Publications

Home
/
Publications

Factor VIII haplotypes frequencies in Tunisian hemophiliacs A.

Diagnostic Pathology 2011,6:54 | 01/06/2011
Hejer Elmahmoudi, Nejla Belhedi, Asma Jlizi, Kaouther Zahra, Balkis Meddeb, Amel Ben Ammar Elgaaied and Emna Gouider

Identification of novel and recurrent mutations in Tunisian haemophilia B patients.

Haemophilia. 2011 May;17(3):544-5 | 01/05/2011
Elmahmoudi H, Khodjet-El-Khil H, Ben-Amor M, Jlizi A, Zahra K, Meddeb B, Ben-Ammar-El-Gaaied A, Gouider E.

Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency.

Haemophilia. 2010 Sep 1;16(5):801-4 | 01/09/2010
Abdallah HE, Gouider E, Amor MB, Jlizi A, Meddeb B, Elgaaied A.

Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency.

Blood Cells Mol Dis. 2010 Mar-Apr;44(2):120-3 | 01/04/2010
Abdallah HE, Gouider E, Stambouli N, Ben Amor M, Jlizi A, Belhedi N, Sassi R, Khodjetelkhil H, Meddeb B, Hafsia R, Hamza A, Elgaaied AB.

Small insertion (c.869insC) within F13A gene is dominant in Tunisian patients with inherited FXIII deficiency due to ancient founder effect.

Haemophilia. 2009 Sep;15(5):1176-9. | 01/09/2009
El Mahmoudi H, Amor MB, Gouider E, Horchani R, Hafsia R, Fadhlaoui K, Meddeb B, Hafsia A, Ammar El Gaaied AB.