Low dose prophylaxis in Tunisian children with haemophilia von Gouider, E., Jouini, L., Achour, M., Elmahmoudi, H., Zahra, K., Saied, W., Meddeb, B.

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Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII von ELMAHMOUDI, H., WIGREN, E., LAATIRI, A., JLIZI, A., ELGAAIED, A., GOUIDER, E., LINDQVIST, Y.

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Regional registry of bleeding disorders in Tunisia von Elmahmoudi, H., Chalbi, A., Ben-Lakhal, F., Borji, W., Zahra, K., Zorgan, M., Meddeb, B., Gouider, E.

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Identification of novel and recurrent mutations in Tunisian haemophilia B patients von ELMAHMOUDI, H., KHODJET-EL-KHIL, H., BEN-AMOR, M., JLIZI, A., ZAHRA, K., MEDDEB, B., BEN-AMMAR- EL-GAAIED, A., GOUIDER, E.

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First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations von Elmahmoudi, Hejer, Khodjet-el-khil, Houssein, Wigren, Edvard, Jlizi, Asma, Zahra, Kaouther, Pellechia, Dorothé, Vinciguerra, Christine, Meddeb, Balkis, Elggaaied, Amel Ben Ammar, Gouider, Emna

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Identification of novel and recurrent mutations in Tunisian haemophilia B patients: LETTER TO THE EDITOR von ELMAHMOUDI, H., KHODJET-EL-KHIL, H., BEN-AMOR, M., JLIZI, A., ZAHRA, K., MEDDEB, B., BEN-AMMAR- EL-GAAIED, A., GOUIDER, E.

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