid, M., Aissaoui, D., Alaoui, A., Alaoui, M., Albatran, S., Mamdouh, A., Alkikkli, R., Allam, A., Aloulou, S., Alqawi, O., Alragig, M. A., Alsharksi, A., Amaadour, K. O. L., Amaadour, L., Ameziane, N., Ammari, A., Ammour, H., Amrane, R., Annad, N., Aouati, E., Aouichat, S., Aouragh, S., Arifi, S., Astra, M., Atassi, M., Ati, N., Atoui, K., Atreche, L., Ayachi, S., Ayadi, I., Ayadi, M. A., Ayadi, M., Ayari, J., Ayed, H., Ayed, K., Ayedi, H., Ayedi, I., Azegrar, M., Azzouz, H., Babdalla, F., Bachiri, R., Bachiri, Z., Baghdad, M., Bahloul, R., Bahouli, A., Bahri, M., Baississ, I., Bakkali, H., Balti, M., Baraket, O., Bargaoui, H., Batti, R., Bedioui, A., Begag, R., Behourah, Z., Belaid, I., Belaïd, A., Ben Abdallah, A., Ben Abdallah, I., Ben Ahmed, S., Ben Ahmed, T., Ben Azaiz, M., Ben Chehida, M. A., Ben Fatma, L., Ben Ghachem, D., Ben Ghachem, T., Ben Hassouna, J., Ben Hmida, S., Ben Nasr, S., Ben Nejima, D., Ben Rahal, K., Ben Rejeb, M., Ben Rhouma, S., Ben Safta, I., Ben Salem, A., Ben Zargouna, Y., Benabdallah, I., Benabdella, H., Benabdessalem, M. Z., Benahmed, K., Benahmed, S., Benameur, H., Benasr, S., Benbrahim, F., Benbrahim, W., Benbrahim, Z., Benchehida, M., Bencheikh, Y., Bendhiab, T., Benfatma, L., Bengueddach, A., Benhami, M., Benhassouna, J., Benhbib, W., Benjaafar, N., Benkali, R., Benkridis, W., Benlaloui, A., Benmaitig, M., Benmansour, A., Benmouhoub, M., Benna, F., Benna, H., Benna, M., Bennabdellah, H., Benrahal, K., Bensafta, I., Bensalah, H., Bensalem, A., Bensaud, M., Benslama, R., Benyoub, M., Benzid, K., Bergaoui, H., Beroual, M., Berrad, S., Berrazaga, Y., Bezzaz, Z., Bhiri, H., Bibi, M., Binous, M. Y., Blel, A., Boder, J. M., Bouaouina, N., Bouaziz, H., Bouchoucha, S., Boudawara, T., Boudawara, Z., Bouderbala, A., Bouhali, R., Bouhani, M., Boujarnija, R., Boujelben, S., Boujelbene, N., Boukerzaza, I., Boukhari, H., Boulfoul, W., Boulma, R., Boumansour, N., Bouned, A., Bounedjar, A., Bouraoui, I., Bouraoui, S., Bourigua, R., Bourmech, M., Bousaffa, H., Bousahba, A., Bousrih, C., Boussarsar, A., Boussen, H., Boutayeb, S., Bouzaidi, K., Bouzaiene, F., Bouzaiene, H., Bouzerzour, Z., Bouzid, K., Bouzid, N., Bouzidi, D., Bouzidi, W., Bouzouita, A., Brahimi, S., Brahmia, A., Buhmeida, A., Chaaben, K., Chaabouni, H., Chaabouni, M., Chaabène, K., Chaari, H., Chaari, I., Chaari, M., Chabchoub, I., Chabeene, K., Chaker, K., Chakroun, M., Charfi, M., Charfi, S., Chargui, R., Charles, M., Chebil, M., Cheikchouk, K., Chelly, B., Chelly, I., Cheraiet, N., Cherif, A., Cherif, M., Cherifi, A., Chikhrouhou, T., Chikouche, A., Chirouf, A., Chraiet, N., Collan, Y., Cui, Z., Dabbebi, H., Daldoul, A., Damouche, I., Daoud, H., Daoud, N., Daoued, J., Darif, K., Darwish, D. O., Derbouz, Z., Derouiche, A., Dhibe, T. T., Dhibet, T., Djallaoui, A., Djami, N., Djebbes, K., Djedi, H., Djeghim, S., Djellali, L., Djellaoui, A., Djilat, K., Djouabi, R., Doumbia, H., Drah, M., Dridi, M., Hsairi, M., Elabbassi, S., Elallia, F., Elati, Z., Elattassi, M., Elbenna, H., Elfagieh, M. A., Elfaitori, O., Elfannas, H., Elghali, A., Elghali, M. A., Elgonti, S., Elhadj, O. E., Elhazzaz, R., Elkacemi, H., Elkinany, K., Elkissi, Y., Elloumi, F., Elmaalel, O., Elmajjaou, I. S., Elmajjaoui, S., Elmhabrech, H., Elmrabet, F., Elsaghayer, W. A., Elzagheid, A., Emaetig, F., Erraichi, H., Essid, M., Ewshah, N., Ezzairi, F., Faleh, R., Fallah, S., Farag, A. L., Farhat, L., Fehri, R., Feki, J., Fendri, S., Fessi, Z., Filali, T., Fissah, A., Fourati, M., Fourati, N., Frikha, M., Fuchs, C. S., Gabssi, A., Gachi, F., Gadria, S., Gammoudi, A., Ganzoui, I., Gargoura, A., Ghaddabb, I., Gharbi, I., Gharbi, M., Ghazouani, E., Gheriani, N., Ghorbel, A., Ghorbel, L., Ghozi, A., Ghrissi, R., Gouader, A., Goucha, A., Guebsi, A., Guellil, I., Guermazi, F., Guesmi, S., Guetari, W., Habak, N., Haddad, A., Haddad, S., Haddaoui, A., Hadef, I., Hader, A. F., Hadiji, A., Hadjarab, F., Hadoussa, M., Hadoussa, N., Hafsa, C., Hafsia, M., Hajji, A., Hajmansour, M., Hamdi, S., Hamici, Z., Hamida, S., Hamila, F., Hamissa, S., Hammouda, B., Haouet, S., Harhira, I., Haroun, A., Hassouni, K., Hdiji, A., Hechiche, M., Hejjane, L., Hellal, C., Henni, M., Herbegue, K., Hichami, L., Hikem, M., Hmad, A., Hmida, L., Hmissa, S., Hochlaf, M., Houas, A., Houhani, M., Huwidi, A., Ian, C., Ibrahim, B. N., Ibrahim, N. Y., Idir, H., Issaoui, D., Itaimi, A., Izem, A. E., Jaidane, O., Jamel, D., Jamous, H., Jarrar, M., Jarrar, M. S., Jarray, S., Jebsi, M., Jmal, H., Juwid, A., Kaabia, O., Kablouti, A., Kacem, I., Kacem, K., Kaid, M. Y., Kallel, M., Kallel, R., Kammoun, H., Kari, S., Karrit, S., Kchir, H., Kchir, N., Kebdani, T., Kechad, N., Kehili, H., Kerboua, E., Keskes, H., Kessi, N. N., Khababa, N., Khaldi, H., Khanfir, A., Khater, B., Khelif, A., Khemiri, S., Khennouf, K., Khouni, H., Khrouf, S., Kmira, Z., Kochbati, L., Korbi, A., Kouadri, N., Kouhen, F., Krarti, M., Handoussa, M., Hsu, Y., Laakom, O., Laato, M., Labidi, S., Lahlali, F., Lahmidi, A., Lalaoui, A., Lamia, N., Lamri, A., Letaief, F., Letaief, M. R., Aldehmani, M., Rafael, A., Liepa, A. M., Limaiem, F., Limam, K., Loughlimi, H., Ltaief, F., Maamouri, N., Mabrouk, M., Madouri, R., Mahjoub, N., Mahjoubi, Z., Mahrsi, M., Makrem, H., Mallek, W., Manitta, M., Mansoura, L., Mansouri, H., Maoua, M., Maoui, W., Marouene, C., Marzouk, K., Masmoudi, S., May, F., Meddeb, I., Meddeb, K., Meddour, S., Medhioub, F., Mejri, N., Melizi, M. R., Mellas, N., Melliti, R., Melzi, A., Merair, N., Merrouki, F. Z., Mersali, C., Messalbi, O., Messaoudi, L., Messioud, S., Messoudi, K., Mestiri, S., Mezlini, A., Mghirbi, F., Mhabrech, H., Mhiri, A., Midoun, N., Milud, R., Missaoui, B., Mnasser, A., Mnejja, W., Mokni, M., Mokrani, A., Mokrani, M., Moujahed, R., Moukasse, Y., Mouzount, A., Mrad, K., Mraidha, M. H., Mrizak, N., Mzali, R., Mzid, Y., M