Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Mongi Hamdi"'
3
Groundwater quality delineation based on AHP method and GIS: a case study in Regueb basin, Central-Tunisia
Autor: rim missaoui, Kaouther NCIBI, bilel Abdelkarim, Abedlhakim Bouagila, Abedjabbar Choura, Mongi HAMDI, Younes HAMED
The Regueb basin constitutes an important agricultural area in Sidi Bouzid region (central Tunisia). Water scarcity and quality degradation propose an adequate management strategy. This strategy influenced by several parameters. In this context, the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::68e4d78974668abe44a6fdfd5f858f75
https://doi.org/10.21203/rs.3.rs-1602041/v1
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4
Application of the analytic hierarchy process to weight the criteria used to determine the Water Quality Index of groundwater in the northeastern basin of the Sidi Bouzid region, Central Tunisia
Autor: Kaouther Ncibi, Rihab Hadji, Mongi Hamdi, Naziha Mokadem, Malika Abbes, Faten Khelifi, Karim Zighmi, Younes Hamed
The Sidi Bouzid and El Hjal Wadi basins together comprise one of the most important agricultural regions in Central Tunisia. Exploitation of the groundwater in this region is increasing exponentially. In this work, hydrochemical characteristics and t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b5c452972e523d260a1c777ddb6d52
https://hdl.handle.net/10394/34672
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6
A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome
Autor: Souheil Omar, Ali Belhani, Mongi Hamdi, Judith C. Fleming, Charles I. Berul, Ellis J. Neufeld, Mara P. Steinkamp, Raouf Hafsia, Elena Tartaglini, Sarrah Baltagi-Ben Jilani, Sami Gritli, Souha Guannouni
Publikováno v: British Journal of Haematology. 113:508-513
Thiamine-responsive megaloblastic anaemia (TRMA) syndrome with diabetes and deafness was found in two patients from a Tunisian kindred. The proband was homozygous for a novel mutation, 287delG, in the high-affinity thiamine transporter gene, SLC19A2.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c4e8afa814e6c20beb265a6d5e5bbedc
https://doi.org/10.1046/j.1365-2141.2001.02774.x
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Plný text Recenzováno Digitální knihovna AV ČR
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