Search Results - "Belhedi, Nejla"

Factor VIII haplotypes frequencies in Tunisian hemophiliacs A by Elmahmoudi, Hejer, Belhedi, Nejla, Jlizi, Asma, Zahra, Kaouther, Meddeb, Balkis, Ben Ammar Elgaaied, Amel, Gouider, Emna

“…The development of inhibitors against factor 8 (F8) is the most serious complication of replacement therapy with F8 in children with severe hemophilia. It was…”
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The Glanzmann's Thrombasthenia in Tunisia: A Cohort Study by Elmahmoudi, Hejer, Achour, Meriem, Belhedi, Nejla, Ben Neji, Hend, Zahra, Kaouther, Meddeb, Balkis, Gouider, Emna

“…The Glanzmann's thrombasthenia (GT) is a rare autosomal-recessive bleeding disorder with uncommon neonatal revelation. It is due to abnormalities of…”
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Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency by Abdallah, Hejer Elmahmoudi, Gouider, Emna, Stambouli, Nejla, Amor, Mohamed Ben, Jlizi, Asma, Belhedi, Nejla, Sassi, Rim, Khodjetelkhil, Houssein, Meddeb, Balkis, Hafsia, Raouf, Hamza, Adel, Elgaaied, Amel Benammar

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A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family by Belhedi, Nejla, Bena, Frédérique, Mrabet, Amel, Guipponi, Michel, Souissi, Chiraz Bouchlaka, Mrabet, Hela Khiari, Elgaaied, Amel Benammar, Malafosse, Alain, Salzmann, Annick

“…Genetic epilepsy with febrile seizures plus (GEFS+) is a familial epilepsy syndrome with extremely variable expressivity. The aim of our study was to identify…”
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Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency by Abdallah, Hejer Elmahmoudi, Gouider, Emna, Stambouli, Nejla, Ben Amor, Mohamed, Jlizi, Asma, Belhedi, Nejla, Sassi, Rim, Khodjetelkhil, Houssein, Meddeb, Balkis, Hafsia, Raouf, Hamza, Adel, Elgaaied, Amel Benammar

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