Ghirbi, F., Nakhli, A., Nasr, C., Nasri, S., Noubigh, G., Nouha, D., Nouia, L., Nouira, Y., Noureddine, A., Nouri, O., Ohtsu, A., Ouahbi, H., Oualla, K., Ouanes, Y., Ouaz, H., Ouikene, A., Ouldbessi, N., Parker, I., Pyrhonen, S., Rachdi, H., Rahal, K., Rahoui, M., Raies, H., Rameh, S., Reguieg, K., Rejab, H., Rejiba, R., Rhim, M. S., Riahi, S., Rouimel, N., Saad Saoud, N., Saadi, K., Saadi, M., Sadou, A., Saguem, I., Sahnoun, T., Sahnoune, H., Sakhri, S., Sallemi, A., Sassi, A., Sbika, W., Sedkaoui, C., Sefiane, S., Sellami, A., Seppo, P., Sfaoua, H., Sghaier, S., Shagan, A., Siala, W., Slim, I., Slimene, M., Soltani, S., Souilah, S., Souissi, M., Sriha Badreddine, B., Swaisi, Y., Taibi, A., Taktak, T., Talbi, G., Talha, S. W., Talima, S. M., Tbessi, S., Tebani, N., Tebra, S., Tebramrad, S., Telaijia, D., Tenni, A., Tolba, A., Topov, Y., Touil, K., Toumi, N., Toumi, W., Tounsi, N., Trigui, A., Trigui, R., Triki, W., Walha, M., Werda, I., Yacoub, H., Yahyaoui, Y., Yaich, A., Yaici, R., Yamouni, M., Yeddes, I., Yekrou, D., Yousfi, M., Yousfi, N., Youssfi, M. A., Zaabar, L., Zaied, S., Zaim, I., Walid ZAKHAMA, Zayed, S., Zehani, A., Zemni, I., Zenzri, Y., Zeraoula, S., Zouiten, O., Zoukar, O., Zrafi, W., Zribi, A., and Zubia, N.
32. Abstracts of the 40th National Congress of Medicine Tunis, 19-20 October 2017
- Author
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Abdallah, M., Abdelaziz, A., Abdelaziz, O., Abdelhedi, N., Abdelkbir, A., Abdelkefi, M., Abdelmoula, L., Abdennacir, S., Abdennadher, M., Abidi, H., Abir Hakiri, A., Abou El Makarim, S., Abouda, M., Achour, W., Aichaouia, C., Aissa, A., Aissa, Y., Aissi, W., Ajroudi, M., Allouche, E., Aloui, H., Aloui, D., Amdouni, F., Ammar, Y., Ammara, Y., Ammari, S., Ammous, A., Amous, A., Amri, A., Amri, M., Amri, R., Annabi, H., Antit, S., Aouadi, S., Arfaoui, A., Assadi, A., Attia, L., Attia, M., Ayadi, I., Ayadi Dahmane, I., Ayari, A., Azzabi, S., Azzouz, H., B Mefteh, N., B Salah, C., Baccar, H., Bachali, A., Bahlouli, M., Bahri, G., Baïli, H., Bani, M., Bani, W., Bani, M. A., Bassalah, E., Bawandi, R., Bayar, M., Bchir, N., Bechraoui, R., Béji, M., Beji, R., Bel Haj Yahia, D., Belakhel, S., Belfkih, H., Belgacem, O., Belgacem, N., Belhadj, A., Beltaief, N., Ben Abbes, M., Ben Abdelaziz, A., Ben Ahmed, I., Ben Aissia, N., Ben Ali, M., Ben Ammar, H., Ben Ammou, B., Ben Amor, A., Ben Amor, M., Benatta, M., Ben Ayed, N., Ben Ayoub, W., Ben Charrada, N., Ben Cheikh, M., Ben Dahmen, F., Ben Dhia, M., Ben Fadhel, S., Ben Farhat, L., Ben Fredj Ismail, F., Ben Hamida, E., Ben Hamida Nouaili, E., Ben Hammamia, M., Ben Hamouda, A., Ben Hassine, L., Ben Hassouna, A., Ben Hasssen, A., Ben Hlima, M., Ben Kaab, B., Ben Mami, N., Ben Mbarka, F., Ben Mefteh, N., Ben Kahla, N., Ben Mrad, M., Ben Mustapha, N., Ben Nacer, M., Ben Neticha, K., Ben Othmen, E., Ben Rhouma, S., Ben Rhouma, M., Ben Saadi, S., Ben Safta, A., Ben Safta, Z., Ben Salah, C., Ben Salah, N., Ben Sassi, S., Ben Sassi, J., Ben Tekaya, S., Ben Temime, R., Ben Tkhayat, A., Ben Tmim, R., Ben Yahmed, Y., Ben Youssef, S., Ben Atta, M., Ben Salah, M., Berrahal, I., Besbes, G., Bezdah, L., Bezzine, A., Bokal, Z., Borsali, R., Bouasker, I., Boubaker, J., Bouchekoua, M., Bouden, F., Boudiche, S., Boukhris, I., Bouomrani, S., Bouraoui, S., Bourgou, S., Boussabeh, E., Bouzaidi, K., Chaker, K., Chaker, L., Chaker, A., Chaker, F., Chaouech, N., Charfi, M., Charfi, M. R., Charfi, F., Chatti, L., Chebbi, F., Chebbi, W., Cheikh, R., Cheikhrouhou, S., Chekir, J., Chelbi, E., Chelly, I., Chelly, B., Chemakh, M., Chenik, S., Cheour, M., Cherif, E., Cherif, Y., Cherif, W., Cherni, R., Chetoui, A., Chihaoui, M., Chiraz Aichaouia, C., Dabousii, S., Daghfous, A., Daib, A., Daib, N., Damak, R., Daoud, N., Daoud, Z., Daoued, N., Debbabi, H., Demni, W., Denguir, R., Derbel, S., Derbel, B., Dghaies, S., Dhaouadi, S., Dhilel, I., Dimassi, K., Dougaz, A., Dougaz, W., Douik, H., Douik El Gharbi, L., Dziri, C., El Aoud, S., El Hechmi, Z., El Heni, A., Elaoud, S., Elfeleh, E., Ellini, S., Ellouz, F., Elmoez Ben, O., Ennaifer, R., Ennaifer, S., Essid, M., Fadhloun, N., Farhat, M., Fekih, M., Fourati, M., Fteriche, F., G Hali, O., Galai, S., Gara, S., Garali, G., Garbouge, W., Garbouj, W., Ghali, O., Ghali, F., Gharbi, E., Gharbi, R., Ghariani, W., Gharsalli, H., Ghaya Jmii, G., Ghédira, F., Ghédira, A., Ghédira, H., Ghériani, A., Gouta, E. L., Guemira, F., Guermazi, E., Guesmi, A., Hachem, J., Haddad, A., Hakim, K., Hakiri, A., Hamdi, S., Hamed, W., Hamrouni, S., Hamza, M., Haouet, S., Hariz, A., Hendaoui, L., Hfaidh, M., Hriz, H., Hsairi, M., Ichaoui, H., Issaoui, D., Jaafoura, H., Jazi, R., Jazia, R., Jelassi, H., Jerraya, H., Jlassi, H., Jmii, G., Jouini, M., Kâaniche, M., Kacem, M., Kadhraoui, M., Kalai, M., Kallel, K., Kammoun, O., Karoui, M., Karouia, S., Karrou, M., Kchaou, A., Kchaw, R., Kchir, N., Kchir, H., Kechaou, I., Kerrou, M., Khaled, S., Khalfallah, N., Khalfallah, M., Khalfallah, R., Khamassi, K., Kharrat, M., Khelifa, E., Khelil, M., Khelil, A., Khessairi, N., Khezami, M. A., Khouni, H., Kooli, C., Korbsi, B., Koubaa, M. A., Ksantini, R., Ksentini, A., Ksibi, I., Ksibi, J., Kwas, H., Laabidi, A., Labidi, A., Ladhari, N., Lafrem, R., Lahiani, R., Lajmi, M., Lakhal, J., Laribi, M., Lassoued, N., Lassoued, K., Letaif, F., Limaïem, F., Maalej, S., Maamouri, N., Maaoui, R., Maâtallah, H., Maazaoui, S., Maghrebi, H., Mahfoudhi, S., Mahjoubi, Y., Mahjoubi, S., Mahmoud, I., Makhlouf, T., Makni, A., Mamou, S., Mannoubi, S., Maoui, A., Marghli, A., Marrakchi, Z., Marrakchi, J., Marzougui, S., Marzouk, I., Mathlouthi, N., Mbarek, K., Mbarek, M., Meddeb, S., azza