Levothyroxine liquid oral substitution as an alternative treatment for refractory hypothyroidism due to gastrointestinal malabsorption: A case report von Cherchir, Faten, Oueslati, Ibtissem, Mouelhi, Yasmine, Talbi, Emna, Feki, Moncef, Yazidi, Meriem, Chihaoui, Melika

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Spectrum of Organic Aciduria Diseases in Tunisia: A 35-year Retrospective Study von Jelassi, Awatef, Nasrallah, Fahmi, Talbi, Emna, Hammami, Mohamed Bassem, Ghodbane, Rihab, Sanhaji, Haifa, Feki, Moncef, Kaabachi, Naziha, Hadj-Taieb, Sameh

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Evaluation of anthropometric profile in obese children: risk factors & eating disorder von Ben Othman, rym, Talbi, emna, Mizouri, ramla, Ben Amor, nadia, Gamoudi, amel, Lahmer, ines, Berriche, olfa, Mahjoub, faten, Jamoussi, henda

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Polymorphisms in NQO1 and MPO genes and risk for bladder cancer in Tunisian population von Hemissi, Imen, Ayed, Haroun, Naimi, Zeineb, Meddeb, Khedija, Ayadi, Mouna, Zouari, Skander, Zaghbib, Selim, Talbi, Emna, Chebil, Mohamed, Ouerhani, Slah

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Association of selected adipokines with metabolic syndrome and cardio-metabolic risk factors in young males von Ouerghi, Nejmeddine, Ben Fradj, Mohamed Kacem, Talbi, Emna, Bezrati, Ikram, Feki, Moncef, Bouassida, Anissa

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Mortality in decompensated cirrhotic patients and relationship with procalcitonin value von Lahiani, Sirine, Bouzid, Kahena, Khedher, Sana, Maoui, Amira, Bartkiz, Ahlem, Talbi, Emna, Hammami, Sana, Salem, Mohamed, Abdelmoula, Jaouida

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Prevalence and risk factors of hypogonadism in men with chronic renal failure von Oueslati, Ibtissem, Ounissi, Mondher, Talbi, Emna, Azaiez, Seifeddine, Bacha, Mohamed Mongi, Ben Abdallah, Taieb

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Non-alcoholic fatty liver disease and cardiovascular risk in patients with type 2 diabetes mellitus von Sebai, Imen, Oueslati, Ibtissem, Talbi, Emna, El Feleh, Emna, Grira, Wafa, Yazidi, Meriem, Chaker, Fatma, Chihaoui, Melika

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Correlations between B type natriuretic peptide and blood pressure in patients with type 2 diabetes mellitus von Sebai, Imen, Oueslati, Ibtissem, Khessairi, Nadia, Talbi, Emna, Yazidi, Meriem, Grira, Wafa, Chaker, Fatma, Chihaoui, Melika

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Predictive factors of macroangiopathy in type 2 diabetic patients von Sebai, Imen, Oueslati, Ibtissem, Khessairi, Nadia, Yazidi, Meriem, Talbi, Emna, Chaker, Fatma, Chihaoui, Melika

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Prevalence of vitamin D deficiency in mothers and their newborns in a Tunisian population von Ayadi, Imene D, Nouaili, Emira B.H, Talbi, Emna, Ghdemssi, Aicha, Rached, Chiraz, Bahlous, Afef, Gammoudi, Amel, Hamouda, Sonia Ben, Bouguerra, Badreddine, Bouzid, Kehna, Abdelmoula, Jouda, Marrakchi, Zahra

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MP108PRIMARY HYPEROXALIURIA: TUNISIAN NEPHROLOGY DEPARTMENT EXPERIENCE von Meriam, Hajji, Hayet, Kaaroud, Amel, Harzallah, Taieb, Ben Abdallah, Haroun, Ayed, Amine, Derouich, Riadh, Ben Slama, Med Cherif, Chebil, Emna, Talbi, Hanene, Baccouch, Jaouida, Abdelmoula, Saoussen, Mdimeg, Asma, Omezzine, Fethi, Ben Hamida

