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La Tunisie Medicale|May 1, 2008
[Cytology and immunophenotype features of hairy cell leukemia: 6 cases]Emna Gouider, Salah Naouel Ben, Wijden El Borgi, et al.La Tunisie Medicale|June 18, 2011
[Iron overload in sickle cell anemia : a study of 94 patients]Raouf Hafsia, Fatma Belakhal, Naouel Ben Salah, et al.La Tunisie Medicale|March 10, 2010
[Soluble tranferrin receptor in the biological diagnosis of iron deficiency. Report of 24 cases]Mohamed M Zorgati, Raouf Hafsia, Afef Bahlous, et al.La Tunisie Medicale|November 26, 2009
[Splenectomy in hereditary hemolytic anemia: 82 Tunisian cases]Raouf Hafsia, Sami Zriba, Emna Gouider, et al.La Tunisie Medicale|February 8, 2008
[Hemoglobin O Arab: about 20 cases]Raouf Hafsia, Emna Gouider, Sinda Ben Moussa, et al.Annales De Biologie Clinique|December 18, 2013
[Immunophenotyping of B chronic lymphoproliferative syndromes (CLL excluded): confrontation with the histology]Wijden El Borgi, Nawel Ben Salah, Fatma Ben Lakhal, et al.La Tunisie Medicale|September 17, 2015
Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patientsLeila Chaouch, Miniar Kalai, Dorra Chaouachi, et al.La Tunisie Medicale|February 20, 2016
Monocentric study of Willebrand's disease in Tunisia: assets and difficultiesFatma Ben Lakhal, Wijdene El Borgi, Emna Gouider, et al.La Tunisie Medicale|November 6, 2002
[Epidemiologic, clinical and cytohematologic characteristics of adult acute lymphoblastic leukemia in Tunisia]Moez Elloumi, Raouf Hafsia, Halima el Omri, et al.La Tunisie Medicale|April 27, 2010
[Thalassemia intermedia: 36 cases]Raouf Hafsia, Naouel Ben Salah, Emna Hafhouf, et al.Pageof 2