mediouni, Mechergui, N., Mejri, I., Menjour, M. B., Messaoudi, Y., Mestiri, T., Methnani, A., Mezghani, I., Meziou, O., Mezlini, A., Mhamdi, S., Mighri, M., Miled, S., Miri, I., Mlayeh, D., Moatemri, Z., Mokaddem, W., Mokni, M., Mouhli, N., Mourali, M. S., Mrabet, A., Mrad, F., Mrouki, M., Msaad, H., Msakni, A., Msolli, S., Mtimet, S., Mzabi, S., Mzoughi, Z., Naffeti, E., Najjar, S., Nakhli, A., Nechi, S., Neffati, E., Neji, H., Nouira, Y., Nouira, R., Omar, S., Ouali, S., Ouannes, Y., Ouarda, F., Ouechtati, W., Ouertani, J., Ouertani, H., Oueslati, A., Oueslati, J., Oueslati, I., Rabai, B., Rahali, H., Rbia, E., Rebai, W., Regaïeg, N., Rejeb, O., Rhaiem, W., Rhimi, H., Riahi, I., Ridha, R., Robbena, L., Rouached, L., Rouis, S., Safer, M., Saffar, K., Sahli, H., Sahraoui, G., Saidane, O., Sakka, D., Salah, H., Sallami, S., Salouage, I., Samet, A., Sammoud, K., Sassi Mahfoudh, A., Sayadi, C., Sayhi, A., Sebri, T., Sedki, Y., Sellami, A., Serghini, M., Sghaier, I., Skouri, W., Slama, I., Slimane, H., Slimani, O., Souhail, O., Souhir, S., Souissi, A., Souissi, R., Taboubi, A., Talbi, G., Tbini, M., Tborbi, A., Tekaya, R., Temessek, H., Thameur, M., Touati, A., Touinsi, H., Tounsi, A., Tounsia, H., Trabelsi, S., Triki, A., Triki, M., Turki, J., Turki, K., Twinsi, H., Walha, Y., Wali, J., Yacoub, H., Yangui, F., Yazidi, M., Youssef, I., Zaier, A., Zainine, R., Zakhama, L., Zalila, H., Zargouni, H., Zehani, A., Zeineb, Z., Zemni, I., Zghal, M., Ziadi, J., Zid, Z., Znagui, I., Zoghlami, C., Zouaoui, C., Zouari, B., Zouiten, L., and Zribi, H.
33. Oral communication and poster abstracts of the 22nd National Congress of Gastroenterology joint to the 4th Maghrebian Congress of Gastroenterology. December 2018
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Bellabah, A., Benkirane, A., Ibrahimi, A., Nakhli, A., Sair, A., Essaid, A., Blel, A., Lahchaichi, A., Ben Slama, A., Ouni, A., Amouri, A., Jemaa, A., Cherif, A., Khsiba, A., Hssine, A., Djobbi, A., Guedich, A., Laabidi, A., Mensi, A., Ouakaa, A., Sriha, A., Choukri, A., Green, A., Belkhamsa, A., Hammami, A., Bourigua, A., Filali, A., Belabeh, A., Sentissi, A., Ait Errami, A., Nadi, A., Filankembo, A., Lamine, A., Badre, W., Ben Kaab, B., Ben Slimane, B., S, B., Hasnaoui, B., Bouchabou, B., Bouguerra, C., Baccouche, C., Ayadi, C., Bennasrallah, C., Benajah, D., Gargouri, D., Zehi, D., Issaoui, D., Cherif, D., Ben Ghachem, D., Trad, D., Bouaiti, E., Boutouria, E., Bel Hadj Mabrouk, E., Chalbi, E., Aait, E., Bouhamou, F., Haddad, F., Lairani, F., Saffar, F., Torjmen, F., Haj Kacem, F., Hamdane, F., Chabib, F. Z., Elrhaoussi, F. Z., Moumayez, F. Z., Loukil, F., Ahmed Djouldé Diallo, F., Aissaoui, F., Ajana, F., Chabib, F., Hamdoun, F., Moumayez, F., Bennani Kella, G., Bennani, G., Abid, H., Cheikhani, H., Ouazzani, H., Romdhane, H., Hassan SEDDIK, Sghir, H., Debbabi, H., Ben Jeddi, H., Garraoui, H., Letaief, H., Kchir, H., Elloumi, H., Hammami, H., Jaziri, H., Ben Abdallah, H., Chaabouni, H., Ben Romdhane, H., Yacoub, H., Gdoura, H., Sahli, H., Loghmari, H., Bouguerra, H., Maghrebi, H., Ben Nejma, H., Jlassi, H., Fourati, H., Alaoui, H., Ismail, H., Benelbarhdadi, I., Cohen, I., Errabih, I., Koti, I., Doghri, I., Elhidaoui, I., Haraki, I., Cheikh, I., Abdelaali, I., Jemni, I., Bouennene, I., Akoch, I., H, I., Boubaker, J., Krati, K., Eljery, K., Temani, K., Bellil, K., Chabbouh, K., Boughoula, K., Ouazzani, L., Ben Yaghlene, L., Kallel, L., A, L., Hamzaoui, L., Chtourou, L., Ben Farhat, L., Bouabid, L., Mnif, L., Mouelhi, L., Safer, L., Zouiten Mekki, L., Bourehma, M., El Akbari, M., El Khayari, M., Elyousfi, M., Firwana, M., Lahlali, M., Tahiri, M., Mestouri, M., Abdelwahed, M., Ben Hamida, M., Ben Chaabane, M., Moalla, M., Yakoubi, M., Sabbah, M., Serghini, M., Amri, M., Ben Abbes, M., Ben Cheikh, M., Ghribi, M., Hafi, M., Ben Abdelwahed, M., Ksiaa, M., Essid, M., Zakhama, M., Yousfi, M., Ayari, M., Belhadj, M., Cheickh, M., Kacem, M., Horma Alaoui, M., Abid, M., Bennour, M. A., Ghanem, M., Loghmari, M. H., Douggui, M. H., Azouz, M. M., Abdelli, M. N., Boudabous, M., Feki, M., Fekih, M., Mahmoudi, M., Boudabbous, M., Figuigui, M., Medhioub, M., Safer, M., Azzouz, M., Abbes, M., El Abkari, M., Aqodad, N., Azib, N., Bellil, N., Benhoumane, N., Benzoubbeir, N., Elkhabiz, N., Hemdani, N., Lahmidani, N., Abdelli, N., Ben Chaabane, N., Tahri, N., Benhoummane, N., Ben Jaafar, N., Ben Mustapha, N., Maamouri, N., Hannachi, N., Ben Alaya, N., Bibani, N., Trad, N., Elleuch, N., Kharmach, O., Bahri, O., Bousnina, O., Gharbi, O., Benjira, R., Ennaifer, R., Dabbèche, R., Jouini, R., Zgolli, R., Baklouti, R., Bouali Mohamed, R., Marouani, R., Kallel, R., Berrag, S., El Yazal, S., Jiddi, S., Mechhour, S., Morabit, S., Oubaha, S., Sentissi, S., Bouaziz, S., Soua, S., Hachicha, S., Elaboudi, S., Ajmi, S., Mallat, S., Bouchoucha, S., Mrabti, S., Ben Slama, S., Hamdi, S., Laabidi, S., Ayadi, S., Hidri, S., Bizid, S., Ben Hamida, S., Zertiti, S., Ben Amor, S., Nsibi, S., Bellakhal, S., Bahja, S., Jomni, T., Hliwa, W., Rebai, W., Ben Mansour, W., Ben Othmen, W., Dhouib, W., Hammoumi, W., Zaatour, W., Bouhlel, W., Feki, W., Triki, W., Said, Y., Zaimi, Y., Gorgi, Y., Bouhnoun, Z., Samlani, Z., Hamidi, Z., Mnif, Z., and Ben Safta, Z.
