Faida Ouali

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

Chaîma Sahli, Amina Bibi, Faida Ouali et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2013 · 45 citations

Medicine, Genetics, Hematology +16

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia

Chaîma Sahli, Amina Bibi, Faida Ouali et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2013 · 27 citations

Medicine, Genetics, Hematology +17

First Description in Tunisia of a Point Mutation at Codon 119 (<i>C</i>CT→<i>T</i>CT) in the α1-Globin Gene: Hb Groene Hart in Association with the − α^3.7Deletion

Hajer Siala, Faida Ouali, Taïeb Messaoud et al. · Hemoglobin · 2005 · 15 citations

Life Sciences, Genetics, Hematology +15

A lower-cost protocol for sickle cell disease neonatal screening in Tunisia

Hajer Siala, Taboubi Neila, Hadj Fradj Sondess et al. · Annals of Saudi Medicine · 2012 · 13 citations · Full text

Medicine, Hematology, Preventive Medicine +16

Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia

Rim Belhaj Nefissi, Radhouene Doggui, Faida Ouali et al. · Hemoglobin · 2018 · 10 citations

Life Sciences, Genetics, Hematology +16