Search Results - "Hajer, Foddha"

The association between Dental Fluorosis and COL1A2 gene polymorphism among a Tunisian Population by Kallala, Rim, Slimani, Afef, Gassara, Yosra, Garrach, Behaeddin, Chouchen, Sawssen, Foddha, Hajer, Rouis, Asma, Kenani, Aberraouf

“…Dental fluorosis (DF) is a prevalent developmental defect of tooth enamel caused by exposure to excessive fluoride, with the severity dependent on various…”
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Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype? by Touhami, Rahma, Foddha, Hajer, Alix, Eudeline, Jalloul, Afef, Mougou-Zerelli, Soumaya, Saad, Ali, Sanlaville, Damien, Haj Khelil, Amel

“…Psychomotor delay, epilepsy and dysmorphic features are clinical signs which are described in multiple syndromes due to chromosomal imbalances or mutations…”
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Involvement of CXCL10 rs4256246, CXCR4 rs2228014, CCR2 rs1799864 and CXCL16 rs2277680 in the Predisposition to Schizophrenia by Saoud, Hana, Foddha, Hajer, Aflouk, Youssef, Jrad, Besma Bel Hadj

“…Chemokine ligands and their receptors have acquired less attention than pro- and anti-inflammatory cytokines in schizophrenia (SCZ). Thus, we aimed to examine…”
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Genetic polymorphisms in VEGFA and VEGFR2 genes associated with coronary heart disease susceptibility and severity by Hajer, Foddha, Hana, Saoud, Saoussen, Chouchene, Abdelhak, Foddha, Nadia, Bouzidi, Ameni, Dhiflaoui, Habib, Gamra, Hassen, Ben abdennebi, Amel, Haj Khelil

“…Background ​Vascular endothelial growth factor A ( VEGFA ) is well acknowledged as a powerful angiogenesis-promoting agent mainly through its receptor VEGFR2 …”
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Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction by Foddha, Hajer, Bouzidi, Nadia, Foddha, Abdelhak, Chouchene, Saoussen, Touhami, Rahma, Leban, Nadia, Maatoug, Mohamed Faouzi, Gamra, Habib, Ferchichi, Salima, Chibani, Jemni Ben, Khelil, Amel Haj

“…Coronary artery disease (CAD) and its ultimate consequence - myocardial infarction (MI) - are major causes of sudden cardiac death (SCD). Previous studies have…”
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Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype? by Touhami, Rahma, Foddha, Hajer, Alix, Eudeline, Jalloul, Afef, Mougou-Zerelli, Soumaya, Saad, Ali, Sanlaville, Damien, Haj Khelil, Amel

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