34. Answering Queries in the Presence of XML Keys
- Author
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Essid, M., primary, Boucelma, O., additional, and Bressan, S., additional
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35. VirGIS: mediation for geographical information systems.
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Boucelma, O., Essid, M., Lacroix, Z., Vinel, J., Garinet, J.-Y., and Betari, A.
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- 2004
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36. Crystal Structural Characteristics and Electrical Properties of Novel Sol-Gel Synthesis of Ceramic Bi 0.75 Ba 0.25 (FeMn) 0.5 O 3 .
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Tayari F, Dhahri R, Elkenany EB, Teixeira SS, Graça MPF, Al-Syadi AM, Essid M, and Iben Nassar K
- Abstract
In this investigation, our primary objective is to explore the structural, morphological, and electrical characteristics of Bi
0.75 Ba0.25 (FeMn)0.5 O3 ceramic material synthesized by the sol-gel method. The prepared sample underwent synthesis through the conventional sol-gel technique. Examination through X-ray diffraction (XRD) unveiled a well-defined rhombohedral structure within the R3´C space group. Moreover, to evaluate the purity and nano-grain morphology, we utilized energy dispersive spectroscopy (EDX) and scanning electron microscopy (SEM). Electrical assessments were carried out over a frequency span of 100 Hz to 1 MHz and temperatures ranging from 200 to 340 K. Employing the correlated barrier hopping (CBH) model, we analyzed the AC conductivity of our specimen. The activation energy, determined from both DC conductivity and impedance spectra, demonstrated close correspondence, suggesting that both conductivity and r laxation processes are influenced by similar factors. Notably, the dielectric properties hold significant importance, potentially rendering our sample suitable for electronic applications. Furthermore, we calculated thermodynamic parameters, such as enthalpy (ΔH), entropy change (ΔS), and free energy of activation (ΔF), offering deeper insights into the material's behavior and conductivity mechanisms.- Published
- 2024
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37. Tailoring of structural, morphological, electrical, and magnetic properties of LaMn 1- x Fe x O 3 ceramics.
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Thakur P, Nassar KI, Kumar D, Kumar P, Sharma P, Tirth V, Alosaimy AS, Algahtani A, Essid M, and Lal M
- Abstract
This study undertakes a comparative analysis of the structural, morphological, electrical, and magnetic characteristics of Fe-doped LaMnO
3 ceramics. The solid-state reaction method was used to prepare Fe-doped LaMnO3 at different concentrations (0.00 ≤ x ≤ 1.00) and has been characterized using X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FE-SEM), energy-dispersive spectroscopy (EDS), and vibrating sample magnetometry (VSM). The structural transformation from rhombohedral to orthorhombic with Fe-doping is demonstrated by Rietveld's refined XRD patterns. The positive slope in Williamsons-Hall's (W-H) plots confirms the presence of tensile strain with increasing average crystallite size. Quasi-spherical morphology of all the compositions with similar uniformity was confirmed by FESEM images. The chemical distribution of all the elements has been identified by EDS mapping images. Normal dielectric dispersion behaviour of all the samples with NTCR response is confirmed by dielectric and impedance analysis respectively. Increasing lattice volume with Fe-concentration results is increasing Ea . The presence of antiferromagnetic ordering, in addition to weak ferromagnetic ordering, is indicated by the unsaturated magnetization even up to a high external field. The decrease in MS and increase in HC values due to Fe-doping reflect the influence of particle size on various magnetic parameters., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)- Published
- 2024
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38. RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.
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Maroofian R, Sarraf P, O'Brien TJ, Kamel M, Cakar A, Elkhateeb N, Lau T, Patil SJ, Record CJ, Horga A, Essid M, Selim L, Benrhouma H, Ben Younes T, Zifarelli G, Pagnamenta AT, Bauer P, Khundadze M, Mirecki A, Kamel SM, Elmonem MA, Ghayoor Karimiani E, Jamshidi Y, Offiah AC, Rossor AM, Youssef-Turki IB, Hübner CA, Munot P, Reilly MM, Brown AEX, Nagy S, and Houlden H
- Subjects
- Humans, Male, Female, Child, Adult, Adolescent, Young Adult, Middle Aged, Animals, Lower Extremity physiopathology, Caenorhabditis elegans, Muscle Spasticity genetics, Muscle Spasticity physiopathology, Spastic Paraplegia, Hereditary genetics, Spastic Paraplegia, Hereditary physiopathology, Mutation, Pedigree
- Abstract
Heterozygous RTN2 variants have been previously identified in a limited cohort of families affected by autosomal dominant spastic paraplegia (SPG12-OMIM:604805) with a variable age of onset. Nevertheless, the definitive validity of SPG12 remains to be confidently confirmed due to the scarcity of supporting evidence. In this study, we identified and validated seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven consanguineous families with distal hereditary motor neuropathy (dHMN) using exome, genome and Sanger sequencing coupled with deep-phenotyping. All affected individuals (seven males and seven females, aged 9-50 years) exhibited weakness in the distal upper and lower limbs, lower limb spasticity and hyperreflexia, with onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography. Despite a slowly progressive disease course, all patients remained ambulatory over a mean disease duration of 19.71 ± 13.70 years. Characterization of Caenorhabditis elegans RTN2 homologous loss-of-function variants demonstrated morphological and behavioural differences compared with the parental strain. Treatment of the mutant with an endoplasmic/sarcoplasmic reticulum Ca2+ reuptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences, suggesting a potential therapeutic benefit for RTN2-disorder. Despite RTN2 being an endoplasmic reticulum (ER)-resident membrane shaping protein, our analysis of patient fibroblast cells did not find significant alterations in ER structure or the response to ER stress. Our findings delineate a distinct form of autosomal recessive dHMN with pyramidal features associated with RTN2 deficiency. This phenotype shares similarities with SIGMAR1-related dHMN and Silver-like syndromes, providing valuable insights into the clinical spectrum and potential therapeutic strategies for RTN2-related dHMN., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain.)
- Published
- 2024
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39. Tuning the optoelectronic properties of selenophene-diketopyrrolopyrrole-based non-fullerene acceptor to obtain efficient organic solar cells through end-capped modification.
