Genetic diseases in the Tunisian population von Romdhane, Lilia, Abdelhak, Sonia

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Benzene Exposure Monitoring of Tunisian Workers von Chakroun, Radhouane, Kaabachi, Néziha, Hedhili, Abderrazek, Feki, Moncef, Nouaigui, Habib, Laiba, Mohamed Ben, Mebazaa, Abderraouf

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Benzene exposure monitoring of Tunisian workers von CHAKROUN, Radhouane, KAABACHI, Néziha, HEDHILI, Abderrazek, FEKI, Moncef, NOUAIGUI, Habib, MOHAMED BEN LAIBA, MEBAZAA, Abderraouf

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0139: Detection of myocardial fibrosis in patients with hypertrophic cardiomyopathy evaluated by biological markers von Zaroui, Amira, Asmi, Monia, Fourty, Nesrine, Said, Rym Ben, Benhalima, Manel, Mourali, Mohamed Sami, Kaabachi, Neziha, Mechmeche, Rachid

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Predictors for cardiovascular morbidity and overall mortality in Tunisian ESRD patients: A six year prospective study von Fellah, Hayet, Hammami, Mohamed Bassem, Feki, Moncef, Boubaker, Karima, Abdallah, Taieb Ben, Lacour, Bernard, Mebazaa, Abderraouf, Kaabachi, Neziha

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Hyperhomocysteinemia is associated with deep venous thrombosis of the lower extremities in Tunisian patients von Omar, Souheil, Ghorbel, Imed Ben, Feki, Habib, Souissi, Malek, Feki, Moncef, Houman, Habib, Kaabachi, Neziha

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073 Association of coronary atherosclerosis diffusion, Framimgham score (FRS) and the metabolic syndrome (MS) and its component: anangiography study von Elasmi, Monia, Zidi, Wiem, Zayani, Yosra, Zaroui, Amira, Mechmeche, Rachid, Mourali, Sami, Kaabachi, Neziha

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Pyroglutamic aciduria von Naija, Ouns, Kaabachi, Neziha, Lakhoua, Mohamed Rachid

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Is serum transthyretin a reliable marker of nutritional status in patients with end-stage renal disease? von Fellah, Hayet, Omar, Souheil, Feki, Moncef, Abderrahim, Ezzedine, Abdallah, Taieb Ben, Massy, Ziad A., Lacour, Bernard, Maiz, Hedi Ben, Kaabachi, Neziha, Mebazaa, Abderraouf

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Serum leptin concentration in Tunisian non obese children von Jmal, Aouatef, Bouyahya, Olfa, Ayadi, Imène, Occhi, Hanène, Feki, Moncef, Kaabachi, Neziha, Sammoud, Azza, Abdennebi, Monia, Boukthir, Samir

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Phenylketonuria: An Underlying Etiology of Autistic Syndrome. A Case Report von Miladi, Najoua, Larnaout, Abdelmajid, Kaabachi, Neziha, Helayem, Mohamed, Ben Hamida, Mongi

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Serum leptin concentration in Tunisian non overweight non obese children von Jmal, Aouatef, Bouyahya, Olfa, Ayadi, Imène, Occhi, Hanène, Feki, Moncef, Kaabachi, Neziha, Sammoud, Azza, Abdennebi, Monia, Boukthir, Samir

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Hyperhomocysteinaemia is associated with uveitis but not with deep venous thrombosis in Behçet's disease von Feki, Moncef, Houman, Habib, Ghannouchi, Mehdi, Smiti-Khanfir, Monia, Hamzaoui, Kamel, Matri, Leila El, Mebazaa, Abderraouf, Kaabachi, Neziha

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C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine levels in obese Tunisian children von Gara, Sonia, Ochi, Hanene, Chango, Abalo, Najjar, Latifa, Feki, Moncef, B'chir, Fattouma, Kaabachi, Neziha, Ben Becher, Saayda, Boukthir, Samir, Abdennebi, Monia

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Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation von Moumni, Imen, Zorai, Amine, Ben Daoued, Bechir, Mosbahi, Ikbel, Omar, Souheil, Kaabachi, Neziha, Dellagi, Koussay, Abbes, Salem

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029 Prognostic value of cortisol, insulin and thyroid hormones levels in ST elevation acute myocardial infarction von Mghaieth, Fathia, Trabelsi, Ramy, Ellouze, Yassine, Amira, Zaroui, Ayadi, Imen, Feki, Moncef, Mourali, Sami, Kaabachi, Neziha, Mechmèche, Rachid, Zouari, Béchir

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Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation von Moumni, Imen, Zorai, Amine, Daoued, Bechir Ben, Mosbahi, Ikbel, Omar, Souheil, Kaabachi, Neziha, Dellagi, Koussay, Abbes, Salem

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Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) 0-Thalassemia Mutation von Moumni, Imen, Zorai, Amine, Ben Daoued, Bechir, Mosbahi, Ikbel, Omar, Souheil, Kaabachi, Neziha, Dellagi, Koussay, Abbes, Salem

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Hb A 2 -Pasteur-Tunis [δ59(E3)Lys→Asn, AA G →AA C ]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β 0 -Thalassemia Mutation von Moumni, Imen, Zorai, Amine, Ben Daoued, Bechir, Mosbahi, Ikbel, Omar, Souheil, Kaabachi, Neziha, Dellagi, Koussay, Abbes, Salem

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Hyperhomocysteinemia and End-Stage Renal Disease: Determinants and Association with Cardiovascular Disease in Tunisian Patients von Fellah, Hayet, Feki, Moncef, Hsairi, Mohamed, Sanhaji, Haifa, Kaabachi, Neziha, Abdallah, Taieb Ben, Massy, Ziad A., Maiz, Hedi Ben, Lacour, Bernard, Mebazaa, Abderraouf

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