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Purple urine bag syndrome, a disturbing urine discoloration von Karray, Omar, Batti, Rym, Talbi, Emna, Ayed, Haroun, Chakroun, Marouene, Ouarda, Mouna Ayadi, Bouzouita, Abderrazek, Cherif, Mohamed, Ben Slama, Mohamed Riadh, Amel, Mezlini, Abdelmoula, Jouida, Derouiche, Amine, Chebil, Mohamed

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Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene von Abbes, Salem, Ghanem, Abderraouf, Chaouachi, Dorra, Kalai, Miniar, Ben Chaabene, Arij, Moumni, Imen, Talbi, Emna, Chaouch, Leila, Mallouli, Fethi

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Nephrolithiasis in living kidney donor: experience of nephrologists von Kaaroud, Hayet, Harzallah, Amel, Najjar, Mariem, Chtioui, Nour Houda, Cherif, Mohamed, Ayed, Haroun, Kerkeni, W, Bouzouita, A, Chebil, M, Talbi, Emna, Baccouch, Hanene, Benzarti, Amal, Abdelmoula, Jaouida, Benhamida, Fethi, Ben Abdallah, Taieb

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Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene von Chaouch, Leila, Talbi, Emna, Moumni, Imen, Ben Chaabene, Arij, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Ghanem, Abderraouf, Abbes, Salem

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Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene von Chaouch, Leila, Talbi, Emna, Moumni, Imen, Ben Chaabene, Arij, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Ghanem, Abderraouf, Abbes, Salem

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46th Medical Maghrebian Congress. November 9-10, 2018. Tunis von 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, Abdeddayem, Belaguid, Abdelaziz, El Hangouche, Abdelkader Jalil, Gharbi, Abdelkarim, Mahfoudh, Abdelmajid, Bouzouita, Abderrazek, Aissaoui, Abir, Ben Hamouda, Abir, Hedhli, Abir, Ammous, Adel, Bahlous, Afef, Ben Halima, Afef, Belhadj, Ahlem, Bezzine, Ahlem, Blel, Ahlem, Brahem, Ahlem, Banasr, Ahmed, Meherzi, Ahmed, Saadi, Ahmed, Sellami, Ahmed, Turki, Ahmed, Ben Miled, Aicha, Ben Slama, Aida, Daib, Aida, Zommiti, Alaa, Chadly, Ali, Jmaa, Ali, Mtiraoui, Ali, Ksentini, Alia, Methnani, Alia, Zehani, Alya, Kessantini, Amal, Farah, Amani, Mankai, Amani, Mellouli, Amani, Zaouali, Amani, Touil, Amany, Hssine, Ameni, Ben Safta, Amine, Derouiche, Amine, Jmal, Amine, Ferjani, Amir, Djobbi, Amira, Dridi, Amira, Aridhi, Amna, Bahdoudi, Anis, Ben Amara, Anis, Benzarti, Anis, Ben Slama, Anouar Youssef, Oueslati, Anouer, Soltani, Aouatef, Chadli, Aschraf, Aloui, Asma, Belghuith Sriha, Asma, Bouden, Asma, Laabidi, Asma, Mensi, Asma, Ouakaa, Asma, Sabbek, Asma, Zribi, Asma, Green, Assia, Ben Nasr, Atef, Azaiez, Aymen

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Levothyroxine liquid oral substitution as an alternative treatment for refractory hypothyroidism due to gastrointestinal malabsorption: A case report von Cherchir, Faten, Oueslati, Ibtissem, Mouelhi, Yasmine, Talbi, Emna, Feki, Moncef, Yazidi, Meriem, Chihaoui, Melika

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Purple urine bag syndrome, a disturbing urine discoloration von Karray, Omar, Batti, Rym, Talbi, Emna, Ayed, Haroun, Chakroun, Marouene, Ouarda, Mouna Ayadi, Bouzouita, Abderrazek, Cherif, Mohamed, Ben Slama, Mohamed Riadh, Amel, Mezlini, Abdelmoula, Jouida, Derouiche, Amine, Chebil, Mohamed

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