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Ijaz R, Waqas M, Mahal A, Essid M, Zghab I, Khera RA, Alotaibi HF, Al-Haideri M, Alshomrany AS, Zahid S, Alatawi NS, and Aloui Z
- Subjects
- Humans, Ketones, Electrons, Osteosclerosis, Pyrroles
- Abstract
With the goal of developing a high-performance organic solar cell, nine molecules of A
2 -D-A1 -D-A2 type are originated in the current investigation. The optoelectronic properties of all the proposed compounds are examined by employing the DFT approach and the B3LYP functional with a 6-31G (d, p) basis set. By substituting the terminal moieties of reference molecule with newly proposed acceptor groups, several optoelectronic and photovoltaic characteristics of OSCs have been studied, which are improved to a significant level when compared with reference molecule, i.e., absorption properties, excitation energy, exciton binding energy, band gap, oscillator strength, electrostatic potential, light-harvesting efficiency, transition density matrix, open-circuit voltage, fill factor, density of states and interaction coefficient. All the newly developed molecules (P1-P9) have improved λmax , small band gap, high oscillator strengths, and low excitation energies compared to the reference molecule. Among all the studied compounds, P9 possesses the least binding energy (0.24 eV), P8 has high interaction coefficient (0.70842), P3 has improved electron mobility due to the least electron reorganization energy (λe = 0.009182 eV), and P5 illustrates high light-harvesting efficiency (0.7180). P8 and P9 displayed better Voc results (1.32 eV and 1.33 eV, respectively) and FF (0.9049 and 0.9055, respectively). Likewise, the phenomenon of charge transfer in the PTB7-Th/P1 blend seems to be a marvelous attempt to introduce them in organic photovoltaics. Consequently, the outcomes of these parameters demonstrate that adding new acceptors to reference molecule is substantial for the breakthrough development of organic solar cells (OSCs)., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)- Published
- 2024
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40. Study of Electrical and Dielectric Behaviors of Copper-Doped Zinc Oxide Ceramic Prepared by Spark Plasma Sintering for Electronic Device Applications.
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Benamara M, Iben Nassar K, Rivero-Antúnez P, Essid M, Soreto Teixeira S, Zhao S, Serrà A, and Esquivias L
- Abstract
In this study, Cu-doped ZnO aerogel nanoparticles with a 4% copper concentration (Cu4ZO) were synthesized using a sol-gel method, followed by supercritical drying and heat treatment. The subsequent fabrication of Cu4ZO ceramics through Spark Plasma Sintering (SPS) was characterized by X-ray diffraction (XRD), field-emission gun scanning electron microscopy (FE-SEM) equipped with EDS, and impedance spectroscopy (IS) across a frequency range of 100 Hz to 1 MHz and temperatures from 270 K to 370 K. The SPS-Cu4ZO sample exhibited a hexagonal wurtzite structure with an average crystallite size of approximately 229 ± 10 nm, showcasing a compact structure with discernible pores. The EDS spectrum indicates the presence of the base elements zinc and oxygen with copper like the dopant element. Remarkably, the material displayed distinct electrical properties, featuring high activation energy values of about 0.269 ± 0.021 eV. Complex impedance spectroscopy revealed the impact of temperature on electrical relaxation phenomena, with the Nyquist plot indicating semicircular arc patterns associated with grain boundaries. As temperature increased, a noticeable reduction in the radius of these arcs occurred, coupled with a shift in their center points toward the axis center, suggesting a non-Debye-type relaxation mechanism. Dielectric analyses revealed a temperature-driven evolution of losses, emphasizing the material's conductivity impact. Non-Debye-type behavior, linked to ion diffusion, sheds light on charge storage dynamics. These insights advance potential applications in electronic devices and energy storage.
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- 2024
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41. A DFT study for improving the photovoltaic performance of organic solar cells by designing symmetric non-fullerene acceptors by quantum chemical modification on pre-existed LC81 molecule.
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Zahoor A, Sadiq S, Khera RA, Essid M, Aloui Z, Alatawi NS, Ibrahim MAA, Hasanin THA, and Waqas M
- Subjects
- Humans, Chlorhexidine, Osteosclerosis
- Abstract
Minimizing the energy loss and improving the open circuit voltage of organic solar cells is still a primary concern for scientists working in this field. With the aim to enhance the photovoltaic performance of organic solar cells by minimizing energy loss and improving open circuit voltage, seven new acceptor molecules (LC1-LC7) are presented in this work. These molecules are designed by modifying the terminal acceptors of pre-existed "LC81" molecule based on an indacinodithiophene (IDT) fused core. The end-group modification approach is very fruitful in ameliorating the efficacy and optoelectric behavior of OSCs. The newly developed molecules presented remarkable improvements in performance-related parameters and optoelectronic properties. Among all designed molecules, LC7 exhibited the highest absorption maxima (λ
max = 869 nm) with the lowest band-gap (1.79 eV), lowest excitation energy (Ex = 1.42 eV), lowest binding energy, and highest excited state lifetime (0.41 ns). The newly designed molecules LC2, LC3, and LC4 exhibited remarkably improved Voc that was 1.84 eV, 1.82 eV, and 1.79 eV accordingly, compared to the LC81 molecule with Voc of 1.74 eV LC2 molecule showed significant improvement in fill factor compared to the previously presented LC81 molecule. LC2, LC6, and LC7 showed a remarkable reduction in energy loss by showing Eloss values of 0.26 eV, 0.18 eV, and 0.25 eV than LC81 molecule (0.37 eV). These findings validate the supremacy of these developed molecules (especially LC2) as potential components of future OSCs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)- Published
- 2023
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42. Exploring the Electronic, Optical, and Charge Transfer Properties of A-D-A-Type IDTV-ThIC-Based Molecules To Enhance Photovoltaic Performance of Organic Solar Cells.
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Majeed M, Waqas M, Aloui Z, Essid M, Ibrahim MAA, Khera RA, Shaban M, and Ans M
- Abstract
Improving the charge mobility and optoelectronic properties of indacenodithiophene - based small molecule acceptors is a key challenge to improving overall efficiency. In this current research, seven newly designed molecules ( DT1-DT7 ) comprising the indacenodithiophene - based core are presented to tune energy levels, enhance charge mobility, and improve the photovoltaic performance of IDTV-ThIC molecules via density functional theory. All the molecules were designed by end-capped modification by substituting terminal acceptors of IDTV-ThIC with strong electron-withdrawing moieties. Among all the examined structures, DT1 has proved itself a superior molecule in multiple aspects, including higher λ
max in chloroform (787 nm) and gaseous phase (727 nm), narrow band gap (2.16 eV), higher electron affinity (3.31 eV), least excitation energy (1.57 eV), and improved charge mobility due to low reorganization energy and higher excited state lifetime (2.37 ns) when compared to the reference (IDTV-ThIC) and other molecules. DT5 also showed remarkable improvement in different parameters, such as the lowest exciton binding energy (0.41 eV), leading to easier charge moveability. The improved open-circuit voltage of DT4 and DT5 makes them proficient molecules exhibiting the charge transfer phenomenon. The enlightened outcomes of these molecules can pave a new route to develop efficient organic solar cell devices using these molecules, especially DT1 , DT4 , and DT5 ., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)- Published
- 2023
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43. High-Efficiency and Low-Energy-Loss Organic Solar Cells Enabled by Tuning the End Group Modification of the Terthiophene-Based Acceptor Molecules to Enhance Photovoltaic Properties.
