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Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia.

Diagn Pathol. 2012 Aug 8;7:92 | 01/08/2012
Elmahmoudi H, Ben-Lakhal F, Elborji W, Jlizi A, Zahra K, Sassi R, Zorgan M, Meddeb B, Elgaaied Ben Ammar A, Gouider E.

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First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations

Diagn Pathol. 2012 Aug 10;7:93. | 01/08/2012
Elmahmoudi H, Khodjet-el-khil H, Wigren E, Jlizi A, Zahra K, Pellechia D, Vinciguerra C, Meddeb B, Elggaaied AB, Gouider E.

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Creation and report of the Tunisian Fanconi Anemia Registry (TFAR)

Arch Pediatr. 2012 May;19(5):467-75 | 04/04/2012
S. Hadiji Mseddia,*, L. Kammouna, H. Bellaajb, Y. Ben Youssefc, L. Aissaouid, L. Torjemanee, F. Telmoudif, A. Amourig, H. Elghezalc, M. Ouedernie, Y. Ben Abdennebid, S. Hammemig, T. Ben Othmene, H. Ben Abidd, M. Bejaouie, S. Abdelhakf, M. Hachichaa, K. De

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Identification of a novel mutation in the MCFD2 gene in a Tunisian family with combined factor V and VIII deficiency.

LA TUNISIE MEDICALE - 2012 ; Vol 90 (n°04) | 01/04/2012
Hejer E, Adnen LM, Asma J, Ibtihel M, Benammar-Elgaaied A, Gouider E.

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Adult Gaucher disease in southern Tunisia: report of three cases.

Diagn Pathol.2012 Jan 10;7:4 | 01/01/2012
Ben Rhouma F1, Kallel F, Kefi R, Cherif W, Nagara M, Azaiez H, Jedidi I, Elloumi M, Abdelhak S, Mseddi S.

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