H. Elmahmoudi

Factor VIII haplotypes frequencies in Tunisian hemophiliacs A

A. Elgaaied, H. Elmahmoudi, N. Belhedi, 2011, Diagnostic pathology.

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

H. Khodjet-el-khil, H. Elmahmoudi, A. Jlizi, 2012, Diagnostic Pathology.

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

H. Elmahmoudi, A. Jlizi, K. Zahra, 2012, Diagnostic Pathology.

The Glanzmann’s Thrombasthenia in Tunisia: A Cohort Study

H. Elmahmoudi, N. Belhedi, K. Zahra, 2017, Journal of hematology.

Low dose prophylaxis in Tunisian children with haemophilia

H. Elmahmoudi, K. Zahra, B. Meddeb, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Regional registry of bleeding disorders in Tunisia

H. Elmahmoudi, K. Zahra, B. Meddeb, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

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

Y. Lindqvist, A. Elgaaied, H. Elmahmoudi, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Molecular heterogeneity of factor XI deficiency in Tunisia

H. Elmahmoudi, E. Gouider, M. Gharbi, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency

H. Elmahmoudi, E. Gouider, M. Gharbi, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Identification of novel and recurrent mutations in Tunisian haemophilia B patients

H. Khodjet-el-khil, H. Elmahmoudi, A. Jlizi, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.