- Author
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Rehman FU, Hameed S, Khera RA, Shaban M, Essid M, Aloui Z, Al-Saeedi SI, Ibrahim MAA, and Waqas M
- Abstract
In the current study, six nonfullerene small acceptor molecules were designed by end-group modification of terminal acceptors. Density functional theory calculations of all designed molecules were performed, and optoelectronic properties were computed by employing different functionals. Every constructed molecule has a significant bathochromic shift in the maximum absorption value (λ
max ) except AM6 . AM1 - AM4 molecules represented a narrow band gap ( Eg ) and low excitation energy values. The AM1 - AM4 and AM6 molecules have higher electron mobility. Comparing AM2 to the reference molecule reveals that AM2 has higher hole mobilities. Compared to the reference molecule, all compounds have excellent light harvesting efficiency values compared to AM1 and AM2 . The natural transition orbital investigation showed that AM5 and AM6 had significant electronic transitions. The open-circuit voltage ( Voc ) values of the computed molecules were calculated by combining the designed acceptor molecules with PTB7-Th. In light of the findings, it is concluded that the designed molecules can be further developed for organic solar cells (OSCs) with superior photovoltaic abilities., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)- Published
- 2023
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44. Enhanced detection of low concentration volatile organic compounds using advanced doped zinc oxide sensors.
- Author
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Benamara M, Ly A, Soltani S, Essid M, Dahman H, Dhahri R, El Mir L, Debliquy M, and Lahem D
- Abstract
Pure zinc oxide nanoparticles, as well as those doped with 3% calcium, aluminum, and gallium, were synthesized using a sol-gel method and then deposited onto an alumina substrate for sensing tests. The resulting nanoparticles were characterized using a variety of techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM) equipped with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), UV-VIS-NIR absorption spectroscopy, and photoluminescence (PL) measurements, to examine their structural, morphological, and optical properties. The prepared nanoparticles were found to have the hexagonal wurtzite structure of ZnO with a P 63 mC space group. The UV-Vis-IR spectra showed that the samples are highly absorbent in the UV range, while the PL spectra confirmed the presence of many defects in the ZnO structure, such as oxygen vacancies and zinc interstitials. The doped samples exhibited more defects than the pure sample. SEM images of the deposited film surface showed agglomerates with a spherical shape and confirmed the nanometer scale size of our prepared samples, as corroborated by the TEM images. The EDX spectra indicated the high purity of the ZnO deposited films, with a high presence of Zn and O and the presence of the doped elements (Ca, Al, and Ga) in each doped sample. Sensing tests were performed on ZnO, Ca
3% -doped ZnO (C3ZO), Al3% -doped ZnO (A3ZO), and Ga3% -doped ZnO (G3ZO) sensors in the presence of volatile organic compounds (VOCs) gases such as ethanol, formaldehyde, methanol, and acetone at low concentrations. The sensors exhibited high responses to low ppm level concentrations of the VOCs gases. At a low operational temperature of 250 °C, the C3ZO sensor had the highest response to 5 ppm of ethanol, methanol, and formaldehyde gases compared to the pure and other doped sensors. Additionally, the A3ZO sensor exhibited the highest response to acetone gas. In conclusion, our findings suggest that the doping of zinc oxide can enhance the low concentration detection of VOCs gases, with the C3ZO and A3ZO sensors showing the highest response to specific gases., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)- Published
- 2023
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45. Synergistic modification of end groups in Quinoxaline fused core-based acceptor molecule to enhance its photovoltaic characteristics for superior organic solar cells.
- Author
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Sadiq S, Waqas M, Zahoor A, Mehmood RF, Essid M, Aloui Z, Khera RA, and Akram SJ
- Subjects
- Prospective Studies, Quinoxalines
- Abstract
The competence of organic solar cells (OSCs) could be enhanced by improving the light absorption capabilities as well as the open-circuit voltage (V
oc ) of utilized molecules. To upgrade overall functionality of OSCs, seven new molecules were designed in this work using an end-cap alteration technique on Quinoxaline fused core-based non-fullerene acceptor (Qx-2) molecule. This technique is known to be quite advantageous in terms of improvement of the effectiveness and optoelectrical behavior of various OSCs. Critical parameters like the absorption maximum, frontier molecular orbitals, excitation energy, exciton binding energy, Voc , and fill factor of molecules were considered for the molecules thus designed. All newly designed molecules showed outstanding improvement in optoelectronic as well as performance-related properties. Out of all scrutinized molecules, Q1 exhibited highest wavelength of absorption peak (λmax = 779 nm) with the reduced band gap (1.90 eV), least excitation energy (Ex = 1.59 eV), along with the highest dipole moment (17.982950 D). Additionally, the newly designed compounds Q4, Q5, and Q6 exhibited significantly improved Voc s that were 1.55, 1.47, and 1.50 eV accordingly, as compared to the 1.37 eV of Qx-2 molecule. These molecules also showed remarkable improvement in fill factor attributed to direct correspondence of Voc with it. Inclusively, these results support the superiority of these newly developed molecules as prospective constituents of upgraded OSCs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)- Published
- 2023
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46. Magnetocaloric effect and critical behavior of the La 0.75 Ca 0.1 Na 0.15 MnO 3 compound.
- Author
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Bouzidi S, Hsini M, Soltani S, Essid M, Albedah MA, Belmabrouk H, and Dhahri J
- Abstract
In this paper, we have studied the critical behavior and the magnetocaloric effect (MCE) simulation for the La
0.75 Ca0.1 Na0.15 MnO3 (LCNMO) compound at the second order ferromagnetic-paramagnetic phase transition. The optimized critical exponents, based on the Kouvel-Fisher method, were found to be: β = 0.48 and γ = 1. These obtained values supposed that the Mean Field Model (MFM) is the proper model to analyze adequately the MCE in the LCNMO sample. The isothermal magnetization M ( H , T ) and the magnetic entropy change -Δ SM ( H , T ) curves were successfully simulated using three models, namely the Arrott-Noakes equation (ANE) of state, Landau theory, and MFM. The framework of the MFM allows us to estimate magnetic entropy variation in a wide temperature range within the thermodynamics of the model and without using the usual numerical integration of Maxwell relation., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)- Published
- 2023
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47. Theoretical framework for achieving high V oc in non-fused non-fullerene terthiophene-based end-capped modified derivatives for potential applications in organic photovoltaics.
- Author
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Waqas M, Hadia NMA, Shawky AM, Mahmood RF, Essid M, Aloui Z, Alatawi NS, Iqbal J, and Khera RA
- Abstract
Non-fused ring-based OSCs are an excellent choice, which is attributed to their low cost and flexibility in applications. However, developing efficient and stable non-fused ring-based OSCs is still a big challenge. In this work, with the intent to increase V
oc for enhanced performance, seven new molecules derived from a pre-existing A-D-A type A3T-5 molecule are proposed. Different important optical, electronic and efficiency-related attributes of molecules are studied using the DFT approach. It is discovered that newly devised molecules possess the optimum features required to construct proficient OSCs. They possess a small band gap ranging from 2.22-2.29 eV and planar geometries. Six of seven newly proposed molecules have less excitation energy, a higher absorption coefficient and higher dipole moment than A3T-5 in both gaseous and solvent phases. The A3T-7 molecule exhibited the maximum improvement in optoelectronic properties showing the highest λmax at 697 nm and the lowest Ex of 1.77 eV. The proposed molecules have lower ionization potential values, reorganization energies of electrons and interaction coefficients than the A3T-5 molecule. The Voc of six newly developed molecules is higher ( Voc ranging from 1.46-1.72 eV) than that of A3T-5 ( Voc = 1.55 eV). Similarly, almost all the proposed molecules except W6 exhibited improvement in fill factor compared to the A3T-5 reference. This remarkable improvement in efficiency-associated parameters ( Voc and FF) proves that these molecules can be successfully used as an advanced version of terthiophene-based OSCs in the future., Competing Interests: The Authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)- Published
- 2023
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48. Quantum modeling of dimethoxyl-indaceno dithiophene based acceptors for the development of semiconducting acceptors with outstanding photovoltaic potential.
