S. Fattoum

Variants in genetic modifiers of  -thalassemia can help to predict the major or intermedia type of the disease

Catherine Badens, Philippe Joly, Imane Agouti et al. · Haematologica · 2011 · 77 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease

Brahim Nsiri, Nasreddine Gritli, Fethi Bayoudh et al. · Hematology and Cell Therapy · 1996 · 71 citations

Medicine, Genetics, Hematology +10

β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians

S. Fattoum, Fethi Guémira, C. Öner et al. · Hemoglobin · 1991 · 58 citations

Medicine, Genetics, Hematology +15

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

Abi Ghanem, B Pothier, J Maréchal et al. · British Journal of Haematology · 1990 · 38 citations

Life Sciences, Genetics, Hematology +17

[Molecular epidemiology of cystic fibrosis in Tunisia].

T. Ben Messaoud, S Bel Haj Fredj, Afsha Bibi et al. · PubMed · 2006 · 29 citations

Life Sciences, Genetics, Molecular Genetics +17