Search Results - "ELborgi, Wejden"

Coexistence of JAK2V617F and CALR mutation in Tunisian cohort with Philadelphia-negative chronic myeloproliferative neoplasms by Elmahmoudi, Hejer, Chourouk, Jbali, Wejden, Elborgi, Ons, Ghali, Kouther, Zahra, Emna, Gouider

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Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency by Ouardani, Cherifa, Elmahmoudi, Hejer, ELborgi, Wejden, Gharbi, Maroua, Meriem, Achour, Gouider, Emna

“…Congenital factor VII (FVII) deficiency is an autosomal recessive bleeding disorder characterized by a weak phenotypic and genotypic correlation. This study…”
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Molecular heterogeneity of factor XI deficiency in Tunisia by Gharbi, Maroua, Elmahmoudi, Hejer, ElBorgi, Wejden, Ouardani, Cherifa, Achour, Meriem, Gouider, Emna

“…Factor XI (FXI) deficiency is a rare inherited bleeding disorder that is highly prevalent in Ashkenazi Jewish ancestry but sporadically observed in most ethnic…”
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Molecular heterogeneity of factor XI deficiency in Tunisia by Gharbi, Maroua, Elmahmoudi, Hejer, ElBorgi, Wejden, Ouardani, Cherifa, Achour, Meriem, Gouider, Emna

“…Factor XI (FXI) deficiency is a rare inherited bleeding disorder that is highly prevalent in Ashkenazi Jewish ancestry but sporadically observed in most ethnic…”
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L’allo-immunisation anti-érythrocytaire en milieu obstétrical by Hachicha, Abir, Ben Jannet, Jamil, Salem, Sarra Fekih, Benlakhal, Fatma, Elborgi, Wejden, Gouider, Emna

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