Search Results - "Sbaï, Mohamed Hédi"

Lack of association between FokI polymorphism in vitamin D receptor gene (VDR) & type 2 diabetes mellitus in the Tunisian population by Mahjoubi, Imen, Kallel, Amani, Sbaï, Mohamed, Ftouhi, Bochra, ben Halima, Meriam, Jemaa, Zeineb, Feki, Moncef, Slimane, Hedia, Jemaa, Riadh, Kaabachi, Naziha

“…Background & objectives: The impact of several environmental and genetic factors on diabetes is well documented. Though the association between the vitamin D…”
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Polymorphisms of the NOS3 gene and risk of myocardial infarction in the Tunisian population by Kallel, Amani, Sbaï, Mohamed Hédi, Sediri, Yousra, Abdessalem, Salem, Mourali, Mohamed Sami, Feki, Moncef, Mechmeche, Rachid, Jemaa, Riadh, Kaabachi, Naziha

“…•308 Patients with MI and 225 controls were included in the study.•Glu298Asp, −786T/C and 4a4b polymorphisms of the NOS3 gene were studied in Tunisians.•These…”
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The paraoxonase L55M and Q192R gene polymorphisms and myocardial infarction in a Tunisian population by Kallel, Amani, Sediri, Yousra, Sbaï, Mohamed Hédi, Mourali, Mohamed Sami, Feki, Moncef, Elasmi, Monia, Taieb, Samah Haj, Sanhaji, Haïfa, Souheil, Omar, Mechmeche, Rachid, Jemaa, Riadh, Kaabachi, Naziha

“…In the present study, we examined a possible association between the PON1 Q192R and L55M polymorphisms and myocardial infarction (MI) in a sample of the…”
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Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population by Kallel, Amani, Sbaï, Mohamed Hedi, Sédiri, Yousra, Feki, Moncef, Mourali, Mohamed Sami, Mechmeche, Rachid, Jemaa, Riadh, Kaabachi, Naziha

“…The prothrombin is the precursor of the serine protease thrombin, a key enzyme in homeostasis. Prothrombin G20210A polymorphism (rs1799963) was described as a…”
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0183: A common polymorphism in CD40 Kozak sequence (-1C/T) is associated with myocardial infraction in the Tunisian male population by Jemaa, Riadh, Kallel, Amani, Wafi, Safa Ben, Sbaï, Mohamed Hédi, Mechmeche, Rachid, Kaabachi, Naziha

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0185: Prevalence of conventional risk factors in 44154 Tunisians patients with coronary heart disease by Jemaa, Riadh, Kallel, Amani, Sbaï, Mohamed Hédi, Rabie, Razgallah, Kafsi, Mohamed Naceur, Zaouali, R.M, Mechmeche, Rachid, Haouala, Habib, Slimane, M.L, Belhani, A., Ben Khalfallah, A., Gamra, H., Maatouk, F., Ammar, H., Chaouech, A., Boughzala, E., Bouajina, A., Chehaibi, N.

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Association between paraoxonase-1 gene promoter -108C/T polymorphism and myocardial infarction in the Tunisian male population / Tunuslu erkek populasyonunda miyokard enfarktüs ile paraoksonaz -1 gen başlatıcı -108C/T polimorfizmi arasındaki ilişki by Sbai, Mohamed Hédi, Kallel, Amani, Sediri, Yousra, Lassoued, Mehdi, Feki, Moncef, Mourali, Mohamed Sami, Kaabachi, Naziha, Jemaa, Riadh

“…Objective: Human paraoxonase 1 (PON1) is an HDL-associated enzyme with anti-oxidant/anti-inflammatory properties that has been suggested to play an important…”
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0184: Genetic association between single nucleotide polymorphisms in the Paraoxonase 1 (PON1) gene and the risk of myocardial infarction in the Tunisian male population by Sbai, Mohamed Hedi, Kallel, Amani, Sediri, Yousra, Lassoued, Mehdi, Mechmeche, Rachid, Jemaa, Riadh, Kaabachi, Naziha

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0501: Association of Cys311Ser polymorphism of paraoxonase-2 gene with myocardial infarction in the Tunisian male population by Sbai, Mohamed Hedi, Kallel, Amani, Sediri, Yousra, Daoued, Rim, Feki, Moncef, Mourali, Mohamed Sami, Jemaa, Riadh, Kaabachi, Naziha

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