Raouf Hafsia

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 17 publications

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Journal: Hemoglobin

Published: June 09, 2017

First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients.

First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients.

Journal: Hemoglobin

Published: November 11, 2016

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.

Journal: Hematology (Amsterdam, Netherlands)

Published: April 15, 2016

Monocentric study of Willebrand's disease in Tunisia: assets and difficulties.

Monocentric study of Willebrand's disease in Tunisia: assets and difficulties.

Journal: La Tunisie medicale

Published: February 20, 2016

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.

Journal: La Tunisie medicale

Published: September 17, 2015

Anti-erythrocyte and anti-HLA immunization in hemoglobinopathies

Anti-erythrocyte and anti-HLA immunization in hemoglobinopathies

Journal: Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine

Published: July 08, 2014

Measurement of d-dimers in non-valvular atrial fibrillation. First prospective Tunisian study

Measurement of d-dimers in non-valvular atrial fibrillation. First prospective Tunisian study

Journal: Annales de cardiologie et d'angeiologie

Published: April 10, 2014

Immunophenotyping of B chronic lymphoproliferative syndromes (CLL excluded): confrontation with the histology

Immunophenotyping of B chronic lymphoproliferative syndromes (CLL excluded): confrontation with the histology

Journal: Annales de biologie clinique

Published: December 18, 2013

Hemolytic auto immune anemia due do Ig A autoatibodies

Hemolytic auto immune anemia due do Ig A autoatibodies

Journal: La Tunisie medicale

Published: September 07, 2013

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia.

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia.

Journal: Polish journal of pathology : official journal of the Polish Society of Pathologists

Published: August 01, 2013

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients.

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients.

Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia

Published: March 19, 2013

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

Journal: Molecular biology reports

Published: December 02, 2012

Showing 1-12 of 17

Last Updated: 09/26/2026