- Author
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Rashid EU, Hadia NMA, Shawky AM, Ijaz N, Essid M, Iqbal J, Alatawi NS, Ans M, and Khera RA
- Abstract
In the current DFT study, seven dimethoxyl-indaceno dithiophene based semiconducting acceptor molecules (ID1-ID7) are designed computationally by modifying the parent molecule (IDR). Here, based on a DFT exploration at a carefully selected level of theory, we have compiled a list of the optoelectronic properties of ID1-ID7 and IDR. In light of these results, all newly designed molecules, except ID5 have shown a bathochromic shift in their highest absorbance ( λ
max ). ID1-ID4, ID6 and ID7 molecules have smaller band gap ( Egap ) and excitation energy ( Ex ). IP of ID5 is the smallest and EA of ID1 is the largest among all others. Compared to the parent molecule, ID1-ID3 have increased electron mobility, with ID1 being the most improved in hole mobility. ID4 had the best light harvesting efficiency in this investigation, due to its strongest oscillator. The acceptor molecules' open-circuit voltages ( VOC ) were computed after being linked to the PTB7-Th donor molecule. Fill factor (FF) and normalized VOC of ID1-ID7 were calculated and compared to the parent molecule. Based on the outcomes of this study, the modified acceptors may be further scrutinised for empirical usage in the production of organic solar cells with enhanced photovoltaic capabilities., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)- Published
- 2023
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49. Is YouTube™ a reliable source for patient information about Holmium Laser Enucleation of Prostate?
- Author
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Mokadem S, Fortier A, Gharbi M, Essid MA, Aublé A, Defortescu G, Pfister C, Sibert L, and Cornu JN
- Subjects
- Humans, Male, Prostate, Video Recording, Laser Therapy, Lasers, Solid-State therapeutic use, Prostatic Hyperplasia surgery, Social Media
- Abstract
Objectives: Prior to benign prostate surgery, the patient's informed consent is mandatory. Among the multiple source of information for patients, social networks are very popular, but the quality of information delivered is unknown. The aim of this study was to evaluate the quality of the information freely available for patients on YouTube™ regarding HoLEP., Materials and Methods: The term "HOLEP" was searched on YouTube™ on December 24, 2020. Videos that were not in English, French or Arabic, specifically destined to the medical community, with no written or oral comment, patient testimonials, pure surgical technique or had content unrelated to HoLEP were excluded from the study. The patient information sheet by the French Urology Association (AFU) was used to create a list of 31 items classified into 4 categories as follows: anatomy and pathophysiology (6 items), technique and perioperative preparation (10 items), usual outcomes (10 items) and complications (5 items). For each item on the predefined list, correct, missing and incorrect information were rated respectively 1, 0 and -1., Results: Thirty-five videos met the inclusion criteria. Their average length was 6'06"±7'03" [00'20"; 31'30"], with an average number of views of 5279±17,821 [8; 87,354]. The information provided on the videos was written and oral, oral-only and written-only in 51%, 34% and 14% of cases, respectively. 23% of the videos showed surgery sequences, 40% animations and 62% a doctor speaking. Only one video had a quality score greater than 80% and 7 videos got a score below 20%., Conclusion: The information about HoLEP on YouTube™ seemed not of sufficiently high quality to allow patients to make informed decisions, and was occasionally misleading. Surgeons still have the duty to give the best quality information, and may point patients towards adequate sources of information, especially those delivered by national and international professional societies., (Copyright © 2022 Elsevier Masson SAS. All rights reserved.)
- Published
- 2022
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50. 46th Medical Maghrebian Congress. November 9-10, 2018. Tunis.
- Author
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Alami Aroussi A, Fouad A, Omrane A, Razzak A, Aissa A, Akkad A, Amraoui A, Aouam A, Arfaoui A, Belkouchi A, Ben Chaaben A, Ben Cheikh A, Ben Khélifa A, Ben Mabrouk A, Benhima A, Bezza A, Bezzine A, Bourrahouat A, Chaieb A, Chakib A, Chetoui A, Daoudi A, Ech-Chenbouli A, Gaaliche A, Hassani A, Kassimi A, Khachane A, Labidi A, Lalaoui A, Masrar A, McHachi A, Nakhli A, Ouakaa A, Siati A, Toumi A, Zaouali A, Condé AY, Haggui A, Belaguid A, El Hangouche AJ, Gharbi A, Mahfoudh A, Bouzouita A, Aissaoui A, Ben Hamouda A, Hedhli A, Ammous A, Bahlous A, Ben Halima A, Belhadj A, Bezzine A, Blel A, Brahem A, Banasr A, Meherzi A, Saadi A, Sellami A, Turki A, Ben Miled A, Ben Slama A, Daib A, Zommiti A, Chadly A, Jmaa A, Mtiraoui A, Ksentini A, Methnani A, Zehani A, Kessantini A, Farah A, Mankai A, Mellouli A, Zaouali A, Touil A, Hssine A, Ben Safta A, Derouiche A, Jmal A, Ferjani A, Djobbi A, Dridi A, Aridhi A, Bahdoudi A, Ben Amara A, Benzarti A, Ben Slama AY, Oueslati A, Soltani A, Chadli A, Aloui A, Belghuith Sriha A, Bouden A, Laabidi A, Mensi A, Ouakaa A, Sabbek A, Zribi A, Green A, Ben Nasr A, Azaiez A, Yeades A, Belhaj A, Mediouni A, Sammoud A, Slim A, Amine B, Chelly B, Jatik B, Lmimouni B, Daouahi B, Ben Khelifa B, Louzir B, Dorra A, Dhahri B, Ben Nasrallah C, Chefchaouni C, Konzi C, Loussaief C, Makni C, Dziri C, Bouguerra C, Kays C, Zedini C, Dhouha C, Mohamed C, Aichaouia C, Dhieb C, Fofana D, Gargouri D, Chebil D, Issaoui D, Gouiaa D, Brahim D, Essid D, Jarraya D, Trad D, Ben Hmida E, Sboui E, Ben Brahim E, Baati E, Talbi E, Chaari E, Hammami E, Ghazouani E, Ayari F, Ben Hariz F, Bennaoui F, Chebbi F, Chigr F, Guemira F, Harrar F, Benmoula FZ, Ouali FZ, Maoulainine FMR, Bouden F, Fdhila F, Améziani F, Bouhaouala F, Charfi F, Chermiti Ben Abdallah F, Hammemi F, Jarraya F, Khanchel F, Ourda F, Sellami F, Trabelsi F, Yangui F, Fekih Romdhane F, Mellouli F, Nacef Jomli F, Mghaieth F, Draiss G, Elamine