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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.

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.

Grossesse et accouchement chez une patiente porteuse d’une thrombasthénie de Glanzmann

LA TUNISIE MEDICALE - 2011 ; Vol 89 (n°12) : 951-2 | 01/12/2011
Anis Fadhlaoui, Naouel Ben Salah, Mohamed Khrouf, Moncef Boubaker, Emna Gouider, Fethi Zhioua, Anis Chaker

Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII.

Haemophilia. 2011Sep;17(5):e923-7 | 01/09/2011
H. ELMAHMOUDI, E. WIGREN, A. LAATIRI, A. JLIZI, A. ELGAAIED, E. GOUIDER and Y. LINDQVIST

Haematological and cytogenetic responses after only 7 days of Lenalidomide in a patient with myelodysplastic syndrome and chromosome 5q deletion

Leukemia Research 35 (2011) e175-e176 | 11/06/2011
Sondes Hadiji Mseddi ,Faten Kallel Olfa Kassar Moez Elloumi Department of Hematology, University of Sfax, HediChaker Hospital, Sfax, Tunisia Ines Jedidi Hematology Laboratory, Habib Bourguiba Hospital, Sfax, Tunisia