G, Kablouti G, Touzani G, Manzeki GB, Garali G, Drissi G, Besbes G, Abaza H, Azzouz H, Said Latiri H, Rejeb H, Ben Ammar H, Ben Brahim H, Ben Jeddi H, Ben Mahjouba H, Besbes H, Dabbebi H, Douik H, El Haoury H, Elannaz H, Elloumi H, Hachim H, Iraqi H, Kalboussi H, Khadhraoui H, Khouni H, Mamad H, Metjaouel H, Naoui H, Zargouni H, Elmalki HO, Feki H, Haouala H, Jaafoura H, Drissa H, Mizouni H, Kamoun H, Ouerda H, Zaibi H, Chiha H, Kamoun H, Saibi H, Skhiri H, Boussaffa H, Majed H, Blibech H, Daami H, Harzallah H, Rkain H, Ben Massoud H, Jaziri H, Ben Said H, Ayed H, Harrabi H, Chaabouni H, Ladida Debbache H, Harbi H, Yacoub H, Abroug H, Ghali H, Kchir H, Msaad H, Ghali H, Manai H, Riahi H, Bousselmi H, Limem H, Aouina H, Jerraya H, Ben Ayed H, Chahed H, Snéne H, Lahlou Amine I, Nouiser I, Ait Sab I, Chelly I, Elboukhani I, Ghanmi I, Kallala I, Kooli I, Bouasker I, Fetni I, Bachouch I, Bouguecha I, Chaabani I, Gazzeh I, Samaali I, Youssef I, Zemni I, Bachouche I, Youssef I, Bouannene I, Kasraoui I, Laouini I, Mahjoubi I, Maoudoud I, Riahi I, Selmi I, Tka I, Hadj Khalifa I, Mejri I, Béjia I, Bellagha J, Boubaker J, Daghfous J, Dammak J, Hleli J, Ben Amar J, Jedidi J, Marrakchi J, Kaoutar K, Arjouni K, Ben Helel K, Benouhoud K, Rjeb K, Imene K, Samoud K, El Jeri K, Abid K, Chaker K, Abid K, Bouzghaîa K, Kamoun K, Zitouna K, Oughlani K, Lassoued K, Letaif K, Hakim K, Cherif Alami L, Benhmidoune L, Boumhil L, Bouzgarrou L, Dhidah L, Ifrine L, Kallel L, Merzougui L, Errguig L, Mouelhi L, Sahli L, Maoua M, Rejeb M, Ben Rejeb M, Bouchrik M, Bouhoula M, Bourrous M, Bouskraoui M, El Belhadji M, El Belhadji M, Essakhi M, Essid M, Gharbaoui M, Haboub M, Iken M, Krifa M, Lagrine M, Leboyer M, Najimi M, Rahoui M, Sabbah M, Sbihi M, Zouine M, Chefchaouni MC, Gharbi MH, El Fakiri MM, Tagajdid MR, Shimi M, Touaibia M, Jguirim M, Barsaoui M, Belghith M, Ben Jmaa M, Koubaa M, Tbini M, Boughdir M, Ben Salah M, Ben Fraj M, Ben Halima M, Ben Khalifa M, Bousleh M, Limam M, Mabrouk M, Mallouli M, Rebeii M, Ayari M, Belhadj M, Ben Hmida M, Boughattas M, Drissa M, El Ghardallou M, Fejjeri M, Hamza M, Jaidane M, Jrad M, Kacem M, Mersni M, Mjid M, Sabbah M, Serghini M, Triki M, Ben Abbes M, Boussaid M, Gharbi M, Hafi M, Slama M, Trigui M, Taoueb M, Chakroun M, Ben Cheikh M, Chebbi M, Hadj Taieb M, Kacem M, Ben Khelil M, Hammami M, Khalfallah M, Ksiaa M, Mechri M, Mrad M, Sboui M, Bani M, Hajri M, Mellouli M, Allouche M, Mesrati MA, Mseddi MA, Amri M, Bejaoui M, Bellali M, Ben Amor M, Ben Dhieb M, Ben Moussa M, Chebil M, Cherif M, Fourati M, Kahloul M, Khaled M, Machghoul M, Mansour M, Abdesslem MM, Ben Chehida MA, Chaouch MA, Essid MA, Meddeb MA, Gharbi MC, Elleuch MH, Loueslati MH, Sboui MM, Mhiri MN, Kilani MO, Ben Slama MR, Charfi MR, Nakhli MS, Mourali MS, El Asli MS, Lamouchi MT, Cherti M, Khadhraoui M, Bibi M, Hamdoun M, Kassis M, Touzi M, Ben Khaled M, Fekih M, Khemiri M, Ouederni M, Hchicha M, Kassis M, Ben Attia M, Yahyaoui M, Ben Azaiez M, Bousnina M, Ben Jemaa M, Ben Yahia M, Daghfous M, Haj Slimen M, Assidi M, Belhadj N, Ben Mustapha N, El Idrissislitine N, Hikki N, Kchir N, Mars N, Meddeb N, Ouni N, Rada N, Rezg N, Trabelsi N, Bouafia N, Haloui N, Benfenatki N, Bergaoui N, Yomn N, Ben Mustapha N, Maamouri N, Mehiri N, Siala N, Beltaief N, Aridhi N, Sidaoui N, Walid N, Mechergui N, Mnif N, Ben Chekaya N, Bellil N, Dhouib N, Achour N, Kaabar N, Mrizak N, Mnif N, Chaouech N, Hasni N, Issaoui N, Ati N, Balloumi N, Haj Salem N, Ladhari N, Akif N, Liani N, Hajji N, Trad N, Elleuch N, Marzouki NEH, Larbi N, M'barek N, Rebai N, Bibani N, Ben Salah N, Belmaachi O, Elmaalel O, Jlassi O, Mihoub O, Ben Zaid O, Bouallègue O, Bousnina O, Bouyahia O, El Maalel O, Fendri O, Azzabi O, Borgi O, Ghdes O, Ben Rejeb O, Rachid R, Abi R, Bahiri R, Boulma R, Elkhayat R, Habbal R, Rachid R, Tamouza R, Jomli R, Ben Abdallah R, Smaoui R, Debbeche R, Fakhfakh R, El Kamel R, Gargouri R, Jouini R, Nouira R, Fessi R, Bannour R, Ben Rabeh R, Kacem R, Khmakhem R, Ben Younes R, Karray R, Cheikh R, Ben Malek R, Ben Slama R, Kouki R, Baati R, Bechraoui R, Fakhfakh R, Fradi R, Lahiani R, Ridha R, Zainine R, Kallel R, Rostom S, Ben Abdallah S, Ben Hammamia S, Benchérifa S, Benkirane S, Chatti S, El Guedri S, El Oussaoui S, Elkochri S, Elmoussaoui S, Enbili S, Gara S, Haouet S, Khammeri S, Khefecha S, Khtrouche S, Macheghoul S, Mallouli S, Rharrit S, Skouri S, Helali S, Boulehmi S, Abid S, Naouar S, Zelfani S, Ben Amar S, Ajmi S, Braiek S, Yahiaoui S, Ghezaiel S, Ben Toumia S, Thabeti S, Daboussi S, Ben Abderahman S, Rhaiem S, Ben Rhouma S, Rekaya S, Haddad S, Kammoun S, Merai S, Mhamdi S, Ben Ali R, Gaaloul S, Ouali S, Taleb S, Zrour S, Hamdi S, Zaghdoudi S, Ammari S, Ben Abderrahim S, Karaa S, Maazaoui S, Saidani S, Stambouli S, Mokadem S, Boudiche S, Zaghbib S, Ayedi S, Jardek S, Bouselmi S, Chtourou S, Manoubi S, Bahri S, Halioui S, Jrad S, Mazigh S, Ouerghi S, Toujani S, Fenniche S, Aboudrar S, Meriem Amari S, Karouia S, Bourgou S, Halayem S, Rammeh S, Yaïch S, Ben Nasrallah S, Chouchane S, Ftini S, Makni S, Manoubi S, Miri S, Saadi S, Manoubi SA, Khalfallah T, Mechergui T, Dakka T, Barhoumi T, M'rad TEB, Ajmi T, Dorra T, Ouali U, Hannachi W, Ferjaoui W, Aissi W, Dahmani W, Dhouib W, Koubaa W, Zhir W, Gheriani W, Arfa W, Dougaz W, Sahnoun W, Naija W, Sami Y, Bouteraa Y, Elhamdaoui Y, Hama Y, Ouahchi Y, Guebsi Y, Nouira Y, Daly Y, Mahjoubi Y, Mejdoub Y, Mosbahi Y, Said Y, Zaimi Y, Zgueb Y, Dridi Y, Mesbahi Y, Gharbi Y, Hellal Y, Hechmi Z, Zid Z, Elmouatassim Z, Ghorbel Z, Habbadi Z, Marrakchi Z, Hidouri Z, Abbes Z, Ouhachi Z, Khessairi Z, Khlayfia Z, Mahjoubi Z, and Moatemri Z
- Subjects
- Africa, Northern epidemiology, Anatomy education, Education, Medical history, Education, Medical methods, Education, Medical organization & administration, History, 21st Century, Humans, Internship and Residency standards, Internship and Residency trends, Job Satisfaction, Pathology, Clinical education, Tunisia epidemiology, Education, Medical trends, Medicine methods, Medicine organization & administration, Medicine trends
- Published
- 2019
Catalog
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